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You are searching for "CFAMM00320701" in compound.
Total 1 results found.
Click on CFAM IDs and names to search or view in CFAM, click on external IDs to view the entity in its source database.
| CFAM Mol ID | CFAMM00320701 |
| Family | CFFBM1217 Pol polyprotein inhibitor (2S)-4-benzyl-1-[(2S,4R)-4-benzyl-2-hydroxy-5-[[(2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]amino]-5-oxopentyl]-N-tert-butylpiperazine-2-carboxamide family |
| Superfamily | CFSBM696 Pol polyprotein Binder Superfamily 8 |
| Class | CFCBM26 Class 3076 |
| External ID | CHEMBL2062139 |
External Source | CHEMBL |
| PubChem CID |
5479520 |
Functional Category |
Bioactive |
| Molecule Name |
benzyl (3S)-4-[(2S,4R)-4-benzyl-2-hydroxy-5-[[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]amino]-5-oxopentyl]-3-(tert-butylcarbamoyl)piperazine-1-carboxylate |
| IUPAC Name |
benzyl (3S)-4-[(2S,4R)-4-benzyl-2-hydroxy-5-[[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]amino]-5-oxopentyl]-3-(tert-butylcarbamoyl)piperazine-1-carboxylate |
| Synonyms |
AC1L9U3L;L-732747;L-732,747;5-[2(S)-[(1,1-Dimethylethyl)aminocarbonyl]-4-[(phenylmethoxy)carbonyl]-1-piperazinyl]-4(S)-hydroxy-N-(2(R)-hydroxy-1(S)-indanyl)-2(R)-(phenylmethyl)pentanamide;benzyl (3S)-4-[(2S,4S)-4-benzyl-2-hydroxy-5-[[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]amino]-5-oxopentyl]-3-(tert-butylcarbamoyl)piperazine-1-carboxylate |
| InChi |
InChI=1S/C38H48N4O6/c1-38(2,3)40-36(46)32-24-42(37(47)48-25-27-14-8-5-9-15-27)19-18-41(32)23-30(43)21-29(20-26-12-6-4-7-13-26)35(45)39-34-31-17-11-10-16-28(31)22-33(34)44/h4-17,29-30,32-34,43-44H,18-25H2,1-3H3,(H,39,45)(H,40,46)/t29-,30+,32+,33-,34+/m1/s1 |
| InChiKey |
HOJASIJITQDJDA-PPJSLLJVSA-N |
| Formula | C38H48N4O6 |
Molecular Weight | 656.81 |
| Cross Link | CHEMBL2062139 |
| Structure |
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Statistics of CFAM Database |
CFAM currently contains 490,279 molecules in 87,136 families, 34,880 superfamilies and 11,643 classes.
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How to cite our database |
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C. Zhang, L. Tao, C. Qin, P. Zhang, S.Y. Chen, X. Zeng, F. Xu, Z. Chen, S.Y. Yang and Y.Z. CFam: A Chemical Families Database Based on Iterative Selection of Functional Seeds and Seed-Directed Compound Clustering.
Nucl. Acids Res. 43 (D1): D558-D565 (2015) (First published online: November 20, 2014).
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Last update by |
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2014.08.29
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Deputy
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National University of Singapore, Singapore
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