research use only

6H05 Ras inhibitor

Cat.No.S7330

6H05 is a selective, and allosteric inhibitor of oncogenic K-Ras(G12C).
6H05 Ras inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 590.14

Quality Control

Batch: S733001 DMSO]100 mg/mL]false]Water]100 mg/mL]false]Ethanol]100 mg/mL]false Purity: 99.08%
99.08

Chemical Information, Storage & Stability

Molecular Weight 590.14 Formula

C20H30ClN3O2S3.CF3COOH

Storage (From the date of receipt)
CAS No. 2061344-88-3 Download SDF Storage of Stock Solutions

Synonyms N/A Smiles CN(C)CCSSCCNC(=O)C1CCN(CC1)C(=O)CSC2=CC=C(C=C2)Cl.C(=O)(C(F)(F)F)O

Solubility

In vitro
Batch:

DMSO : 100 mg/mL ( (169.45 mM) Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : 100 mg/mL

Ethanol : 100 mg/mL

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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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.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Mechanism of Action

Targets/IC50/Ki
K-Ras(G12C) [1]
In vitro
6H05 gives the greatest degree of modification, which allosterically modifies the oncogenic G12C mutant of highly homologous protein H-Ras without affecting wild-type K-Ras. [1]. Furthermore, this compound can be used as an intermediate for the synthesis of other oncogenic K-Ras(G12C) inhibitors. [2]
References

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