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Lomeguatrib

CAS No.
192441-08-0
Chemical Name:
Lomeguatrib
Synonyms
C521206;CS-1103;AI3 27596;BRN1861032;Lomeguatrib;Lomeguqtrib;BRN 1861032;BRN-1861032;Lomeguaritrib;Lomeguatrib, >=98%
CBNumber:
CB11261272
Molecular Formula:
C10H8BrN5OS
Molecular Weight:
326.17
MDL Number:
MFCD23703756
MOL File:
192441-08-0.mol
MSDS File:
SDS
Last updated:2023-06-30 15:45:59

Lomeguatrib Properties

Boiling point 683.8±65.0 °C(Predicted)
Density 2.07
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility DMSO: soluble10mg/mL, clear
pka 9.42±0.10(Predicted)
form powder
color white to beige
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 3 months.
FDA UNII S79265T71M

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338
Hazard Codes  Xn
Risk Statements  22
WGK Germany  3
RTECS  UO7420000
NFPA 704
0
2 0

Lomeguatrib price More Price(32)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML0586 Lomeguatrib ≥98% (HPLC) 192441-08-0 5mg $128 2024-03-01 Buy
Sigma-Aldrich SML0586 Lomeguatrib ≥98% (HPLC) 192441-08-0 25mg $397 2024-03-01 Buy
Cayman Chemical 11732 Lomeguatrib ≥98% 192441-08-0 5mg $38 2024-03-01 Buy
Cayman Chemical 11732 Lomeguatrib ≥98% 192441-08-0 10mg $67 2024-03-01 Buy
Cayman Chemical 11732 Lomeguatrib ≥98% 192441-08-0 25mg $146 2024-03-01 Buy
Product number Packaging Price Buy
SML0586 5mg $128 Buy
SML0586 25mg $397 Buy
11732 5mg $38 Buy
11732 10mg $67 Buy
11732 25mg $146 Buy

Lomeguatrib Chemical Properties,Uses,Production

Description

Lomeguatrib (192441-08-0) is a potent (IC50?= 9 nM) inhibitor of O6-Methylguanine-DNA Methyltransferase (MGMT), an important DNA repair protein.1?It is currently being investigated in cancers that have acquired resistant to the chemotherapeutic temozolomide2-5, as well as other chemotherapeutics6,7.

Uses

O6-Methylguanine-DNA methyltransferase (MGMT) is a DNA repair protein which removes an alkyl group from the O6 position on guanine in an autoinactivating reaction. Although important in normal DNA repair, this reaction confers resistance to treatments that use O6-alkylating agents to produce cytotoxicity, e.g., in cancer. Lomeguatrib is a modified quanine base which acts as a pseudosubstrate inactivator of MGMT (IC50 = ~3 nM). A non-toxic compound, lomeguatrib completely inactivates MGMT in human prostate and colorectal tumors when given as a single 120 mg oral dose and in primary central nervous system cancers at 160 mg.

Uses

Lomeguatrib is an inhibitor of O6-methylguanine-DNA methyltransferase (MGMT). Lomeguatrib attenuates MGMT activity in vitro and in vivo. Lomeguatrib enhances the antitumor activity of temozolomide in both human melanoma and MCF-7 xenografts.

storage

+4°C

References

1) Reinhard?et al.?(2001),?Monosaccharide-Linked Inhibitors of O6-Methylguanine-DNA Methyltransferase (MGMT): Synthesis, Molecular Modeling, and Structure-Activity Relationships; J. Med. Chem.?44?4050 2) Barvaux?et al.?(2004),?Sensitization of a human ovarian cancer cell line to temozolomide by simultaneous attenuation of the Bcl-2 antiapoptotic protein and DNA repair by O6-alkylguanine-DNA alkyltransferase: Mol. Cancer Ther.?3?1215 3) Gumbrell?et al.?(2006),?Lomeguatrib, a potent inhibitor of O6-alkylguanine-DNA-alkyltransferase: phase I safety, pharmacodynamic, and pharmacokinetic trial and evaluation in combination with temozolomide in patients with advanced solid tumors: Clin. Cancer Res.?12?1577 4) Watson?et al.?(2009),?O(6)-methylguanine-DNA methyltransferase depletion and DNA damage in patients with melanoma treated with temozolomide alone or with lomeguatrib: Br. J. Cancer?100?1250 5) Taspinar?et al.?(2013),?Effect of lomeguatrib-temozolomide combination of MGMT promoter methylation and expression in primary glioblastoma tumor cells: Tumour Biol.?34?1935 6) Sabharwal?et al.?(2010),?A phase I trial of lomeguatrib and irinotecan in metastatic colorectal cancer: Cancer Chemother. Pharmacol.?66?829 7) Tawbi?et al.?(2011),?Inhibition of DNA repair with MGMT pseudosubstrates: phase I study of lomeguatrib in combination with dacarbazine in patients with advanced melanoma and other solid tumors: Br. J. Cancer?105?773

Lomeguatrib Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 125)Suppliers
Supplier Tel Email Country ProdList Advantage
Nanjing ChemLin Chemical Industry Co., Ltd.
025-83697070 product@chemlin.com.cn CHINA 3012 60
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
BOC Sciences
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CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49390 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Career Henan Chemica Co
+86-0371-86658258 15093356674; laboratory@coreychem.com China 30255 58
HANGZHOU CLAP TECHNOLOGY CO.,LTD
86-571-88216897,88216896 13588875226 sales@hzclap.com CHINA 6313 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29067 58
Hefei Hirisun Pharmatech Co., Ltd
+8615056975894 shawn@hirisunpharm.com CHINA 9923 58

Lomeguatrib Spectrum

Lomeguatrib 2-Amino-6-[(4-bromo-2-thienyl)methoxy]-9H-purine 6-[(4-bromothiophen-2-yl)methoxy]-7H-purin-2-amine 6-((4-Bromo-2-thienyl)methoxy)purin-2-amine C521206 2-AMino-6-(4-broMothiophen-2-ylMethoxy)-9H-purine 6-[(4-BroMo-2-thienyl)Methoxy] -1H-purin-2-aMine 6-[(4-BroMo-2-thienyl)Methoxy]-9H-purin-2-aMine LoMeguatrib(PaTrin-2) 2-Amino-6-[(4-bromo-2-thienyl)methoxy]-9H-purine Lomeguatrib(PaTrin-2) 2-Amino-6-[(4-bromo-2-thienyl)methoxy]-9H-purine Lomeguatrib Lomeguatrib 2-Amino-6-[(4-bromo-2-thienyl)methoxy]-9H-purine Lomeguqtrib Lomeguaritrib Lomeguatrib, >=98% CS-1103 PATRIN 2; PATRIN-2 9H-Purin-2-amine, 6-[(4-bromo-2-thienyl)methoxy]- Lomeguatrib USP/EP/BP 6-((4-Bromothiophen-2-yl)methoxy)-9H-purin-2-amine AI3 27596 BRN 1861032 BRN1861032 BRN-1861032 192441-08-0 C10H8BrN5OS Inhibitors Inhibitor of MGMT. Epigenetics