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AMG 900

CAS No.
945595-80-2
Chemical Name:
AMG 900
Synonyms
AMG 900;AMG-900;AMG900;AMG 900 USP/EP/BP;N-(4-((3-(2-Aminopyrimidin-4-yl)pyridin-2-yl)oxy)phenyl)-4-(4-methylthiophen-2-yl)phthalazin-1;N-[4-[[3-(2-Amino-4-pyrimidinyl)-2-pyridinyl]oxy]phenyl]-4-(4-methyl-2-thienyl)-1-phthalazinamine;1-Phthalazinamine, N-[4-[[3-(2-amino-4-pyrimidinyl)-2-pyridinyl]oxy]phenyl]-4-(4-methyl-2-thienyl)-;N-[4-[[3-(2-Amino-4-pyrimidinyl)-2-pyridinyl]oxy]phenyl]-4-(4-methyl-2-thienyl)-1-phthalazinamine AMG 900
CBNumber:
CB82554079
Molecular Formula:
C28H21N7OS
Molecular Weight:
503.58
MDL Number:
MFCD18633194
MOL File:
945595-80-2.mol
Last updated:2023-05-18 11:31:10

AMG 900 Properties

Boiling point 778.7±70.0 °C(Predicted)
Density 1.380
storage temp. 2-8°C(protect from light)
solubility ≥25.2 mg/mL in DMSO; insoluble in H2O; insoluble in EtOH
form solid
pka 4.79±0.30(Predicted)
FDA UNII 9R2G075611

AMG 900 price More Price(36)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 19176 AMG 900 ≥98% 945595-80-2 1mg $44 2024-03-01 Buy
Cayman Chemical 19176 AMG 900 ≥98% 945595-80-2 5mg $193 2024-03-01 Buy
Cayman Chemical 19176 AMG 900 ≥98% 945595-80-2 10mg $347 2024-03-01 Buy
Cayman Chemical 19176 AMG 900 ≥98% 945595-80-2 25mg $778 2024-03-01 Buy
Biosynth Carbosynth FA43339 N-(4-(3-(2-Aminopyrimidin-4-yl)pyridin-2-yloxy)phenyl)-4-(4-methylthiophen-2-yl)phthalazin-1-amine 945595-80-2 25mg $875 2021-12-16 Buy
Product number Packaging Price Buy
19176 1mg $44 Buy
19176 5mg $193 Buy
19176 10mg $347 Buy
19176 25mg $778 Buy
FA43339 25mg $875 Buy

AMG 900 Chemical Properties,Uses,Production

Description

Three Aurora kinases, A-C, are involved in phosphorylation events that are critical for the completion of mitosis. Their expression is elevated in a variety of human cancers. AMG 900 is an orally bioavailable, selective Aurora kinase inhibitor with IC50 values of 5, 4, and 1 nM for Aurora A, B, and C, respectively. It is greater than 10-fold selective for Aurora kinases over p38α, TYK2, JNK2, Met, and Tie2 (IC50s = 53, 220, 520, 550, and 650 nM, respectively). At 2-3 nM, AMG 900 has been shown to inhibit the proliferation of 26 different tumor cell lines in vitro, including cell lines resistant to either the antimitotic agent paclitaxel or to other Aurora kinase inhibitors. Furthermore, AMG 900 is reported to be broadly active in multiple xenograft models, including three multidrug-resistant xenograft models, representing five tumor types.

Enzyme inhibitor

This potent and highly selective mitotic protein kinase inhibitor (FW = 503.58 g/mol; CAS 945595-80-2; Solubility: 100 mg/mL DMSO), also named N-(4-(3-(2-aminopyrimidin-4-yl)pyridin-2-yloxy)phenyl)-4-(4- methylthiophen-2-yl)phthalazin-1-amine, targets Aurora A (IC50 = 5 nM), Aurora B (IC50 = 4 nM), and Aurora C (IC50 = 1 nM) protein kinases, with >10-fold selectivity versus p38α, Tyk2, JNK2, Met and Tie2. The modal tumor cell response to AMG 900 treatment is aborted cell division without prolonged mitotic arrest, ultimately resulting in cell death. AMG 900 exhibits acceptable PK properties in preclinical species and is predicted to have low clearance in humans. Male rats metabolize AMG 900 primarily through hydroxylation with subsequent sulfate conjugation on the pyrimidinyl-pyridine side-chain, whereas female rats favor oxidation on the thiophene ring's methyl group, which is then metabolized to a carboxylic acid, attended by conjugation to an acyl glucuronide. At low-nM concentrations, AMG 900, whether administered alone or in combination with microtubule-targeting drugs (paclitaxel or ixabepilone), may be an effective intervention strategy for the treatment of metastatic breast cancer and provide potential therapeutic options for patients with multidrug-resistant tumors. It is, in fact, also active against taxaneresistant tumor cell lines.

target

Aurora A

References

1. payton, m., et al., preclinical evaluation of amg 900, a novel potent and highly selective pan-aurora kinase inhibitor with activity in taxane-resistant tumor cell lines. cancer res, 2010. 70(23): p. 9846-54.2. geuns-meyer, s., et al., discovery of n-(4-(3-(2-aminopyrimidin-4-yl)pyridin-2-yloxy)phenyl)-4- (4-methylthiophen-2-yl)p hthalazin-1-amine (amg 900), a highly selective, orally bioavailable inhibitor of aurora kinases with activity against multidrug-resistant cancer cell lines. j med chem, 2015. 58(13): p. 5189-207.

AMG 900 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 94)Suppliers
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ATK CHEMICAL COMPANY LIMITED
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CONIER CHEM AND PHARMA LIMITED
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Career Henan Chemica Co
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Zhejiang J&C Biological Technology Co.,Limited
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InvivoChem
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TargetMol Chemicals Inc.
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Zibo Hangyu Biotechnology Development Co., Ltd
+86-0533-2185556 +8617865335152 Mandy@hangyubiotech.com China 11013 58

AMG 900 Spectrum

N-[4-[[3-(2-Amino-4-pyrimidinyl)-2-pyridinyl]oxy]phenyl]-4-(4-methyl-2-thienyl)-1-phthalazinamine AMG 900 AMG 900 N-[4-[[3-(2-Amino-4-pyrimidinyl)-2-pyridinyl]oxy]phenyl]-4-(4-methyl-2-thienyl)-1-phthalazinamine N-(4-((3-(2-Aminopyrimidin-4-yl)pyridin-2-yl)oxy)phenyl)-4-(4-methylthiophen-2-yl)phthalazin-1 AMG-900;AMG900 1-Phthalazinamine, N-[4-[[3-(2-amino-4-pyrimidinyl)-2-pyridinyl]oxy]phenyl]-4-(4-methyl-2-thienyl)- AMG 900 USP/EP/BP 945595-80-2 C28H21N7OS C28H21N7O5 Inhibitor Inhibitors