U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C62H111N11O13
Molecular Weight 1218.6106
Optical Activity UNSPECIFIED
Defined Stereocenters 13 / 13
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CYCLOSPORIN C

SMILES

[H][C@]1(NC(=O)[C@]([H])([C@H](O)[C@H](C)C\C=C\C)N(C)C(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](NC(=O)[C@H](CC(C)C)N(C)C(=O)CN(C)C1=O)C(C)C)[C@@H](C)O

InChI

InChIKey=JTOKYIBTLUQVQV-QRVTZXGZSA-N
InChI=1S/C62H111N11O13/c1-25-26-27-39(14)52(76)51-56(80)66-49(42(17)74)60(84)67(18)32-47(75)68(19)43(28-33(2)3)55(79)65-48(37(10)11)61(85)69(20)44(29-34(4)5)54(78)63-40(15)53(77)64-41(16)57(81)70(21)45(30-35(6)7)58(82)71(22)46(31-36(8)9)59(83)72(23)50(38(12)13)62(86)73(51)24/h25-26,33-46,48-52,74,76H,27-32H2,1-24H3,(H,63,78)(H,64,77)(H,65,79)(H,66,80)/b26-25+/t39-,40+,41-,42-,43+,44+,45+,46+,48+,49+,50+,51+,52-/m1/s1

HIDE SMILES / InChI

Approval Year

Targets
PubMed

PubMed

TitleDatePubMed
Mode of action of SDZ NIM 811, a nonimmunosuppressive cyclosporin A analog with activity against human immunodeficiency virus (HIV) type 1: interference with HIV protein-cyclophilin A interactions.
1995 Apr
Inhibition of vaccinia virus replication by cyclosporin A analogues correlates with their affinity for cellular cyclophilins.
1998 Feb
Name Type Language
CYCLOSPORIN C
MI  
Common Name English
CYCLOSPORIN A, 7-L-THREONINE-
Common Name English
THR2-CYCLOSPORINE
Common Name English
CYCLO(L-ALANYL-D-ALANYL-N-METHYL-L-LEUCYL-N-METHYL-L-LEUCYL-N-METHYL-L-VALYL-(3R,4R,6E)-6,7-DIDEHYDRO-3-HYDROXY-N,4-DIMETHYL-L-2-AMINOOCTANOYL-L-THREONYL-N-METHYLGLYCYL-N-METHYL-L-LEUCYL-L-VALYL-N-METHYL-L-LEUCYL)
Common Name English
CYCLOSPORIN C [MI]
Common Name English
Code System Code Type Description
MERCK INDEX
m4020
Created by admin on Sat Dec 16 08:18:19 GMT 2023 , Edited by admin on Sat Dec 16 08:18:19 GMT 2023
PRIMARY Merck Index
CAS
59787-61-0
Created by admin on Sat Dec 16 08:18:19 GMT 2023 , Edited by admin on Sat Dec 16 08:18:19 GMT 2023
PRIMARY
PUBCHEM
5287817
Created by admin on Sat Dec 16 08:18:19 GMT 2023 , Edited by admin on Sat Dec 16 08:18:19 GMT 2023
PRIMARY
FDA UNII
6S744L5508
Created by admin on Sat Dec 16 08:18:19 GMT 2023 , Edited by admin on Sat Dec 16 08:18:19 GMT 2023
PRIMARY
EPA CompTox
DTXSID501017530
Created by admin on Sat Dec 16 08:18:19 GMT 2023 , Edited by admin on Sat Dec 16 08:18:19 GMT 2023
PRIMARY