01 · Identity

One molecule, several searchable names.

Daraxonrasib is the generic name; RMC-6236is the development code found throughout early research and clinical-trial records. RASONQUE is the U.S. brand name for the finished prescription medicine from Revolution Medicines.

Generic namedaraxonrasib
Development codeRMC-6236
CAS Registry Number2765081-21-6
Molecular formulaC44H58N8O5S
Molecular weight811.0 g/mol
PubChem CID164726578
Verify the chemical record at PubChem

02 · RAS(ON) mechanism

Targeting the active, GTP-bound state of RAS.

Peer-reviewed work describes daraxonrasib as a non-covalent, multi-selective RAS(ON) inhibitor. The molecule first binds cyclophilin A (CypA); that binary complex then engages active, GTP-bound RAS to form a tri-complex. The assembled complex sterically blocks interactions between RAS and downstream effector proteins.

01Daraxonrasib

binds CypA

02Binary complex

engages RAS-GTP

03Tri-complex

blocks effector binding

This simplified research summary is not prescribing information and does not describe all pharmacology, safety, or clinical-use considerations.

Jiang et al., Cancer Discovery (2024)

03 · Regulatory status

The science moved from development code to approved ingredient.

United States · 26 August 2026

FDA approved daraxonrasib as RASONQUE.

The FDA approval notice identifies daraxonrasib (RASONQUE, Revolution Medicines, Inc.) for adults with metastatic pancreatic adenocarcinoma who have received at least one prior systemic therapy or who are not candidates for multiagent systemic therapy.

Read the FDA approval notice

Approval of a finished drug does not make bulk compound or research material interchangeable with the medicine. Patients and clinicians should use the official label and manufacturer channels; Daraxon does not provide medical advice or dispense RASONQUE.

04 · Daraxon research material

Defined for qualified R&D and registration workflows.

Daraxon’s offering is intended for professional organizations conducting chemical, analytical, formulation, nonclinical, process-development, or drug-registration work. A request should identify the intended use, quantity range, destination and documentation needs so suitability can be assessed before supply.

Research-use boundary

Not for personal purchase, self-administration, compounding, diagnosis, treatment, or any human use.

05 · Quality package

Batch evidence—not generic promises.

The target commercial specification is ≥99% purity by HPLC. The actual result, test methods and release decision must be taken from the Certificate of Analysis for the specific lot.

01

Certificate of Analysis

Identity, assay or purity, lot information and release data.

02

Chromatography

Batch-relevant HPLC documentation and method context where applicable.

03

Spectroscopy

NMR or other identity-supporting data available according to the supplied package.

04

Regulatory reference

Daraxon identifies its Type II U.S. Drug Master File as DMF 43871; verify current status directly with FDA.

FDA Drug Master File search

06 · FAQ

Common daraxonrasib questions.

What is daraxonrasib?

Daraxonrasib is the nonproprietary name of a RAS GTPase-family inhibitor. It was developed as RMC-6236 and is the active ingredient in the FDA-approved prescription medicine RASONQUE.

Are daraxonrasib and RMC-6236 the same compound?

Yes. RMC-6236 is the development code used in scientific papers and trial records; daraxonrasib is the generic name.

Is Daraxon selling RASONQUE?

No. RASONQUE is a finished prescription medicine from Revolution Medicines. Daraxon describes research/API material for qualified organizations and is not affiliated with Revolution Medicines.

Can Daraxon material be used in people?

No. Daraxon material is offered only for qualified research, analytical, or drug-registration work and is not for personal, diagnostic, therapeutic, or human use.