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Merck
모든 사진(1)

주요 문서

SML1327

Sigma-Aldrich

Glutaminase Inhibitor 968

≥98% (HPLC)

동의어(들):

5-(3-Bromo-4-(dimethylamino)phenyl)-2,2-dimethyl-2,3,5,6-tetrahydrobenzo[a]phenanthridin-4(1H)-one

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About This Item

실험식(Hill 표기법):
C27H27BrN2O
CAS Number:
Molecular Weight:
475.42
UNSPSC 코드:
12352200
NACRES:
NA.77

Quality Level

분석

≥98% (HPLC)

양식

powder

색상

white to beige

solubility

DMSO: 5 mg/mL, clear (warmed)

저장 온도

2-8°C

SMILES string

Brc1c(ccc(c1)C2Nc3c(c5c(cc3)cccc5)C4=C2C(=O)CC(C4)(C)C)N(C)C

InChI

1S/C27H27BrN2O/c1-27(2)14-19-24-18-8-6-5-7-16(18)9-11-21(24)29-26(25(19)23(31)15-27)17-10-12-22(30(3)4)20(28)13-17/h5-13,26,29H,14-15H2,1-4H3

InChI key

NVFRRJQWRZFDLM-UHFFFAOYSA-N

일반 설명

Glutaminase Inhibitor 968 belongs to the benzophenanthridinone family.

애플리케이션

Glutaminase inhibitor 968 has been used to study the role of glutamine metabolism in macrophage activation.

생화학적/생리학적 작용

Glutaminase Inhibitor 968 is an allosteric inihibitor of the mitochondrial enzyme glutaminase C (GAC), which is overexpressed in a number of cancer cell lines. Glutaminase Inhibitor 968 shows 21% inhibition at 10 μM, 94% at 25 μM. Glutaminase Inhibitor 968 blocked human cancer cell proliferation in culture, and in inhibited tumor formation in mouse xenograft models.
Glutaminase Inhibitor 968 is an allosteric inihibitor of the mitochondrial enzyme glutaminase C (GAC).
Variation in the 3-bromo-4-(dimethylamino)phenyl ring of glutaminase inhibitor 968, leads to loss of its inhibitory activity. Glutaminase catalysed glutamine metabolism maintains intracellular pH of cancer cells. Inhibition by glutaminase inhibitor 968 is known to hinder cell proliferation as a consequences of low intracellular pH.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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문서 라이브러리 방문

Dibenzophenanthridines as Inhibitors of Glutaminase C and Cancer Cell Proliferation
Katt W P, et al.
Molecular Cancer Therapeutics, 11(6) (2012)
Glutaminase: a hot spot for regulation of cancer cell metabolism?.
Erickson J W and Cerione R A
Oncotarget, 1(8), 734-734 (2010)
α-ketoglutarate orchestrates macrophage activation through metabolic and epigenetic reprogramming.
Liu P S, et al.
Nature Immunology, 18(9), 985-985 (2017)
Glutaminase regulation in cancer cells: a druggable chain of events.
Katt W P and Cerione R A
Drug Discovery Today, 19(4), 450-457 (2014)
Shuting Han et al.
Theranostics, 11(17), 8464-8479 (2021-08-11)
As glutamine plays a central role in cancer metabolism, inhibition of glutaminolysis has become an ideal anticancer therapeutic target. However, glutaminolysis inhibition leads to activation of autophagy, which compromises its antitumor effect. Hence, we investigated the mechanism underlying glutaminolysis inhibition-induced

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