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Details

Stereochemistry ABSOLUTE
Molecular Formula C34H47N9O12S3
Molecular Weight 869.985
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MK-852

SMILES

CC(=O)N[C@H]1CSSC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CC2=CC=C(CN)C=C2)NC(=O)[C@H]3N(CSC3(C)C)C(=O)[C@H](CC(N)=O)NC1=O)C(O)=O

InChI

InChIKey=IHTQUFFCUYSOIH-SBTHHMAGSA-N
InChI=1S/C34H47N9O12S3/c1-16(44)38-22-13-57-58-14-23(33(54)55)42-29(50)20(10-26(47)48)39-25(46)12-37-28(49)19(8-17-4-6-18(11-35)7-5-17)40-31(52)27-34(2,3)56-15-43(27)32(53)21(9-24(36)45)41-30(22)51/h4-7,19-23,27H,8-15,35H2,1-3H3,(H2,36,45)(H,37,49)(H,38,44)(H,39,46)(H,40,52)(H,41,51)(H,42,50)(H,47,48)(H,54,55)/t19-,20-,21-,22-,23-,27+/m0/s1

HIDE SMILES / InChI

Molecular Formula C34H47N9O12S3
Molecular Weight 869.985
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 6 / 6
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 20:23:10 GMT 2025
Edited
by admin
on Wed Apr 02 20:23:10 GMT 2025
Record UNII
74L3W95S34
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MK-852
Code English
L-367073
Preferred Name English
L-Cysteine, N-acetyl-L-cysteinyl-L-asparaginyl-5,5-dimethyl-L-4-thiazolidinecarbonyl-4-(aminomethyl)-L-phenylalanylglycyl-L-?-aspartyl-, cyclic (1?7)-disulfide
Systematic Name English
Code System Code Type Description
FDA UNII
74L3W95S34
Created by admin on Wed Apr 02 20:23:10 GMT 2025 , Edited by admin on Wed Apr 02 20:23:10 GMT 2025
PRIMARY
PUBCHEM
101653436
Created by admin on Wed Apr 02 20:23:10 GMT 2025 , Edited by admin on Wed Apr 02 20:23:10 GMT 2025
PRIMARY
CAS
138199-64-1
Created by admin on Wed Apr 02 20:23:10 GMT 2025 , Edited by admin on Wed Apr 02 20:23:10 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY
At infusion rates of 1 ?g/kg/min for 1 hour and 0.44 ?g/kg/min for 4 hours, respectively, MK-852 extended baseline bleeding time by greater than 2.2-fold and 2.6-fold, inhibited ADP-induced platelet aggregation by 76% and 69%, and inhibited collagen-induced platelet aggregation by 65% and 67%, respectively.