ChemicalBook--->CAS DataBase List--->869296-13-9

869296-13-9

869296-13-9 Structure

869296-13-9 Structure
IdentificationBack Directory
[Name]

T-26c
[CAS]

869296-13-9
[Synonyms]

T-26c
CPD1612
T-26c >=98% (HPLC)
Benzoic acid, 4-[[[1,4-dihydro-2-[[[(3-methoxyphenyl)methyl]amino]carbonyl]-4-oxothieno[2,3-d]pyrimidin-5-yl]methoxy]methyl]-
[Molecular Formula]

C24H21N3O6S
[MDL Number]

MFCD31558511
[MOL File]

869296-13-9.mol
[Molecular Weight]

479.51
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 10 mg/ml
[form ]

A crystalline solid
[color ]

White to off-white
[InChIKey]

CDQRIIUMNLMHRH-UHFFFAOYSA-N
[SMILES]

C(O)(=O)C1=CC=C(COCC2C3C(=O)N=C(C(NCC4=CC=CC(OC)=C4)=O)NC=3SC=2)C=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

T-26c is highly potent and selective matrix metalloproteinase-13 (MMP-13) inhibitor with an IC50 of 6.75 pM and more than 2600-fold selectivity over the other related metalloenzymes[1].
[Biological Activity]

T-26c is a highly potentselective and cell-permeable matrix metalloproteinases 13 (MMP-13) inhibitor. T-26c inhibits the breakdown of collagen (87.4% inhibition at 0.1 μM) in IL-1b and oncostatin M stimulated cartilage. For full characterization detailsplease visit the T-26c probe summary on the Structural Genomics Consortium (SGC) website.

To learn about other SGC chemical probes for protein targetsvisit sigma.com/sgc
[in vivo]

T-26c is well absorbed in all species at the oral dose of 10–20 mg/kg. Oral administration of the disodium salt formulations of T-26c to guinea pigs results in significant increases in AUC (8357 ng h/mL) and Cmax (1445 ng/ mL) compared with those of the free acid T-26c (AUC = 6478 ng h/ mL and Cmax= 911 ng/mL)[1].

[References]

[1] Nara H, et al. Thieno[2,3-d]pyrimidine-2-carboxamides bearing a carboxybenzene group at 5-position: highly potent, selective, and orally available MMP-13 inhibitors interacting with the S1″ binding site. Bioorg Med Chem. 2014 Oct 1;22(19):5487-505. DOI:10.1016/j.bmc.2014.07.025
Spectrum DetailBack Directory
[Spectrum Detail]

T-26c(869296-13-9)1HNMR
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