ChemicalBook > Product Catalog >API >Inhibitors >Sotorasib

Sotorasib

Sotorasib Structure
CAS No.
2296729-00-3
Chemical Name:
Sotorasib
Synonyms
Sotorasib;AMG-510(Sotorasib);Storasib;Sotoracib;rac AMG-510;CID 137278711;2H7]-Sotorasib;Sotolabu (AMG-510);Sotorasib AMG510 AMG-510;Sotorasib, 10 mM in DMSO
CBNumber:
CB65475731
Molecular Formula:
C30H30F2N6O3
Molecular Weight:
560.61
MOL File:
2296729-00-3.mol
Modify Date:
2025/4/28 21:36:36

Sotorasib Properties

Boiling point 730.5±70.0 °C(Predicted)
Density 1.36±0.1 g/cm3(Predicted)
storage temp. Store at -20°C, stored under nitrogen
solubility DMSO : 100 mg/mL (178.38 mM; Need ultrasonic)|
pka 6.52±0.35(Predicted)
form Solid
color White to yellow
Water Solubility Water : 33.33 mg/mL (59.46 mM; ultrasonic and adjust pH to 11 with NaOH)
InChIKey NXQKSXLFSAEQCZ-UHFFFAOYSA-N
SMILES O=C1N=C(N2CCN(C(=O)C=C)CC2C)C2=CC(F)=C(C3C(=CC=CC=3F)O)N=C2N1C1C(=CC=NC=1C(C)C)C

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

Sotorasib Chemical Properties,Uses,Production

brand name

Lumakras

General Description

Sotorasib, also known as AMG-510, is an acrylamide derived KRAS inhibitor developed by Amgen. It is indicated in the treatment of adult patients with KRAS G12C mutant non small cell lung cancer. This mutation makes up >50% of all KRAS mutations. Mutant KRAS discovered in 1982 but was not considered a druggable target until the mid-2010s. It is the first experimental KRAS inhibitor. The drug [MRTX849] is also currently being developed and has the same target. Sotorasib was granted FDA approval on 28 May 2021.

General Description

Class: non-kinase; Treatment: KRAS(G12C) NSCLC; Other name: AMG 510; Elimination half-life: 5.5 h; Protein binding = 89%

Side effects

Sotorasib may cause breathing problems that could lead to death. Get emergency medical help if you have new or worsening fever, cough, or shortness of breath.
Common side effects may include:
nausea, diarrhea;
cough;
liver problems;
pain in your bones, joints, or muscles;
tiredness;
abnormal lab tests.
For 28 patients (22%), side effects led to a pause, a reduction, or both, in the dose of sotorasib. Nine people (7%) stopped the treatment because of side effects.
www.everydayhealth.com/drugs/sotorasib

target

Primary target: KRAS(G12C)

Mode of action

Sotorasib is an orally available inhibitor of the specific KRAS mutation, p.G12C, with potential antineoplastic activity. Upon oral administration, sotorasib selectively targets, binds to and inhibits the activity of the KRAS p.G12C mutant. This may inhibit growth in KRAS p.G12C-expressing tumor cells. The KRAS p.G12C mutation is seen in some tumor cell types and plays a key role in tumor cell proliferation.

Sotorasib Preparation Products And Raw materials

Raw materials

Preparation Products

Sotorasib Suppliers

Global( 218)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Bulat Pharmaceutical Pvt Ltd +91-8448085659 +91-8448085660 Haryana, India 123 58 Inquiry
Aspen Biopharma Labs Pvt Ltd +91-9248058660 +91-9248058662 Telangana, India 234 58 Inquiry
ENBRIDGE PHARMTECH CO., LTD. +8613812269233 China 322 58 Inquiry
Heading (Nanjing)Pharmtechnologies Co., Ltd. +86-25-58467899-832 +86-13382406280 China 46 58 Inquiry
Tianjin Kilo Pharmaceutical Sci-Tech Co., Ltd +86-02223869539 +86-15560057295 China 27 58 Inquiry
ATK CHEMICAL COMPANY LIMITED +undefined-21-51877795 China 33024 60 Inquiry
Jinan Carbotang Biotech Co.,Ltd. +8615866703830 China 8497 58 Inquiry
CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49732 58 Inquiry
Chengdu Aslee Biopharmaceuticals, Inc. 28-85305008 CHINA 964 58 Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 +1-00000000000 United States 32222 58 Inquiry

Related articles

  • How is Sotorasib synthesised?
  • The synthetic route of Sotorasib is completed in three steps, starting with the amidation of nicotinic acid derivatives to pro....
  • Jan 26,2024

Sotorasib Spectrum

2296729-00-3(Sotorasib)Related Search:

PYRIDO[2,3-D]PYRIMIDIN-2(1H)-ONE, 6-FLUORO-7-(2-FLUORO-6-HYDROXYPHENYL)-1-[4-METHYL-2-(1-METHYLETHYL Pyrido[2,3-d]pyrimidin-2(1H)-one, 6-fluoro-7-(2-fluoro-6-hydroxyphenyl)-1-[4-methyl-2-(1-methylethyl)-3-pyridinyl]-4-[(2S)-2-methyl-4-(1-oxo-2-propen-1-yl)-1-piperazinyl]-, (1R)- 6-fluoro-7-(2-fluoro-6-hydroxyphenyl)-1-(4-methyl-2-propan-2-ylpyridin-3-yl)-4-[(2S)-2-methyl-4-prop-2-enoylpiperazin-1-yl]pyrido[2,3-d]pyrimidin-2-one CID 137278711 Pyrido[2,3-d]pyrimidin-2(1H)-one, 6-fluoro-7-(2-fluoro-6-hydroxyphenyl)-1-[4-methyl-2-(1-methylethyl)-3-pyridinyl]-4-[(2S)-2-methyl-4-(1-oxo-2-propen-1-yl)-1-piperazinyl]-, (1R)- 6-fluoro-7-(2-fluoro-6-hydroxyphenyl)-1-(4-methyl-2-propan-2-ylpyridin-3-yl)-4-[(2S)-2-methyl-4-prop-2-enoylpiperazin-1-yl]pyrido[2,3-d]pyrimidin-2-one Storasib AMG-510(Sotorasib) Sotorasib Pyrido[2,3-d]pyrimidin-2(1H)-one, 6-fluoro-7-(2-fluoro-6-hydroxyphenyl)-1-[4-methyl-2-(1-methylethyl)-3-pyridinyl]-4-[(2S)-2-methyl-4-(1-oxo-2-propen-1-yl)-1-pi 2H7]-Sotorasib (1R)-6-fluoro-7-(2-fluoro-6-hydroxy-phenyl)-1-(2-isopropyl-4-methyl-3-pyridyl)-4-[(2S)-2-methyl-4-prop-2-enoyl-piperazin-1-yl]pyrido[2,3-d]pyrimidin-2-one (1R)-4-((S)-4-Acryloyl-2-methylpiperazin-1-yl)-6-fluoro-7-(2-fluoro-6-hydroxyphenyl)-1-(2-isopropyl-4-methylpyridin-3-yl)pyrido[2,3-d]pyrimidin-2(1H)-one 4-(4-acryloyl-2-methylpiperazin-1-yl)-6-fluoro-7-(2-fluoro-6-hydroxyphenyl)-1-(2-isopropyl-4-methylpyridin-3-yl)pyrido[2,3-d]pyrimidin-2(1H)-one rac AMG-510 Sotoracib Sotorasib AMG510 AMG-510 Sotolabu (AMG-510) Sotorasib, 10 mM in DMSO 2296729-00-3 API 2296729-00-3