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Details

Stereochemistry ABSOLUTE
Molecular Formula C26H28N6O5S.ClH
Molecular Weight 573.064
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VALECOBULIN HYDROCHLORIDE

SMILES

Cl.COC1=CC(=CC(OC)=C1OC)C(=O)C2=CC=C(C=C2N3C=NC=N3)C4=CSC(NC(=O)[C@@H](N)C(C)C)=N4

InChI

InChIKey=FIAUXCMEQTWLQZ-FTBISJDPSA-N
InChI=1S/C26H28N6O5S.ClH/c1-14(2)22(27)25(34)31-26-30-18(11-38-26)15-6-7-17(19(8-15)32-13-28-12-29-32)23(33)16-9-20(35-3)24(37-5)21(10-16)36-4;/h6-14,22H,27H2,1-5H3,(H,30,31,34);1H/t22-;/m0./s1

HIDE SMILES / InChI

Molecular Formula C26H28N6O5S
Molecular Weight 536.603
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

CKD-516 is a prodrug of the tubulin binding agent S516, with potential tubulin-inhibiting, vascular-disrupting, and antineoplastic activity. Upon administration, tubulin polymerization inhibitor CKD-516 is converted into its active metabolite S-516, which binds to tubulin and prevents its polymerization in tumor blood vessel endothelial cells and tumor cells. This blocks the formation of the mitotic spindle and leads to cell cycle arrest at the G2/M phase. As a result, this agent disrupts the tumor vasculature and tumor blood flow, deprives tumor cells of nutrients and induces tumor cell apoptosis. In addition, this agent has a direct cytotoxic effect on tumor cells by inhibiting tubulin polymerization. CKD-516 is developed by a Korean company Chong Kun Dang Pharmaceutical Corp. and is investigated in a phase 1/2a clinical trial for the treatment of colorectal cancer in combination with Irinotecan.

Approval Year

Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:29:56 GMT 2025
Edited
by admin
on Mon Mar 31 21:29:56 GMT 2025
Record UNII
2J9QE0TM5I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CKD-516
Preferred Name English
VALECOBULIN HYDROCHLORIDE
Common Name English
BUTANAMIDE, 2-AMINO-3-METHYL-N-(4-(3-(1H-1,2,4-TRIAZOL-1-YL)-4-(3,4,5-TRIMETHOXYBENZOYL)PHENYL)-2-THIAZOLYL)-, HYDROCHLORIDE (1:1), (2S)-
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID80154196
Created by admin on Mon Mar 31 21:29:56 GMT 2025 , Edited by admin on Mon Mar 31 21:29:56 GMT 2025
PRIMARY
PUBCHEM
46929961
Created by admin on Mon Mar 31 21:29:56 GMT 2025 , Edited by admin on Mon Mar 31 21:29:56 GMT 2025
PRIMARY
FDA UNII
2J9QE0TM5I
Created by admin on Mon Mar 31 21:29:56 GMT 2025 , Edited by admin on Mon Mar 31 21:29:56 GMT 2025
PRIMARY
CAS
1240321-53-2
Created by admin on Mon Mar 31 21:29:56 GMT 2025 , Edited by admin on Mon Mar 31 21:29:56 GMT 2025
PRIMARY
SMS_ID
100000183474
Created by admin on Mon Mar 31 21:29:56 GMT 2025 , Edited by admin on Mon Mar 31 21:29:56 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY