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UMB-32

CAS No.
1635437-39-6
Chemical Name:
UMB-32
Synonyms
UMB-32;Imidazo[1,2-a]pyrazin-3-amine, N-(1,1-dimethylethyl)-2-[4-(3,5-dimethyl-4-isoxazolyl)phenyl]-
CBNumber:
CB63152757
Molecular Formula:
C21H23N5O
Molecular Weight:
361.44
MDL Number:
MFCD32645114
MOL File:
1635437-39-6.mol
Last updated:2023-05-21 10:59:17

UMB-32 Properties

Density 1.23±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility ≤20mg/ml in ethanol;10mg/ml in DMSO;20mg/ml in dimethyl formamide
form crystalline solid
pka 4.30±0.30(Predicted)

UMB-32 price More Price(11)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 17123 UMB-32 ≥98% 1635437-39-6 1mg $49 2024-03-01 Buy
Cayman Chemical 17123 UMB-32 ≥98% 1635437-39-6 5mg $216 2024-03-01 Buy
Cayman Chemical 17123 UMB-32 ≥98% 1635437-39-6 10mg $380 2024-03-01 Buy
Cayman Chemical 17123 UMB-32 ≥98% 1635437-39-6 25mg $830 2024-03-01 Buy
TRC U700940 UMB-32 1635437-39-6 1mg $50 2021-12-16 Buy
Product number Packaging Price Buy
17123 1mg $49 Buy
17123 5mg $216 Buy
17123 10mg $380 Buy
17123 25mg $830 Buy
U700940 1mg $50 Buy

UMB-32 Chemical Properties,Uses,Production

Uses

UMB-32 is a novel and potent BET bromodomain (BRD4) inhibitor.

Biological Activity

umb-32 is a potent, selective inhibitor of the bet bromodomain brd4 [1]. the bet family (brd2, brd3, brd4, and brdt) functions as transcriptional coactivator proteins. bet bromodomains are also important mediators of cell cycle progression and facilitate developmental transitions such as spermiogenesis. deregulation of bet bromodomain function has been observed in numerous malignancies. bet bromodomain inhibition has contributed new insights into gene regulation and emerged as a promising therapeutic strategy in cancer [1].

in vitro

umb-32 bound to brd4 with a kd value of 550 nm and 724 nm cellular potency in brd4-dependent lines. umb-32 showed potency against taf1, a bromodomain-containing transcription factor. umb-32 showed markedly increased potency for the bet proteins associated with a dramatic improvement in selectivity. umb-32 potently bound to the taf1 and taf1l with the kd values of 560nm and 1.3 μm, respectively [1].

References

[1] mckeown m r, shaw d l, fu h, et al. biased multicomponent reactions to develop novel bromodomain inhibitors[j]. journal of medicinal chemistry, 2014, 57(21): 9019-9027.

UMB-32 Preparation Products And Raw materials

Raw materials

Preparation Products

UMB-32 Suppliers

Global( 16)Suppliers
Supplier Tel Email Country ProdList Advantage
BOC Sciences 16314854226 info@bocsci.com United States 9923 65
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 sales@chemegen.com China 11217 58
MedBioPharmaceutical Technology Inc 021-69568360 18916172912 order@med-bio.cn China 8140 58
TargetMol Chemicals Inc. 4008200310 marketing@tsbiochem.com China 24649 58
Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 11974 58
ApexBio Technology -- sales@apexbt.com United States 6251 58
UMB-32 Imidazo[1,2-a]pyrazin-3-amine, N-(1,1-dimethylethyl)-2-[4-(3,5-dimethyl-4-isoxazolyl)phenyl]- 1635437-39-6