Compound Search
化合物数据库
基于 PubChem CID 索引，支持名称 / 同义词 / CAS / SMILES 检索。
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Step 1. Synthesis of Intermediate 9-1 PubChem CID 172430216
CC(C)C(O)c1cccc([C@H](C)NC2NC(=O)N(C3CCOCC3)C(=O)N2)c1 -
Example 524 (Iron Metal as Reducing Agent for Step 2) PubChem CID 172879082
CC1(O)CCN(c2cccc3c2ccn3-c2ccc3ncnc(Nc4c(F)ccc(NS(=O)(=O)c5cccc(Cl)c5Cl)c4F)c3n2)CC1 -
Example 524 (Iron Metal as Reducing Agent for Step 2) PubChem CID 172879098
CC(C)C1(O)CCN(c2cccc3c2ccn3-c2ccc3ncnc(Nc4c(F)ccc(NS(=O)(=O)c5cccc(Cl)c5Cl)c4F)c3n2)CC1 -
Step 1: Di-tert-butyl (3,5-difluoro-3''-(methoxy-d3)-[1,1''-biphenyl]-4-yl)iminodicarbonate (13a) PubChem CID 176456093
[2H]C([2H])([2H])Oc1cccc(-c2cc(F)c(CN(C)C(=O)C3=C(C(=O)NOC)CCC3)c(F)c2)c1 -
Step 1: Preparation of (Z)-2-cyano-3-(dimethylamino)acryloyl chloride and 2-cyanoacetyl chloride PubChem CID 176799640
CN(C)/C=C(/C#N)C(=O)N1CCC(Nc2cc(C(=O)N3CC[C@H](N4CCc5ccccc5C4)[C@@H](O)C3)ncn2)CC1 -
Step 8: (R)-N-((S)-1-(7-ethyl-6-oxo-5,6-dihydro-1,5-naphthyridin-3-yl)ethyl)-2-methylpropane-2-sulfinamide PubChem CID 176886667
CCc1cc2ncc([C@H](C)N3CC(Oc4ccc(C(=O)NC)nc4)C3)cc2[nH]c1=O -
O=C(O)c1ccccc1O -
C#C[C@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@@]21CC -
CCCCCCCCCCC(C(=O)OC)S(=O)(=O)[O-].[Na+] -
CC(C)O.NC(=NCCCCCCN=C(N)/N=C(\N)Nc1ccc(Cl)cc1)/N=C(\N)Nc1ccc(Cl)cc1.O=C(O)C[C@@H](O)[C@H](O)[C@H](O)CO.O=C(O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO -
Essentials Scalp Control Deep Clean with Invigorating Mint Anti-Dandruff Shampoo CAS 13463-41-7 PubChem CID 26041
[O-][n+]1ccccc1[S-].[O-][n+]1ccccc1[S-].[Zn+2] -
3,3 OE,5,5 OE-Tetramethylbenzidine pound>>BM blue; Sure Blue TMB; TMB Blotting Plus; TMB substrate pound>>TMB CAS 54827-17-7 PubChem CID 41206
Cc1cc(-c2cc(C)c(N)c(C)c2)cc(C)c1N -
(3S)-3-[[5-[2-morpholin-4-yl-4-(trifluoromethyl)phenyl]-1,3,4-oxadiazol-2-yl]amino]-5-phenyl-1,3-dihydro-1,4-benzodiazepin-2-one PubChem CID 134461121
O=C1Nc2ccccc2C(c2ccccc2)=N[C@@H]1Nc1nnc(-c2ccc(C(F)(F)F)cc2N2CCOCC2)o1 -
US11390631, Example 148 PubChem CID 134461122
O=C1Nc2ccccc2C(c2ccccc2)=NC1Nc1nnc(-c2cccc(F)c2N2CCOCC2)o1 -
US11390631, Example 164 PubChem CID 134461151
Cn1cc(N2CCOCC2)c(-c2nnc(N[C@H]3N=C(c4ccccc4)c4ccccc4NC3=O)o2)n1 -
US11390631, Example 179 PubChem CID 134461164
O=C1Nc2ccccc2C(c2ccccc2)=N[C@@H]1Nc1nnc(-c2oc3ccccc3c2N2CCOCC2)o1 -
US11390631, Example 133 PubChem CID 134461196
O=C1Nc2ccccc2C(c2ccccc2)=NC1Nc1nnc(-c2cnccc2N2CCOCC2)o1 -
US11390631, Example 312 PubChem CID 134461236
O=C1Nc2ccccc2C(c2ccccc2)=N[C@@H]1Nc1nnc(-c2ncc(C3=CCCCC3)cc2N2CCOCC2)o1 -
US11390631, Example 135 PubChem CID 134461256
O=C1Nc2ccccc2C(c2ccccc2)=NC1Nc1nnc(-c2ncc(N3CCOCC3)cc2Cl)o1 -
US11390631, Example 324 PubChem CID 134461263
N#Cc1ccc(N2CCOCC2)c(-c2nnc(N[C@H]3N=C(c4ccccc4)c4ccccc4NC3=O)o2)n1