sample_id stringlengths 1 3 | image_path stringlengths 12 14 | source dict | qa_by_category dict |
|---|---|---|---|
1 | images/1.png | {
"source_type": "Paper",
"source_name": "Nature Communications",
"source_doi": "https://doi.org/10.1038/s41467-022-30288-6",
"license": "CC-BY",
"year": "2022"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "ReactantSMILES",
"language": "en",
"question": "What is the SMILES representation of the reactant labeled '7'?",
"answer": "CC1(C)C=CC(=O)C2CCC(C=O)=CC21"
},
{
"question_id": "REI_Q2",
"su... |
2 | images/2.png | {
"source_type": "Paper",
"source_name": "Nature Communications",
"source_doi": "https://doi.org/10.1038/s41467-022-30288-6",
"license": "CC-BY",
"year": "2022"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "DieneIdentification",
"language": "en",
"question": "What conjugated diene is depicted on the left side of the reaction scheme?",
"answer": "Cyclopentadiene."
},
{
"question_id": "REI_Q2",
... |
3 | images/3.png | {
"source_type": "Paper",
"source_name": "Nature Communications",
"source_doi": "https://doi.org/10.1038/s41467-022-30288-6",
"license": "CC-BY",
"year": "2022"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "StarterUnits",
"language": "en",
"question": "What two CoA-derived building blocks are shown as the starting materials in the biosynthetic scheme?",
"answer": "Acetyl-CoA and Malonyl-CoA."
},
{
... |
4 | images/4.png | {
"source_type": "Paper",
"source_name": "Nature Communications",
"source_doi": "https://doi.org/10.1038/s41467-022-30288-6",
"license": "CC-BY",
"year": "2022"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "NamedCompound",
"language": "en",
"question": "What is the name of compound 1 shown in the scheme?",
"answer": "Sordaricin."
},
{
"question_id": "REI_Q2",
"subtype": "IntermediateLabel",
... |
5 | images/5.png | {
"source_type": "Paper",
"source_name": "Nature Communications",
"source_doi": "https://doi.org/10.1038/s41467-022-30288-6",
"license": "CC-BY",
"year": "2022"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "StartingCompound",
"language": "en",
"question": "What is the label of the starting compound shown on the left side of the scheme?",
"answer": "Compound 2."
},
{
"question_id": "REI_Q2",
"... |
6 | images/6.png | {
"source_type": "Paper",
"source_name": "Nature Communications",
"source_doi": "https://doi.org/10.1038/s41467-022-30288-6",
"license": "CC-BY",
"year": "2022"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is indicated above the reaction arrow in the scheme?",
"answer": "SdnH."
},
{
"question_id": "REI_Q2",
"subtype": "Cofact... |
7 | images/7.png | {
"source_type": "Paper",
"source_name": "Nature Communications",
"source_doi": "https://doi.org/10.1038/s41467-022-30288-6",
"license": "CC-BY",
"year": "2022"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "ReagentIdentification",
"language": "en",
"question": "Which oxidizing reagent is used in the first transformation?",
"answer": "Activated MnO2."
},
{
"question_id": "REI_Q2",
"subtype": "... |
8 | images/8.png | {
"source_type": "Paper",
"source_name": "Nature Communications",
"source_doi": "https://doi.org/10.1038/s41467-022-30288-6",
"license": "CC-BY",
"year": "2022"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "StartingCompoundLabel",
"language": "en",
"question": "What is the label of the starting compound shown on the left side of the scheme?",
"answer": "Compound 5 (shunt product)."
},
{
"question_i... |
9 | images/9.png | {
"source_type": "Paper",
"source_name": "Nature Communications",
"source_doi": "https://doi.org/10.1038/s41467-022-30288-6",
"license": "CC-BY",
"year": "2022"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "CatalysisType",
"language": "en",
"question": "What two types of processes are indicated above the reaction arrow?",
"answer": "Non-enzymatic (slow) or SdnG (slow)."
},
{
"question_id": "REI_Q2"... |
10 | images/10.png | {
"source_type": "Paper",
"source_name": "Nature Communications",
"source_doi": "https://doi.org/10.1038/s41467-022-30288-6",
"license": "CC-BY",
"year": "2022"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "SubstrateIdentification",
"language": "en",
"question": "What is the name of the substrate shown on the left side of the scheme?",
"answer": "Daidzein."
},
{
"question_id": "REI_Q2",
"subt... |
11 | images/11.png | {
"source_type": "Paper",
"source_name": "Research Square",
"source_doi": "https://doi.org/10.21203/rs.3.rs-2802333/v1",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "SubstrateLabel",
"language": "en",
"question": "What is the label of the alkene substrate shown on the left?",
"answer": "(Z)-1a."
},
{
"question_id": "REI_Q2",
"subtype": "DiazoReagent",
... |
12 | images/12.png | {
"source_type": "Paper",
"source_name": "Research Square",
"source_doi": "https://doi.org/10.21203/rs.3.rs-2802333/v1",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "AlkeneGeometry",
"language": "en",
"question": "What is the geometric configuration of substrate 1a in this scheme?",
"answer": "(E)-1a."
},
{
"question_id": "REI_Q2",
"subtype": "DiazoRea... |
13 | images/13.png | {
"source_type": "Paper",
"source_name": "Research Square",
"source_doi": "https://doi.org/10.21203/rs.3.rs-2802333/v1",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "SubstrateComposition",
"language": "en",
"question": "What is the geometric composition of substrate 1a in this reaction?",
"answer": "A Z/E mixture in a 1:1 ratio."
},
{
"question_id": "REI_Q2"... |
14 | images/14.png | {
"source_type": "Paper",
"source_name": "Research Square",
"source_doi": "https://doi.org/10.21203/rs.3.rs-2802333/v1",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "SubstrateType",
"language": "en",
"question": "What type of alkene substrate is shown on the left side of the scheme?",
"answer": "A Z/E mixture of an aryl-substituted alkene labeled (Z/E)-1."
},
{
... |
15 | images/15.png | {
"source_type": "Paper",
"source_name": "Research Square",
"source_doi": "https://doi.org/10.21203/rs.3.rs-2802333/v1",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "AlkeneGeometry",
"language": "en",
"question": "What is the geometric configuration of substrate 1a shown in this scheme?",
"answer": "(Z)-1a."
},
{
"question_id": "REI_Q2",
"subtype": "Ca... |
16 | images/16.png | {
"source_type": "Paper",
"source_name": "Research Square",
"source_doi": "https://doi.org/10.21203/rs.3.rs-2802333/v1",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "AlkeneGeometry",
"language": "en",
"question": "What is the geometric configuration of substrate 1a in this reaction?",
"answer": "(E)-1a."
},
{
"question_id": "REI_Q2",
"subtype": "Cataly... |
17 | images/17.png | {
"source_type": "Paper",
"source_name": "Research Square",
"source_doi": "https://doi.org/10.21203/rs.3.rs-2802333/v1",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "SubstrateIdentification",
"language": "en",
"question": "What protecting group is attached to the alkene substrate (Z/E)-1n?",
"answer": "OPiv (pivalate group)."
},
{
"question_id": "REI_Q2",
... |
18 | images/18.png | {
"source_type": "Paper",
"source_name": "Research Square",
"source_doi": "https://doi.org/10.21203/rs.3.rs-2802333/v1",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "SubstrateIdentification",
"language": "en",
"question": "What protecting group is present on substrate (Z/E)-1n?",
"answer": "An OPiv (pivalate) group."
},
{
"question_id": "REI_Q2",
"subt... |
19 | images/19.png | {
"source_type": "Paper",
"source_name": "Drug Design Development and Therapy",
"source_doi": "https://doi.org/10.2147/DDDT.S268796",
"license": "CC-BY-NC",
"year": "2020"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "SubstrateIdentification",
"language": "en",
"question": "What is the name of the parent drug shown on the left side of the scheme?",
"answer": "Sildenafil."
},
{
"question_id": "REI_Q2",
"... |
20 | images/20.png | {
"source_type": "Paper",
"source_name": "Molecules",
"source_doi": "https://doi.org/10.3390/molecules22091422",
"license": "CC-BY",
"year": "2017"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "PrecursorIdentification",
"language": "en",
"question": "What are the two isoprenoid precursors shown on the left side of the pathway?",
"answer": "Isopentenyl pyrophosphate (IPP) and dimethylallyl pyrophosph... |
21 | images/21.png | {
"source_type": "Paper",
"source_name": "Journal of Ginseng Research",
"source_doi": "https://doi.org/10.1016/j.jgr.2018.02.005",
"license": "CC-BY-NC-ND",
"year": "2019"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "InitialSubstrate",
"language": "en",
"question": "What is the starting compound shown at the top left of the pathway?",
"answer": "Squalene."
},
{
"question_id": "REI_Q2",
"subtype": "Firs... |
22 | images/22.png | {
"source_type": "Paper",
"source_name": "Plants",
"source_doi": "https://doi.org/10.3390/plants13182602",
"license": "CC-BY",
"year": "2024"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "StartingSubstrates",
"language": "en",
"question": "Which two amino acids are shown as initial substrates in the pathway?",
"answer": "Phenylalanine (Phe) and Tyrosine (Tyr)."
},
{
"question_id"... |
23 | images/23.png | {
"source_type": "Paper",
"source_name": "Plants",
"source_doi": "https://doi.org/10.3390/plants13182602",
"license": "CC-BY",
"year": "2024"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "SubstrateIdentification",
"language": "en",
"question": "What is the substrate shown on the left side of the scheme?",
"answer": "Resveratrol."
},
{
"question_id": "REI_Q2",
"subtype": "Pr... |
24 | images/24.png | {
"source_type": "Paper",
"source_name": "Plants",
"source_doi": "https://doi.org/10.3390/plants13182602",
"license": "CC-BY",
"year": "2024"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "InitialSubstrate",
"language": "en",
"question": "What is the initial substrate in the first reaction step?",
"answer": "Resveratrol."
},
{
"question_id": "REI_Q2",
"subtype": "Intermediat... |
25 | images/25.png | {
"source_type": "Paper",
"source_name": "Frontiers in Bioengineering and Biotechnology",
"source_doi": "https://doi.org/10.3389/fbioe.2022.1109929",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "InitialSubstrate",
"language": "en",
"question": "What is the initial substrate shown on the left side of the pathway?",
"answer": "L-Tryptophan."
},
{
"question_id": "REI_Q2",
"subtype": ... |
26 | images/26.png | {
"source_type": "Paper",
"source_name": "Frontiers in Bioengineering and Biotechnology",
"source_doi": "https://doi.org/10.3389/fbioe.2022.1109929",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "InitialSubstrate",
"language": "en",
"question": "What is the starting substrate in this pathway?",
"answer": "6-bromo-tryptophan."
},
{
"question_id": "REI_Q2",
"subtype": "IntermediateId... |
27 | images/27.png | {
"source_type": "Paper",
"source_name": "Frontiers in Bioengineering and Biotechnology",
"source_doi": "https://doi.org/10.3389/fbioe.2022.1109929",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "InitialSubstrate",
"language": "en",
"question": "What is the initial compound at the beginning of the pathway?",
"answer": "Indole."
},
{
"question_id": "REI_Q2",
"subtype": "Intermediate... |
28 | images/28.png | {
"source_type": "Paper",
"source_name": "Frontiers in Bioengineering and Biotechnology",
"source_doi": "https://doi.org/10.3389/fbioe.2022.1109929",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "InitialCompound",
"language": "en",
"question": "What is the starting compound in this reaction sequence?",
"answer": "2,3-Dihydroxyindole."
},
{
"question_id": "REI_Q2",
"subtype": "Secon... |
29 | images/29.png | {
"source_type": "Paper",
"source_name": "Frontiers in Bioengineering and Biotechnology",
"source_doi": "https://doi.org/10.3389/fbioe.2022.1109929",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "InitialCompound",
"language": "en",
"question": "What is the starting compound in this sequence?",
"answer": "6-Br-2,3-dihydroxyindole."
},
{
"question_id": "REI_Q2",
"subtype": "SecondInt... |
30 | images/30.png | {
"source_type": "Paper",
"source_name": "Frontiers in Bioengineering and Biotechnology",
"source_doi": "https://doi.org/10.3389/fbioe.2022.1109929",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "RightmostCompound",
"language": "en",
"question": "What compound is shown on the rightmost side of the scheme?",
"answer": "6-Br-isatin."
},
{
"question_id": "REI_Q2",
"subtype": "MiddleCo... |
31 | images/31.png | {
"source_type": "Paper",
"source_name": "Frontiers in Bioengineering and Biotechnology",
"source_doi": "https://doi.org/10.3389/fbioe.2022.1109929",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "LeftmostProduct",
"language": "en",
"question": "What compound is shown on the far left of the scheme?",
"answer": "6-Br-catechol."
},
{
"question_id": "REI_Q2",
"subtype": "CentralInterme... |
32 | images/32.png | {
"source_type": "Paper",
"source_name": "Frontiers in Bioengineering and Biotechnology",
"source_doi": "https://doi.org/10.3389/fbioe.2022.1109929",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "UpperPathwaySubstrate",
"language": "en",
"question": "What is the starting substrate in the upper pathway?",
"answer": "L-Tryptophan."
},
{
"question_id": "REI_Q2",
"subtype": "UpperInter... |
33 | images/33.png | {
"source_type": "Paper",
"source_name": "Analytical Science Advances",
"source_doi": "https://doi.org/10.1002/ansa.202300058",
"license": "CC-BY-NC-ND",
"year": "2024"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "SubstrateIdentification",
"language": "en",
"question": "What is the name of the starting compound shown on the left?",
"answer": "TX101."
},
{
"question_id": "REI_Q2",
"subtype": "Reactio... |
34 | images/34.png | {
"source_type": "Paper",
"source_name": "PLOS ONE",
"source_doi": "https://doi.org/10.1371/journal.pone.0115590",
"license": "CC-BY",
"year": "2014"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "StartingCompound",
"language": "en",
"question": "What is the name of the starting compound shown on the left?",
"answer": "D4-AcAP."
},
{
"question_id": "REI_Q2",
"subtype": "ProductIdent... |
35 | images/35.png | {
"source_type": "Paper",
"source_name": "PLOS ONE",
"source_doi": "https://doi.org/10.1371/journal.pone.0115590",
"license": "CC-BY",
"year": "2014"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "StartingCompound",
"language": "en",
"question": "What is the name of the starting compound in the reaction sequence?",
"answer": "NANL."
},
{
"question_id": "REI_Q2",
"subtype": "Intermed... |
36 | images/36.png | {
"source_type": "Paper",
"source_name": "PLOS ONE",
"source_doi": "https://doi.org/10.1371/journal.pone.0115590",
"license": "CC-BY",
"year": "2014"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "StartingCompound",
"language": "en",
"question": "What is the starting compound in this reaction sequence?",
"answer": "noroline."
},
{
"question_id": "REI_Q2",
"subtype": "IntermediateIde... |
37 | images/37.png | {
"source_type": "Paper",
"source_name": "PLOS ONE",
"source_doi": "https://doi.org/10.1371/journal.pone.0115590",
"license": "CC-BY",
"year": "2014"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "StartingCompound",
"language": "en",
"question": "What is the starting compound shown in panel E?",
"answer": "noroline."
},
{
"question_id": "REI_Q2",
"subtype": "IntermediateIdentificati... |
38 | images/38.png | {
"source_type": "Paper",
"source_name": "PLOS ONE",
"source_doi": "https://doi.org/10.1371/journal.pone.0115590",
"license": "CC-BY",
"year": "2014"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "StartingCompound",
"language": "en",
"question": "What is the starting compound in this reaction?",
"answer": "loline."
},
{
"question_id": "REI_Q2",
"subtype": "ProductIdentification",
... |
39 | images/39.png | {
"source_type": "Paper",
"source_name": "PLOS ONE",
"source_doi": "https://doi.org/10.1371/journal.pone.0115590",
"license": "CC-BY",
"year": "2014"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "ReactantIdentification",
"language": "en",
"question": "What are the two starting reactants shown in the scheme?",
"answer": "L-Pro and O-acetylhomoserine."
},
{
"question_id": "REI_Q2",
"... |
40 | images/40.png | {
"source_type": "Paper",
"source_name": "PLOS ONE",
"source_doi": "https://doi.org/10.1371/journal.pone.0115590",
"license": "CC-BY",
"year": "2014"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "CompoundIdentification",
"language": "en",
"question": "What three compounds are shown in this scheme?",
"answer": "loline, noroline, and N-acetylnoroline (NANL)."
},
{
"question_id": "REI_Q2",
... |
41 | images/41.png | {
"source_type": "Paper",
"source_name": "PLOS ONE",
"source_doi": "https://doi.org/10.1371/journal.pone.0115590",
"license": "CC-BY",
"year": "2014"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "StartingCompound",
"language": "en",
"question": "What is the starting compound shown on the left?",
"answer": "N-methylloline (NML)."
},
{
"question_id": "REI_Q2",
"subtype": "ProductIden... |
42 | images/42.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is labeled as catalyzing the transformations in this scheme?",
"answer": "CYP107H1."
},
{
"question_id": "REI_Q2",
"subty... |
43 | images/43.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is labeled above the reaction arrow?",
"answer": "CYP107A1."
},
{
"question_id": "REI_Q2",
"subtype": "FunctionalGroupCha... |
44 | images/44.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is indicated above the reaction arrow?",
"answer": "CYP107U1."
},
{
"question_id": "REI_Q2",
"subtype": "FunctionalGroupC... |
45 | images/45.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is indicated as catalyzing the reaction?",
"answer": "CYP107L1."
},
{
"question_id": "REI_Q2",
"subtype": "FunctionalGrou... |
46 | images/46.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is labeled as catalyzing the transformation?",
"answer": "CYP107L1."
},
{
"question_id": "REI_Q2",
"subtype": "Functional... |
47 | images/47.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is indicated as catalyzing the reaction?",
"answer": "CYP107L1."
},
{
"question_id": "REI_Q2",
"subtype": "FunctionalGrou... |
48 | images/48.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is shown above the reaction arrow?",
"answer": "CYP107L1."
},
{
"question_id": "REI_Q2",
"subtype": "FunctionalGroupIntro... |
49 | images/49.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is labeled above the reaction arrow?",
"answer": "CYP107L1."
},
{
"question_id": "REI_Q2",
"subtype": "FunctionalGroupInt... |
50 | images/50.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is labeled as catalyzing the transformation?",
"answer": "CYP107L1."
},
{
"question_id": "REI_Q2",
"subtype": "Functional... |
51 | images/51.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is shown above both reaction arrows?",
"answer": "CYP107BR1."
},
{
"question_id": "REI_Q2",
"subtype": "FunctionalGroupIn... |
52 | images/52.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is indicated above the reaction arrow?",
"answer": "CYP107B."
},
{
"question_id": "REI_Q2",
"subtype": "FunctionalGroupIn... |
53 | images/53.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is shown as catalyzing the transformation?",
"answer": "CYP107C1."
},
{
"question_id": "REI_Q2",
"subtype": "FunctionalGr... |
54 | images/54.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is indicated above the reaction arrow?",
"answer": "CYP107G1."
},
{
"question_id": "REI_Q2",
"subtype": "FunctionalGroupI... |
55 | images/55.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is labeled as catalyzing the transformation?",
"answer": "CYP107E6."
},
{
"question_id": "REI_Q2",
"subtype": "Functional... |
56 | images/56.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is indicated as catalyzing the reaction?",
"answer": "CYP107W1."
},
{
"question_id": "REI_Q2",
"subtype": "FunctionalGrou... |
57 | images/57.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is shown to catalyze the reaction?",
"answer": "CYP107Z14."
},
{
"question_id": "REI_Q2",
"subtype": "FunctionalGroupChan... |
58 | images/58.png | {
"source_type": "Paper",
"source_name": "Biomolecules",
"source_doi": "https://doi.org/10.3390/biom13121733",
"license": "CC-BY",
"year": "2023"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "EnzymeIdentification",
"language": "en",
"question": "Which enzyme is indicated as catalyzing the transformation?",
"answer": "CYP107X1."
},
{
"question_id": "REI_Q2",
"subtype": "Function... |
59 | images/59.png | {
"source_type": "Paper",
"source_name": "AMB Express",
"source_doi": "https://doi.org/10.1186/s13568-020-01064-w",
"license": "CC-BY",
"year": "2020"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "SubstrateName",
"language": "en",
"question": "What is the name of the substrate shown on the left side of the reaction?",
"answer": "Cyclophosphamide (CPA)."
},
{
"question_id": "REI_Q2",
... |
60 | images/60.png | {
"source_type": "Paper",
"source_name": "International Journal of Molecular Sciences",
"source_doi": "https://doi.org/10.3390/ijms150610271",
"license": "CC-BY",
"year": "2014"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "StartingCompound",
"language": "en",
"question": "What is the starting compound labeled at the left of the scheme?",
"answer": "3-nitrobenzanthrone (3-NBA)."
},
{
"question_id": "REI_Q2",
... |
61 | images/61.png | {
"source_type": "Paper",
"source_name": "International Journal of Molecular Sciences",
"source_doi": "https://doi.org/10.3390/ijms150610271",
"license": "CC-BY",
"year": "2014"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "ParentCompound",
"language": "en",
"question": "What is the primary compound shown at the top center of the activation pathway?",
"answer": "Aristolochic acid I (AAI)."
},
{
"question_id": "REI_... |
62 | images/62.png | {
"source_type": "Paper",
"source_name": "International Journal of Molecular Sciences",
"source_doi": "https://doi.org/10.3390/ijms150610271",
"license": "CC-BY",
"year": "2014"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "StartingFunctionalGroup",
"language": "en",
"question": "Which functional group is reduced in step 1 of the scheme?",
"answer": "The nitro (–NO2) group."
},
{
"question_id": "REI_Q2",
"sub... |
63 | images/63.png | {
"source_type": "Paper",
"source_name": "Chemical Research in Toxicology",
"source_doi": "https://doi.org/10.1021/tx300201p",
"license": "All rights reserved",
"year": "2012"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "ParentCompound",
"language": "en",
"question": "What is the parent polycyclic aromatic hydrocarbon shown at the beginning of the scheme?",
"answer": "Benzo[a]pyrene (B[a]P)."
},
{
"question_id":... |
64 | images/64.png | {
"source_type": "Paper",
"source_name": "Chemical Research in Toxicology",
"source_doi": "https://doi.org/10.1021/tx300201p",
"license": "All rights reserved",
"year": "2012"
} | {
"ReactionElementIdentification": [
{
"question_id": "REI_Q1",
"subtype": "ParentCompound",
"language": "en",
"question": "What is the parent compound shown at the left of the scheme?",
"answer": "Benzo[a]pyrene (B[a]P)."
},
{
"question_id": "REI_Q2",
"subtype": ... |
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