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OU749

CAS No.
519170-13-9
Chemical Name:
OU749
Synonyms
OU749;N-[5-(4-Methoxybenzyl)-1,3,4-thiadiazol-2-yl]benzenesulfonamide;Benzenesulfonamide, N-[5-[(4-methoxyphenyl)methyl]-1,3,4-thiadiazol-2-yl]-
CBNumber:
CB52591897
Molecular Formula:
C16H15N3O3S2
Molecular Weight:
361.44
MDL Number:
MFCD03351667
MOL File:
519170-13-9.mol
Last updated:2023-07-16 08:27:58

OU749 Properties

storage temp. 2-8°C
solubility DMSO: >20mg/mL
form solid
color white to off-white

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P330-P501
Hazard Codes  Xn
Risk Statements  22
NFPA 704
0
2 0

OU749 price More Price(8)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 13804 OU749 ≥95% 519170-13-9 1mg $23 2024-03-01 Buy
Cayman Chemical 13804 OU749 ≥95% 519170-13-9 5mg $100 2024-03-01 Buy
Cayman Chemical 13804 OU749 ≥95% 519170-13-9 10mg $177 2024-03-01 Buy
Cayman Chemical 13804 OU749 ≥95% 519170-13-9 25mg $384 2024-03-01 Buy
ApexBio Technology C4135 OU749 519170-13-9 25mg $437 2021-12-16 Buy
Product number Packaging Price Buy
13804 1mg $23 Buy
13804 5mg $100 Buy
13804 10mg $177 Buy
13804 25mg $384 Buy
C4135 25mg $437 Buy

OU749 Chemical Properties,Uses,Production

Biological Activity

ou749 is a competitive inhibitor of γ-glutamyl transpeptidase (ggt) [1].expression of γ-glutamyl transpeptidase (ggt) in tumors contributes to the resistance to radiation and chemotherapy. ggt is inhibited by glutamine analogues which compete with the substrate for the γ-glutamyl binding site [1].ou749 inhibited human kidney ggt with an intrinsic ki of 17.6 m [1]. in 786-o cells, a human renal tumor cell line, ou749 showed more than 150-fold less toxic than the ggt inhibitor acivicin toward dividing cells. ou749 inhibited ggt isolated from human kidney in a dose-dependent manner [1]. ou749 was 7-fold less potent as inhibitor of ggt isolated from rat kidney and 10-fold less potent inhibiting ggt from mouse kidney [1]. ou749 did not inhibit degradation of glutathione by ggt from rat kidney. inhibition of ggt by ou749 is species-specific [1]. ou749 showed no inhibitory effect on ggt from pig cells. ou749 inhibited human ggt expressed in mouse fibroblasts by a similar extent to the ggt from human cells, indicated that the species specificity was determined by differences in the primary structure of the protein rather than species-specific, post-translational modifications [1].

References

[1] king j b, west m b, cook p f, et al. a novel, species-specific class of uncompetitive inhibitors of γ-glutamyl transpeptidase[j]. journal of biological chemistry, 2009, 284(14): 9059-9065.

98-09-9
63617-18-5
519170-13-9
Synthesis of OU749 from Benzenesulfonyl chloride and 5-(4-METHOXY-BENZYL)-[1,3,4]THIADIAZOL-2-YLAMINE

OU749 Preparation Products And Raw materials

Raw materials

Preparation Products

OU749 Suppliers

Global( 28)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
MedBioPharmaceutical Technology Inc 021-69568360 18916172912 order@med-bio.cn China 8141 58
TargetMol Chemicals Inc. 4008200310 marketing@tsbiochem.com China 24131 58
Suzhou Zhixin Biotechnology Co., Ltd. 0512-65118909 15162312715 sales@szzxbio.com China 2999 58
Nanjing Tengyi Biotechnology Co., Ltd 025-58851786 17714337195 sales@tybiochem.com China 4257 58
Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 8740 58
ApexBio Technology -- sales@apexbt.com United States 6254 58
Nanjing Shizhou Biology Technology Co.,Ltd 025-85560043 15850508050 cindy.huang@synzest.com China 12007 58
N-[5-(4-Methoxybenzyl)-1,3,4-thiadiazol-2-yl]benzenesulfonamide OU749 Benzenesulfonamide, N-[5-[(4-methoxyphenyl)methyl]-1,3,4-thiadiazol-2-yl]- 519170-13-9