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research use only
Cat.No.S8830
| Related Targets | CDK HSP PD-1/PD-L1 ROCK Wee1 DNA/RNA Synthesis Microtubule Associated Ras Aurora Kinase Casein Kinase |
|---|---|
| Other K-Ras Products | Adagrasib (MRTX849) MRTX1133 BI-2852 RMC-7977 HRS-4642 Daraxonrasib (RMC-6236) Zoldonrasib (RMC-9805) ARS-1620 ARS-853 BI-3406 |
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In vitro |
DMSO
: 100 mg/mL
(178.38 mM)
Ethanol : 13 mg/mL Water : Insoluble |
|
In vivo |
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Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
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Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
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| Molecular Weight | 560.59 | Formula | C30H30F2N6O3 |
Storage (From the date of receipt) | 3 years -20°C powder |
|---|---|---|---|---|---|
| CAS No. | 2296729-00-3 | -- | Storage of Stock Solutions |
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| Synonyms | N/A | Smiles | CC1CN(CCN1C2=NC(=O)N(C3=NC(=C(C=C32)F)C4=C(C=CC=C4F)O)C5=C(C=CN=C5C(C)C)C)C(=O)C=C | ||
| Targets/IC50/Ki |
K-Ras(G12C)
|
|---|---|
| In vitro |
Sotorasib (AMG510) inhibits SOS1-catalyzed nucleotide exchange of recombinant mutant KRAS (G12C/C118A) but had minimal effect on KRAS (C118A). It also selectively impairs the viability of KRAS p.G12C mutant lines but does not affect cell lines with other KRAS mutations. |
| In vivo |
In preclinical tumor models, Sotorasib (AMG510) rapidly and irreversibly binds to KRAS (G12C), providing durable suppression of the mitogen-activated protein kinase (MAPK) signaling pathway. Dosed orally (once daily) as a single agent, it is capable of inducing tumor regression in mouse models of KRASG12C cancer. |
References |
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| Methods | Biomarkers | Images | PMID |
|---|---|---|---|
| Western blot | ERK EGFR / AKT / MEK / ERK / Vinculin EGFR / RAS / MEK / DUSP6 / CyclinD1 / Vinculin pMEK / pERK / pAKT / HSP90 |
|
32430388 |
(data from https://clinicaltrials.gov, updated on 2024-05-22)
| NCT Number | Recruitment | Conditions | Sponsor/Collaborators | Start Date | Phases |
|---|---|---|---|---|---|
| NCT06061523 | Withdrawn | Healthy Participants |
Amgen |
July 15 2024 | Phase 1 |
| NCT05920356 | Recruiting | Non-Small Cell Lung Cancer (NSCLC) |
Amgen |
November 16 2023 | Phase 3 |
| NCT06314763 | Completed | Drug Drug Interaction Study |
Radboud University Medical Center|Amgen |
November 9 2023 | Phase 4 |
| NCT05497557 | Completed | Healthy Volunteers |
Amgen |
July 14 2022 | Phase 1 |
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