Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D0R3XO
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| Former ID |
DNC008033
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| Drug Name |
Cyclo(-L-Am7(S2Py)-Aib-L-Ala-D-Pro-)
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| Synonyms |
CHEMBL238596; cyclo(-L-Am7(S2Py)-Aib-L-Ala-D-Pro-); BDBM50222727
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
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Download2D MOL |
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| Formula |
C24H35N5O4S2
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| Canonical SMILES |
CC1C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)N1)(C)C)CCCCCSSC3=CC=CC=N3
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| InChI |
1S/C24H35N5O4S2/c1-16-22(32)29-14-9-11-18(29)21(31)27-17(20(30)28-24(2,3)23(33)26-16)10-5-4-8-15-34-35-19-12-6-7-13-25-19/h6-7,12-13,16-18H,4-5,8-11,14-15H2,1-3H3,(H,26,33)(H,27,31)(H,28,30)/t16-,17-,18+/m0/s1
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| InChIKey |
SNOZDSAKXKVXTD-OKZBNKHCSA-N
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| PubChem Compound ID | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Molecular design of histone deacetylase inhibitors by aromatic ring shifting in chlamydocin framework. Bioorg Med Chem. 2007 Dec 15;15(24):7830-9. | |||
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