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Details

Stereochemistry ACHIRAL
Molecular Formula C15H13N5OS
Molecular Weight 311.362
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Thiazovivin

SMILES

O=C(NCC1=CC=CC=C1)C2=CSC(NC3=NC=NC=C3)=N2

InChI

InChIKey=DOBKQCZBPPCLEG-UHFFFAOYSA-N
InChI=1S/C15H13N5OS/c21-14(17-8-11-4-2-1-3-5-11)12-9-22-15(19-12)20-13-6-7-16-10-18-13/h1-7,9-10H,8H2,(H,17,21)(H,16,18,19,20)

HIDE SMILES / InChI

Molecular Formula C15H13N5OS
Molecular Weight 311.362
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/19838168 |https://www.ncbi.nlm.nih.gov/pubmed/27647250

Thiazovivin is a novel ROCK (Rho-associated kinase) inhibitor and Rho-ROCK axis regulates cell-ECM and cell-cell adhesion. Recently was shown, that thiazovivin was effective for protecting the morphology and function of human corneal endothelial cells (HCECs). An optimal improvement in the morphology, connection and function of HCECs was found when the primary HCECs were cultured with thiazovivin.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
A chemical platform for improved induction of human iPSCs.
2009 Nov
Revealing a core signaling regulatory mechanism for pluripotent stem cell survival and self-renewal by small molecules.
2010 May 4
Reprogramming of endometrial adult stromal cells in the presence of a ROCK inhibitor, thiazovivin, could obtain more efficient iPSCs.
2015 May
Thiazovivin, a Rho kinase inhibitor, improves stemness maintenance of embryo-derived stem-like cells under chemically defined culture conditions in cattle.
2015 Oct
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
Thiazovivin (2 μM) inhibits ROCK activity and protects human embryonic stem cells
Substance Class Chemical
Created
by admin
on Sat Dec 16 20:02:00 GMT 2023
Edited
by admin
on Sat Dec 16 20:02:00 GMT 2023
Record UNII
7268XHE3P7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Thiazovivin
Common Name English
N-Benzyl-2-(pyrimidin-4-ylamino)thiazole-4-carboxamide
Systematic Name English
N-(Phenylmethyl)-2-(4-pyrimidinylamino)-4-thiazolecarboxamide
Systematic Name English
4-Thiazolecarboxamide, N-(phenylmethyl)-2-(4-pyrimidinylamino)-
Systematic Name English
Code System Code Type Description
PUBCHEM
46209426
Created by admin on Sat Dec 16 20:02:00 GMT 2023 , Edited by admin on Sat Dec 16 20:02:00 GMT 2023
PRIMARY
CAS
1226056-71-8
Created by admin on Sat Dec 16 20:02:00 GMT 2023 , Edited by admin on Sat Dec 16 20:02:00 GMT 2023
PRIMARY
FDA UNII
7268XHE3P7
Created by admin on Sat Dec 16 20:02:00 GMT 2023 , Edited by admin on Sat Dec 16 20:02:00 GMT 2023
PRIMARY