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Details

Stereochemistry ACHIRAL
Molecular Formula C23H24N4O3S
Molecular Weight 436.527
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METESIND

SMILES

CN(CC1=CC=C(C=C1)S(=O)(=O)N2CCOCC2)C3=CC=C4N=C(N)C5=CC=CC3=C45

InChI

InChIKey=CVEGTZWWWRJCFK-UHFFFAOYSA-N
InChI=1S/C23H24N4O3S/c1-26(21-10-9-20-22-18(21)3-2-4-19(22)23(24)25-20)15-16-5-7-17(8-6-16)31(28,29)27-11-13-30-14-12-27/h2-10H,11-15H2,1H3,(H2,24,25)

HIDE SMILES / InChI

Molecular Formula C23H24N4O3S
Molecular Weight 436.527
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Metesind (AG-331) is a lipophilic thymidylate synthase inhibitor. It inhibits the cofactor binding site of the enzyme. It exerts cytotoxic properties. Metesind was being developed as an anticancer and antimetabolite agent.

Approval Year

PubMed

PubMed

TitleDatePubMed
Biological activity of a novel rationally designed lipophilic thymidylate synthase inhibitor.
1994
Product development of AG-331 lyophilized powder for injection.
1994 Jan-Feb
Contrasting patterns of DNA fragmentation induced by thymidylate synthase inhibitors, ZD1694 and AG-331.
1995

Sample Use Guides

In Vitro Use Guide
H35 cells treated with 10 microM AG-331 were shown to accumulate in the S phase of the cell cycle. However, when treatments were conducted at a 5-fold higher concentration of AG-331, no S-phase block was apparent, suggesting the loss of a TS-directed effect at high inhibitor concentrations.
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:11:20 UTC 2023
Edited
by admin
on Sat Dec 16 17:11:20 UTC 2023
Record UNII
2027T69J24
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METESIND
INN  
Official Name English
metesind [INN]
Common Name English
Metesind [WHO-DD]
Common Name English
4-((4-(((2-AMINOBENZ(CD)INDOL-6-YL)METHYLAMINO)METHYL)PHENYL)SULFONYL)MORPHOLINE
Systematic Name English
Code System Code Type Description
SMS_ID
100000081204
Created by admin on Sat Dec 16 17:11:20 UTC 2023 , Edited by admin on Sat Dec 16 17:11:20 UTC 2023
PRIMARY
FDA UNII
2027T69J24
Created by admin on Sat Dec 16 17:11:20 UTC 2023 , Edited by admin on Sat Dec 16 17:11:20 UTC 2023
PRIMARY
EPA CompTox
DTXSID90930100
Created by admin on Sat Dec 16 17:11:20 UTC 2023 , Edited by admin on Sat Dec 16 17:11:20 UTC 2023
PRIMARY
INN
7493
Created by admin on Sat Dec 16 17:11:20 UTC 2023 , Edited by admin on Sat Dec 16 17:11:20 UTC 2023
PRIMARY
ChEMBL
CHEMBL9440
Created by admin on Sat Dec 16 17:11:20 UTC 2023 , Edited by admin on Sat Dec 16 17:11:20 UTC 2023
PRIMARY
PUBCHEM
3047716
Created by admin on Sat Dec 16 17:11:20 UTC 2023 , Edited by admin on Sat Dec 16 17:11:20 UTC 2023
PRIMARY
NCI_THESAURUS
C166526
Created by admin on Sat Dec 16 17:11:20 UTC 2023 , Edited by admin on Sat Dec 16 17:11:20 UTC 2023
PRIMARY
CAS
138384-68-6
Created by admin on Sat Dec 16 17:11:20 UTC 2023 , Edited by admin on Sat Dec 16 17:11:20 UTC 2023
PRIMARY
EVMPD
SUB08828MIG
Created by admin on Sat Dec 16 17:11:20 UTC 2023 , Edited by admin on Sat Dec 16 17:11:20 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY