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Adagrasib

CAS No.
2326521-71-3
Chemical Name:
Adagrasib
Synonyms
Adagrasib;MRTX-849;2-((S)-4-(7-(8-chloronaphthalen-1-yl)-2-(((S)-1-methylpyrrolidin-2-yl)methoxy)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4-yl)-1-(2-fluoroacryloyl)piperazin-2-yl)acetonitrile;Adarese;MTRX-849;Agdarcy step;CAS:2326521-71-3;Adagrasib/MRTX-849;MRTX849(Adagrasib);Azvudine Impurity 23
CBNumber:
CB94918285
Molecular Formula:
C32H35ClFN7O2
Molecular Weight:
604.12
MDL Number:
MFCD32263433
MOL File:
2326521-71-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 06:10:33

Adagrasib Properties

Boiling point 860.2±75.0 °C(Predicted)
Density 1.295±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO:1.0(Max Conc. mg/mL);1.7(Max Conc. mM)
form A crystalline solid
pka 9.31±0.40(Predicted)
color White to yellow
InChIKey PEMUGDMSUDYLHU-ZEQRLZLVSA-N
SMILES N1(C(=O)C(F)=C)CCN(C2N=C(OC[C@@H]3CCCN3C)N=C3CN(C4=C5C(C=CC=C5Cl)=CC=C4)CCC3=2)C[C@@H]1CC#N
FDA UNII 8EOO6HQF8Y

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P280-P301+P312-P302+P352-P305+P351+P338
NFPA 704
0
2 0

Adagrasib price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 31440 MRTX-849 ≥98% 2326521-71-3 1mg $49 2026-04-30 Buy
Cayman Chemical 31440 MRTX-849 ≥98% 2326521-71-3 5mg $182 2026-04-30 Buy
Cayman Chemical 31440 MRTX-849 ≥98% 2326521-71-3 10mg $291 2026-04-30 Buy
Biosynth BM177692 MRTX849 2326521-71-3 5mg $371.1 2026-06-04 Buy
Biosynth BM177692 MRTX849 2326521-71-3 10mg $630.9 2026-06-04 Buy
Product number Packaging Price Buy
31440 1mg $49 Buy
31440 5mg $182 Buy
31440 10mg $291 Buy
BM177692 5mg $371.1 Buy
BM177692 10mg $630.9 Buy

Adagrasib Chemical Properties, Uses, Production

Description

MRTX-849 was identified as a potent, selective, and covalent KRASG12C inhibitor that exhibits favourable drug-like properties, modifies mutant cysteine 12 in GDP-bound KRASG12C, and inhibits KRAS-dependent signalling. MRTX-849 demonstrated pronounced tumour regression in 17 of 26 (65%) KRASG12C-positive cell line- and patient-derived xenograft models from multiple tumour types, and objective responses have been observed in patients with KRASG12C-positive lung and colon adenocarcinomas[1].

Uses

MRTX 849 is used as combination therapy for treatment of cancer.

Definition

Adagrasib is an orally available, potent, irreversible, small molecule inhibitor of KRAS G12C mutant isoform being developed by Mirati Therapeutics for the treatment of solid tumours harbouring KRAS G12C oncogenic driver mutation, including non-small cell lung cancer (NSCLC) and colorectal cancer (CRC).

brand name

Krazati

General Description

Class: non-kinase; Treatment: KRAS(G12C) NSCLC; Other name: MRTX849; Elimination half-life: 24 h; Protein binding = 98.3%

Biological Activity

To minimize GSH metabolism, the development candidate MRTX-849 employed a 2-fluoroacrylamide warhead, imparting whole blood stability of >50 h t1/2 across species while maintaining tractable cellular potency (IC50 = 5–14 nM). Metabolism studies of MRTX-849 in hepatocytes showed that GSH conjugation of the 2-fluoroacrylamide was reduced compared to previous analogues containing the unsubstituted acrylamide. Favorable in vitro ADME and physical properties of MRTX-849 translated into moderate to high bioavailability of 26–63% across species tested. In a PK/PD experiment dosed at 10, 30, and 100 mg/kg to NCI-H358 tumor-bearing mice, MRTX-849 demonstrated dose-dependent protein modification with nearly maximal effect at the highest doses[2].

Mechanism of action

Adagrasib selectively modified mutant cysteine 12 in GDP-bound G12C and inhibited KRASdependent signaling.

Pharmacokinetics

The specifc KRAS G12C inhibitor MRTX849 inhibits the drug efux function of ABCB1 protein by interacting with the nucleotide binding domain of ABCB1, thereby increasing intracellular anticancer drug concentrations and overcoming MDR. While MRTX849 has attracted a lot of attention as a specifc KRAS G12C inhibitor for the treatment of KRAS-dependent tumors, this study revealed that MRTX849 may also be applied in combination with conventional chemotherapeutic agents for overcoming MDR.

Clinical Use

Adagrasib is an irreversible inhibitor of the RAS GTPase family. It is approved by the FDA for the treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) who have been identified by testing as having a KRAS (G12C) mutation.

Synthesis

Boc deprotection was achieved by treatment with hydrochloric acid, and the resulting deprotected amine (19.5) crystallized as the tartrate salt in 80% isolated yield. Compound 19.5 was then coupled with naphthyl bromide 19.6 as the free base via the Buchwald-Hartwig reaction, and product 19.7 crystallized as the p-toluenesulfonate salt and was isolated in 71% yield. To avoid the complications caused by the potential mutagenic impurities and retro-Michael products that may be generated by the conventional carboxybenzoyl deprotection protocol, the authors developed a novel nucleophilic deprotection reaction using 2-mercaptoethanol and potassium phosphate in DMA. This approach afforded the deprotected piperazine 19.8 with minimal racemization, affording the crystalline product in 86% isolated yield. Finally, the cysteine-active warhead was introduced by coupling sodium 2-fluoroacrylate 19.9 with piperazine 19.8 using T3P (propylphosphonic anhydride) in acetonitrile, and Adagrasib (19) was isolated in 70% yield after two consecutive recrystallizations.
Adagrasib

target

Primary target: KRAS(G12C)

storage

Store at -20°C

References

[1] Jay B. Fell. “Identification of the Clinical Development Candidate MRTX849, a Covalent KRASG12C Inhibitor for the Treatment of Cancer.” Journal of Medicinal Chemistry 63 13 (2020): 6679–6693.
[2] J. Christensen. “The KRASG12C Inhibitor, MRTX849, Provides Insight Toward Therapeutic Susceptibility of KRAS Mutant Cancers in Mouse Models and Patients.” Cancer discovery (2019).

Adagrasib Preparation Products And Raw materials

Raw materials

Preparation Products

Adagrasib Suppliers

Global Suppliers ( 201)
Supplier Tel Email Country ProdList Advantage
Cangzhou Enke Pharma-tech Co., Ltd. 0317-5296180 15533709196 enkepharma@126.com China 2495 55
ShangHai Biochempartner Co.,Ltd 177-54423994 17754423994 2853530910@QQ.com China 8000 62
ShangHai ChuanQian Chemcial Technique Centre 15869524721 3525679403@qq.com China 4565 58
Changzhou Yongfeng Biomedicine Co. Ltd. 15006117673 2973592490@qq.com China 271 58
Jinan Cen Ben Medical Technology Co., Ltd 14793566 info@cenpharm.com China 785 58
Changzhou Borl Biotechnology Co.,LTD 13656121842 luyan0021@163.com China 265 58
Wuhan Jingkangen Biomedical Technology Co., Ltd 13720134139 086-15871494362 13720134139 orders@jknbiochem.com China 7283 58
Cangzhou Kangrui Medical Technology Co., LTD 18632776803 cangzhoukangrui@126.com;355803330@qq.com China 679 58
Beijing Ouhe Technology Co., Ltd 13552068683 13522913783 2355560935@qq.com China 11777 60
ChengDu TongChuangYuan Pharmaceutical Co.Ltd 28-83379370 13880556291 tcy@tcypharm.com China 509 57

View Latest Price from Adagrasib manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Adagrasib pictures 2026-09-18 Adagrasib
2326521-71-3
1g More Than 99% 100kg/Month BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD.
Adagrasib. pictures 2026-09-18 Adagrasib.
2326521-71-3
1g More Than 99% 100kg/Month BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD.
MRTX-849 pictures 2026-06-30 MRTX-849
2326521-71-3
1kg 99% 10000KGS Shaanxi Dideu New Materials Co. Ltd
  • Adagrasib pictures
  • Adagrasib
    2326521-71-3
  • $0.00
  • More Than 99%
  • BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD.
  • Adagrasib. pictures
  • Adagrasib.
    2326521-71-3
  • $0.00
  • More Than 99%
  • BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD.
  • MRTX-849 pictures
  • MRTX-849
    2326521-71-3
  • $0.00
  • 99%
  • Shaanxi Dideu New Materials Co. Ltd

Adagrasib Spectrum

MRTX849;MRTX-849;MRTX 849 2-PIPERAZINEACETONITRILE, 4-[7-(8-CHLORO-1-NAPHTHALENYL)-5,6,7,8-TETRAHYDRO-2-[[(2S)-1-METHYL-2-PYRR 2-Piperazineacetonitrile, 4-[7-(8-chloro-1-naphthalenyl)-5,6,7,8-tetrahydro-2-[[(2S)-1-methyl-2-pyrrolidinyl]methoxy]pyrido[3,4-d]pyrimidin-4-yl]-1-(2-fluoro-1-oxo-2-propen-1-yl)-, (2S)- 2-[(2S)-4-[7-(8-chloronaphthalen-1-yl)-2-[[(2S)-1-methylpyrrolidin-2-yl]methoxy]-6,8-dihydro-5H-pyrido[3,4-d]pyrimidin-4-yl]-1-(2-fluoroprop-2-enoyl)piperazin-2-yl]acetonitrile MRTX849(Adagrasib) Adagrasib/MRTX-849 Adagrasib 4-[7-(8-CHLORO-1-NAPHTHALENYL)-5,6,7,8-TETRAHYDRO-2-[[(2S)-1-METHYL-2-PYRR inhibit,GDP-bound,mutant,MIA PaCa-2,MRTX-849,Adagrasib,selective,Inhibitor,MRTX 849,inactive,state,G12C,H1373,covalent,anti-tumor,KRAS,Ras,cells 2-PIPERAZINEACETONITRILE,4-[7-(8-CHLORO-1-NAPHTHALENYL)-5,Chemicalbook6,7,8-TETRAHYDRO-2-[[(2S)-1-METHYL-2-PYRR 2-[(S)-4-[7-(8-chloro-1-naphthyl)-2-[[(S)-1-methyl-2-pyrrolidinyl]methoxy]-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4-yl]-1-(2-fluoroacryloyl)-2-piperazinyl]acetonitrile MTRX-849 Azvudine Impurity 23 Adarese Agdarcy step Adagrasib, 10 mM in DMSO CAS:2326521-71-3 2-((S)-4-(7-(8-chloronaphthalen-1-yl)-2-(((S)-1-methylpyrrolidin-2-yl)methoxy)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4-yl)-1-(2-fluoroacryloyl)piperazin-2-yl)acetonitrile MRTX-849 (2S)-4-[7-(8-Chloro-1-naphthalenyl)-5,6,7,8-tetrahydro-2-[[(2S)-1-methyl-2-pyrrolidinyl]methoxy]pyrido[3,4-d]pyrimidin-4-yl]-1-(2-fluoro-1-oxo-2-propen-1-yl)-2-piperazineacetonitrile (ACI) 2326521-71-3 2247859-59-1 api 2326521-71-3