prompt large_string | completion string | metadata dict |
|---|---|---|
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:104:a_to_b",
"pair_id": "9:104:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "104",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:119:a_to_b",
"pair_id": "9:119:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "119",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:129:a_to_b",
"pair_id": "9:129:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "129",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:226:a_to_b",
"pair_id": "9:226:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "226",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:337:a_to_b",
"pair_id": "9:337:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "337",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:398:a_to_b",
"pair_id": "9:398:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "398",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:423:a_to_b",
"pair_id": "9:423:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "423",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:464:a_to_b",
"pair_id": "9:464:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "464",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:502:a_to_b",
"pair_id": "9:502:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "502",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:503:a_to_b",
"pair_id": "9:503:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "503",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:681:a_to_b",
"pair_id": "9:681:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "681",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:688:a_to_b",
"pair_id": "9:688:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "688",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:711:a_to_b",
"pair_id": "9:711:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "711",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:712:a_to_b",
"pair_id": "9:712:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "712",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:717:a_to_b",
"pair_id": "9:717:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "717",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:724:a_to_b",
"pair_id": "9:724:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "724",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:770:a_to_b",
"pair_id": "9:770:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "770",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:802:a_to_b",
"pair_id": "9:802:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "802",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:835:a_to_b",
"pair_id": "9:835:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "835",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:840:a_to_b",
"pair_id": "9:840:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "840",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:881:a_to_b",
"pair_id": "9:881:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "881",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:980:a_to_b",
"pair_id": "9:980:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "980",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical_sm... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:1012:a_to_b",
"pair_id": "9:1012:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "1012",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:1026:a_to_b",
"pair_id": "9:1026:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "1026",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:1032:a_to_b",
"pair_id": "9:1032:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "1032",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:1046:a_to_b",
"pair_id": "9:1046:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "1046",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:1119:a_to_b",
"pair_id": "9:1119:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "1119",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:1285:a_to_b",
"pair_id": "9:1285:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "1285",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:1400:a_to_b",
"pair_id": "9:1400:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "1400",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:1551:a_to_b",
"pair_id": "9:1551:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "1551",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:1748:a_to_b",
"pair_id": "9:1748:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "1748",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:1786:a_to_b",
"pair_id": "9:1786:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "1786",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:1897:a_to_b",
"pair_id": "9:1897:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "1897",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:1930:a_to_b",
"pair_id": "9:1930:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "1930",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:1936:a_to_b",
"pair_id": "9:1936:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "1936",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:1989:a_to_b",
"pair_id": "9:1989:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "1989",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:2011:a_to_b",
"pair_id": "9:2011:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2011",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:2077:a_to_b",
"pair_id": "9:2077:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2077",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:2155:a_to_b",
"pair_id": "9:2155:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2155",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:2156:a_to_b",
"pair_id": "9:2156:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2156",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:2186:a_to_b",
"pair_id": "9:2186:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2186",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:2300:a_to_b",
"pair_id": "9:2300:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2300",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:2367:a_to_b",
"pair_id": "9:2367:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2367",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:2371:a_to_b",
"pair_id": "9:2371:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2371",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:2544:a_to_b",
"pair_id": "9:2544:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2544",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:2569:a_to_b",
"pair_id": "9:2569:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2569",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:2620:a_to_b",
"pair_id": "9:2620:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2620",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:2625:a_to_b",
"pair_id": "9:2625:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2625",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:2633:a_to_b",
"pair_id": "9:2633:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2633",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:2662:a_to_b",
"pair_id": "9:2662:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2662",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:2857:a_to_b",
"pair_id": "9:2857:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2857",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:2891:a_to_b",
"pair_id": "9:2891:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2891",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:2913:a_to_b",
"pair_id": "9:2913:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "2913",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:3097:a_to_b",
"pair_id": "9:3097:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "3097",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:3101:a_to_b",
"pair_id": "9:3101:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "3101",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:3189:a_to_b",
"pair_id": "9:3189:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "3189",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:3272:a_to_b",
"pair_id": "9:3272:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "3272",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:3292:a_to_b",
"pair_id": "9:3292:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "3292",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:3305:a_to_b",
"pair_id": "9:3305:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "3305",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | A | {
"sample_id": "9:3321:a_to_b",
"pair_id": "9:3321:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "3321",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:3440:a_to_b",
"pair_id": "9:3440:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "3440",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
You are comparing two molecules for oral bioavailability.
Oral bioavailability (F, %) is the fraction of an orally administered dose reaching systemic circulation unchanged (0–100%), governed by intestinal absorption (solubility, permeability) and first-pass gut/hepatic metabolism; it is species- and dose-dependent.
... | B | {
"sample_id": "9:3526:a_to_b",
"pair_id": "9:3526:a_to_b",
"split": "train",
"split_version": "oral_bioavailability_shared_eval_directed_v2",
"eval_subset": null,
"group_id": null,
"record_id_a": "9",
"record_id_b": "3526",
"canonical_smiles_a": "Cc1coc2c1C(=O)C(=O)c1c-2ccc2c1CCCC2(C)C",
"canonical... |
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