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ARQ 621
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
ARQ 621图片
CAS NO:1095253-39-6
规格:≥98%
包装与价格:
包装价格(元)
2mg询价
5mg询价
10mg询价
25mg询价
50mg询价
100mg询价
250mg询价

理化性质和储存条件
Molecular Weight (MW)552.43
FormulaC28H24Cl2FN5O2
CAS No.1095253-39-6
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 100 mg/mL (181.0 mM)
Water:<1 mg/mL
Ethanol: 100 mg/mL (181.0 mM)
Other info

Chemical Name: (R)-N-(3-aminopropyl)-3-chloro-N-(1-(7-chloro-4-oxo-3-(phenylamino)-3,4-dihydroquinazolin-2-yl)but-3-yn-1-yl)-2-fluorobenzamide

InChi Key: UPJSUQWHUVLLNW-XMMPIXPASA-N

InChi Code: InChI=1S/C28H24Cl2FN5O2/c1-2-8-24(35(16-7-15-32)27(37)21-11-6-12-22(30)25(21)31)26-33-23-17-18(29)13-14-20(23)28(38)36(26)34-19-9-4-3-5-10-19/h1,3-6,9-14,17,24,34H,7-8,15-16,32H2/t24-/m1/s1

SMILES Code: O=C(N(CCCN)[C@@H](C(N1NC2=CC=CC=C2)=NC3=C(C=CC(Cl)=C3)C1=O)CC#C)C4=CC=CC(Cl)=C4F

SynonymsARQ621; ARQ 621; ARQ-621
实验参考方法
In Vitro

In vitro activity: ARQ 621 demonstrates anti-tumor activity against a wide range of human cancer cell lines in vitro, including colon, lung, endometrial, bladder, and hematologic cancer cell lines, with significantly less cytotoxicity against hematopoietic cells.

In VivoARQ 621, as a novel clinical stage drug candidate, inhibits a number of xenografts grown in athymic mice, such as pancreatic, breast, prostate, and ovarian carcinomas with no hematological changes. Furthermore, for ARQ 621, there is no envidence of bone marrow toxicity in pre-clinical mouse efficacy models or safety studies in rats and dogs.
Animal model
Formulation & Dosage
References

Rosen L, et al. Annual Meeting of ASCO: abstract 3076.

 
 
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