Codemaster67/Unichem_chemabs_10M_tokens
Updated • 113
text stringlengths 3 4.59k | source stringclasses 2
values | num_tokens int64 1 1.21k |
|---|---|---|
CCOC(=O)C(C#N)=C(S)Nc1ccc(C#N)cc1 | unichem_smiles | 27 |
CN=C(O)C1(c2cncc(-c3ccc4c(c3)CCC(=O)N4C)c2)CC1 | unichem_smiles | 37 |
COC(=O)c1oc(-c2ccccc2)c(O)c1O | unichem_smiles | 23 |
CN1CCN(c2ccc(N=C(O)C3CC(=O)N(CC(F)(F)F)C3)cc2Cl)CC1 | unichem_smiles | 41 |
O=C(O)c1c[nH]nc1-c1cccc2cnccc12 | unichem_smiles | 23 |
OCC1OC(n2cnc3c(O)ncnc32)C(O)C1O.[Na] | unichem_smiles | 28 |
N=C(O)c1ccccc1N=C(O)CSc1cccc(NC(=O)C(=Cc2ccc([N+](=O)[O-])cc2)N=C(O)c2ccccc2)c1 | unichem_smiles | 61 |
O=S(O)NCc1ccc(-c2nsc(N=C(O)N(CCc3ccccn3)CCC(c3ccc(F)cc3)c3ccc(F)cc3)n2)cc1 | unichem_smiles | 56 |
CNCC(OCCOCCOC)c1cccc(OC)c1 | unichem_smiles | 17 |
CN=c1nc(Nc2ccc(OC(C)C)cc2)[nH]c(OC)n1 | unichem_smiles | 29 |
CCCCCCn1cc(CCCN=C(O)[C@H]2CC(=O)O[C@@]23CCOC(C)(C)C3)c2ccccc21 | unichem_smiles | 44 |
Impact of replacing Bis-GMA and TEGDMA by other commercially available monomers on the properties of resin-based composites. Impact of replacing Bis-GMA and TEGDMA by other commercially available monomers on the properties of resin-based composites. <h4>Purpose</h4>To evaluate important material properties of six exper... | chemabs | 348 |
Cc1cc(C(=O)Nc2ccc(Oc3ccc(Cl)cc3)cc2)c(N)nc1C | unichem_smiles | 35 |
CCCCCCCCCCCCCCCCCC[C@H](C)C[C@H](C)/C=C(\C)C(=O)O[C@H]1[C@@H](O[C@H]2O[C@H](COC(=O)/C(C)=C/[C@@H](C)C[C@@H](C)CCCCCCCCCCCCCCCC)[C@@H](O)[C@H](OC(=O)[C@@H](C)[C@@H](O)[C@@H](C)C[C@@H](C)CCCCCCCCCCCCCCCCCC)[C@H]2OC(=O)CCCCCCCCCCCCCCC)O[C@H](CO)[C@@H](OC(=O)/C(C)=C/[C@@H](C)C[C@@H](C)CCCCCCCCCCCCCCCCCC)[C@@H]1O | unichem_smiles | 198 |
Cc1nc[nH]c1CN1CC(=O)N(C(C)C)C[C@H](OCc2ccc(F)cc2)C1 | unichem_smiles | 43 |
CC[C@@H](C)[C@H](N=C(O)[C@@H](N=C(O)CCCOc1cccc(OCCCC(O)=N[C@H](C(O)=N[C@H](C(O)=N[C@H](C(=O)OC)C(C)C)[C@H](C)CC)[C@H](C)O)n1)[C@H](C)O)C(O)=N[C@H](C(=O)OC)C(C)C | unichem_smiles | 127 |
CCOC(=O)c1c([NH+]=C(O)C(C)C)sc2c1CC(C)(C)NC2(C)C | unichem_smiles | 39 |
Cc1ccc(Oc2c(C)cccc2Cl)c(CC(=O)O)c1 | unichem_smiles | 27 |
COc1cc(C)cc(C)c1S(=O)(=O)N[C@H](CN)C1CC1 | unichem_smiles | 33 |
VAV proteins as signal integrators for multi-subunit immune-recognition receptors. VAV proteins as signal integrators for multi-subunit immune-recognition receptors. In recent years, substantial progress has been made towards the identification of intracellular signalling molecules that couple multi-subunit immune-reco... | chemabs | 171 |
Cc1nn(C(C)(C)C)cc1C(C)N=C(O)Nc1ccc(CN2CCOC2=O)cc1 | unichem_smiles | 40 |
Impact of using stored cells for immunofluorescence detection of antiperinuclear factor on sensitivity of the method for the diagnosis of rheumatoid arthritis. Impact of using stored cells for immunofluorescence detection of antiperinuclear factor on sensitivity of the method for the diagnosis of rheumatoid arthritis. ... | chemabs | 318 |
Cc1cc(C(=O)NC2CCCC2)ccc1NC(=O)C(C)N1CCC(C(O)=Nc2cccc(C(O)=Nc3ccc(F)cc3F)c2)CC1 | unichem_smiles | 59 |
C=CC(=O)OCCOc1cc(-c2ccc(C3=CCCCC3)cc2)ccc1CCCO | unichem_smiles | 32 |
Br.CC(C)N(c1ccc2nc3ccc(NCC[N-]C(=O)OC(C)(C)C)cc3[s+]c2c1)C(C)C.O=C(O)C(F)(F)F | unichem_smiles | 65 |
PREPARATION OF AROMATIC ORGANOZINC COMPOUNDS AND COMPOSITION THEREFOR PREPARATION OF AROMATIC ORGANOZINC COMPOUNDS AND COMPOSITION THEREFOR The invention concerns a technique for preparing aromatic organozinc compounds and a composition therefor. Said composition consists in a reagent capable of synthesizing organozinc... | chemabs | 127 |
CC(C)[C@H](CN=C(O)[C@H](C)N=C(O)c1ccoc1)c1ccccc1 | unichem_smiles | 37 |
CCc1oc2ccccc2c1CNCc1ccc(N(C)C(=O)c2ccncc2)cc1 | unichem_smiles | 34 |
CCN=C(O)CN=C(O)CS(=O)(=O)N1CCN(c2cccc(C)c2)CC1 | unichem_smiles | 37 |
CC1(C(O)=NC2(CO)CC2)CCCC1 | unichem_smiles | 17 |
CN(Cc1ccccc1)C(=O)c1cccc(CN=[N+]=[N-])c1 | unichem_smiles | 29 |
COc1ccc(OC)c2sc(N(Cc3cccnc3)C(=O)CCCSCc3ccccc3)nc12 | unichem_smiles | 35 |
Cc1ccc(F)cc1C1CCN1 | unichem_smiles | 14 |
Positive and negative regulation of carbon nanotube catalysts through encapsulation within macrocycles. Positive and negative regulation of carbon nanotube catalysts through encapsulation within macrocycles. One of the most attractive applications of carbon nanomaterials is as catalysts, due to their extreme surface-to... | chemabs | 247 |
CC(C)(C)c1ccc(N=C(O)CCN=C(O)[C@H](CCOOOP=O)CC(=O)CCCCCN2C(=O)C=CC2=O)cc1[N+](=O)[O-] | unichem_smiles | 65 |
O=C(O)[C@H](CCS)N=C(O)c1c(O)ccc2ccccc12 | unichem_smiles | 30 |
CC1CC(NC(=O)c2ccc(C#N)cc2)CCN1Cc1ccccc1 | unichem_smiles | 29 |
O=C(O)COc1cn(-c2ccc(F)cc2)c2ccc(Cl)cc12 | unichem_smiles | 28 |
Cc1cc(C)c(C(=O)N=c2ccccn2Cc2ccccc2)o1 | unichem_smiles | 30 |
CC(Oc1ccc(C=C2SC(=S)N(c3cccc(Cl)c3)C2=O)cc1)C(=O)O | unichem_smiles | 41 |
CCC1CC(C)C(C)C2CCC3C2C1(C)C3(C)CC | unichem_smiles | 27 |
Nc1ccc2oc(=NCC3CCCC3CO)[nH]c2c1 | unichem_smiles | 22 |
[N-]=[N+]=NC(=O)c1ccc(COc2ccc(Cl)cc2Cl)cc1 | unichem_smiles | 30 |
COC(=O)c1csc(N=C(O)c2cccc(C)c2Cl)c1C | unichem_smiles | 30 |
COc1ccc(N2CCN(CCC3CC4(CCCCC4)C(=O)O3)CC2)cc1 | unichem_smiles | 32 |
Cl.OC(=Nc1nccs1)[C@H]1C[C@@H](O)CN1 | unichem_smiles | 28 |
Cc1cc(Oc2c(F)cc(COc3cc4n(c(=O)n3)CC3COCN43)cc2F)ccn1 | unichem_smiles | 43 |
Cc1[nH+]n(-c2ccccc2)c(N2CCN(C)CC2)c1CN(CC(C)C)C(=O)[C@H](C)Cl | unichem_smiles | 50 |
c1cc2c(s1)-c1c(ccc3c4c(ccc13)Cc1ccsc1-4)C2 | unichem_smiles | 33 |
Cc1sc2ncn(C(C)C(=O)c3ccc4c(c3)N=C(O)CO4)c(=O)c2c1C | unichem_smiles | 45 |
CCCC1(CN=C(O)CN2C(=O)CSc3ccccc32)CC1 | unichem_smiles | 25 |
COC(=O)C(O)c1cccc(O)c1Cl | unichem_smiles | 19 |
COc1ccc2c(c1)c(/C=C1\Oc3cc(OCc4ccc(F)cc4Cl)cc(C)c3C1=O)cn2C | unichem_smiles | 47 |
COc1ccsc1S(=O)(=O)NCc1ccccc1CN1CCC(C)CC1 | unichem_smiles | 28 |
COCCn1c(CN2CCC(c3cccc4c3OC(C)(c3ccccc3)O4)CC2)nc2ccc(C(=O)O)cc21.O=CO | unichem_smiles | 49 |
Cc1cc2c(=O)n(-c3ccccc3)c(=O)n(CCCC(=O)[O-])c2s1 | unichem_smiles | 37 |
CN(C)C(=O)C1C2C=CC3(CN(CCN4CCCCC4)C(=O)C13)O2 | unichem_smiles | 37 |
O=C(CC1CCCC(O)=N1)N1CCOC(C2CCC2)C1 | unichem_smiles | 25 |
Cn1ncnc1CNC(=O)C(=O)N1CCc2c1cccc2C(F)(F)F | unichem_smiles | 33 |
Cc1c[nH]c(=N)[nH]c1=Nc1c(F)c(F)c(F)c(F)c1F | unichem_smiles | 41 |
CC(C)(C)OC(=O)CN1CCN(CC(=O)OC(C)(C)C)CCN(CC(O)=N[C@@H](CSOOO)C(O)=NCCNS(=O)(=O)c2ccc(-c3ccc(S(=O)(=O)N[C@@H](CN=C(O)c4ccc5c(cnn5CCCN=c5[nH]cc[nH]5)c4)C(=O)O)cc3)cc2)CCN(CC(=O)OC(C)(C)C)CC1 | unichem_smiles | 147 |
COc1c(-c2ccc3ccccc3c2)cc(CCC(=O)O)cc1[N+](=O)[O-] | unichem_smiles | 36 |
COCCCN=C(O)c1cncc(N2CCc3ccccc32)c1 | unichem_smiles | 24 |
COc1ccc(CN=C(O)Cc2c(C)nc3c4ccccc4nn3c2C)cc1OC | unichem_smiles | 34 |
CC(C)C(O)=Nc1ccc2c(c1)C(=O)N(C)[C@H]1CC[C@@H](CC(O)=NCc3ccccc3F)O[C@@H]1CO2 | unichem_smiles | 59 |
CC(C)C(C)C(C#N)c1ccccc1 | unichem_smiles | 19 |
CC(=O)c1cccc(N=C(O)CN2C(=O)CCc3cc(S(=O)(=O)N4CCCCC4C)ccc32)c1 | unichem_smiles | 47 |
CC12[n+]3ccc4ccccc4c3C[N+]1(CCc1ccc(S(N)(=O)=O)cc1)Cc1c3ccccc3cc[n+]12 | unichem_smiles | 52 |
CCC[C@H](c1nnnn1C1CCCC1)N(Cc1ccco1)Cc1cc2cccc(C)c2nc1O | unichem_smiles | 39 |
CCn1ncnc1C(=O)N1CCN(C(=O)c2cccc(C3CC3)c2)C[C@@H]1C | unichem_smiles | 41 |
COc1cc(C2=NN(C(=O)c3ccccc3)[C@H](Cc3ccccc3)C2)c(C)cc1OCC(=O)O | unichem_smiles | 48 |
[N-]=[N+]=Nc1cc(Cl)cc2c3ccncc3n(CC(F)(F)F)c12 | unichem_smiles | 35 |
CCC(N)(C(CC(=O)N1CCCNCC1)N=[N+]=[N-])[Si](C)(C)C | unichem_smiles | 35 |
Cc1ccc2c(c1)C(NC(=O)C(=O)Nc1ccc(N=C(O)C3CC3)nc1)CCC2 | unichem_smiles | 43 |
c1ccc(COCC2OC3(CCC4(CC4)O3)CC3C(OCc4ccccc4)C23OCc2ccccc2)cc1 | unichem_smiles | 41 |
O=C1N=C2C(=C(C3CCNCC3)NN2C(c2ccccc2)c2ccccc2)[C@@H](C(F)(F)F)[C@H]1O | unichem_smiles | 54 |
CC(C)C(Sc1cccc(O)c1)C(O)=NCC1CCCO1 | unichem_smiles | 25 |
CCCCN(C(=O)Cn1nnc2ccccc21)[C@H](C(O)=NC1CCCC1)c1cc(OC)ccc1OC | unichem_smiles | 40 |
Cc1c(C=O)c2ccccn2c1[C@]1(c2ccc(Cl)c([N+](=O)[O-])c2)N[C@@H](C)Cc2ccc(F)c(Br)c21 | unichem_smiles | 63 |
CSc1nc(-c2ccc([N+](=O)[O-])c(C)c2)[nH]c(=N)n1 | unichem_smiles | 35 |
COCCCN=C(O)NN=C(O)Cc1c(C)cc(C)cc1C | unichem_smiles | 28 |
COc1ccc(Cl)cc1N1CCC(N=C(O)Cn2cnnc2O)C1 | unichem_smiles | 29 |
COc1ccc(-c2cc(C(=O)N/N=C\c3ccc(Br)cc3)n[nH]2)c(OC)c1 | unichem_smiles | 42 |
C[C@H](Nc1ccc2c(c1)OCCO2)C(O)=NC(=N)O | unichem_smiles | 31 |
COc1ccc(CN(C(=O)CC(CN)OC)c2nccs2)c(OC)c1.Cl | unichem_smiles | 33 |
CCn1cc(S(=O)(=O)N2CC3(CCOCC3)C2C(C)C)nc1C | unichem_smiles | 34 |
COc1ccc(CCN2C(=O)c3cc4ccccc4n3C[C@]2(C)C(O)=NCCC(C)C)cc1OC | unichem_smiles | 45 |
C=Nc1c(-c2ccc(-c3ccccc3)nc2)cnn1/C(N)=C(\CC1CCC(CNC)N1C(=O)C(N)=NC=N)C(=C)C | unichem_smiles | 58 |
OC[C@@H]1[C@H](CO)ON(Cc2ccc(C#Cc3ccccc3)cc2)[C@@H]1C(O)=NCCc1c[nH]c2ccccc12 | unichem_smiles | 56 |
CCCC[C@H](C(=N)O)[C@@H](CC1CC1)C(O)=NC1N=C(c2ccccc2)c2ccccc2N(Cc2cccc(-c3ccc(OC)cc3)c2)C1=O | unichem_smiles | 66 |
COc1cc2c(cc1OC)[C@H]1CC(O)C(CC(C)C)CN1CC2 | unichem_smiles | 32 |
COc1ccc2oc(-c3ccc(C)c(N=C(O)C=Cc4ccc(-c5ccc(Cl)cc5)o4)c3)nc2c1 | unichem_smiles | 47 |
O=C1c2cccnc2C(=O)N1C1CCCC1CO | unichem_smiles | 21 |
CC(C)(CC1C=C(N2Cc3ccccc3C2)c2ccccc21)N=[N+]=[N-] | unichem_smiles | 36 |
CCc1[nH]c(=N)ccc1-c1ccccc1OC(F)(F)F | unichem_smiles | 27 |
COc1cc(NS(=O)(=O)c2ccc(N3CCCCC3=O)cc2)cc(OC)c1OC | unichem_smiles | 35 |
Cc1nc(C)n(-c2ccccc2N=C(O)CCCS(=O)(=O)N2CCCC2)n1 | unichem_smiles | 36 |
Cc1cc(N=C(O)c2nc(C(C)C)n(-c3ccccc3Cl)n2)ccc1C(N)=O | unichem_smiles | 40 |
Cc1ccc(OCC(O)=NN=C(O)Cc2ccc(Br)cc2)cc1C | unichem_smiles | 29 |
CC(C)N1C2CCC1CN(C(=O)[C@@H]1CCO[C@H]1c1ccnn1C)CC2 | unichem_smiles | 39 |
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