MedKoo Cat#: 462564 | Name: Revumenib free base
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

Revumenib (SNDX-5613) is an orally bioavailable, potent, and selective Menin-MLL (Mixed Lineage Leukemia) inhibitor designed to target MLL-rearranged (MLL-r) and NPM1-mutant acute leukemias. In preclinical models, Revumenib has demonstrated low nanomolar potency with an IC₅₀ of approximately 8–20 nM for disruption of the Menin-MLL interaction, leading to downregulation of HOXA9 and MEIS1 expression, which are critical oncogenic drivers.

Chemical Structure

Revumenib free base
Revumenib free base
CAS#2169919-21-3 (free base)

Theoretical Analysis

MedKoo Cat#: 462564

Name: Revumenib free base

CAS#: 2169919-21-3 (free base)

Chemical Formula: C32H47FN6O4S

Exact Mass: 630.3364

Molecular Weight: 630.82

Elemental Analysis: C, 60.93; H, 7.51; F, 3.01; N, 13.32; O, 10.14; S, 5.08

Price and Availability

Size Price Availability Quantity
25mg USD 450.00 2 Weeks
50mg USD 750.00 2 Weeks
100mg USD 1,250.00 2 Weeks
200mg USD 2,050.00 2 Weeks
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Synonym
SNDX-5613; SNDX 5613; SNDX5613; Revumenib;
IUPAC/Chemical Name
N-ethyl-2-((4-(7-(((1r,4r)-4-(ethylsulfonamido)cyclohexyl)methyl)-2,7-diazaspiro[3.5]nonan-2-yl)pyrimidin-5-yl)oxy)-5-fluoro-N-isopropylbenzamide
InChi Key
FRVSRBKUQZKTOW-YOCNBXQISA-N
InChi Code
InChI=1S/C32H47FN6O4S/c1-5-39(23(3)4)31(40)27-17-25(33)9-12-28(27)43-29-18-34-22-35-30(29)38-20-32(21-38)13-15-37(16-14-32)19-24-7-10-26(11-8-24)36-44(41,42)6-2/h9,12,17-18,22-24,26,36H,5-8,10-11,13-16,19-21H2,1-4H3/t24-,26-
SMILES Code
O=C(C1=CC(F)=CC=C1OC2=CN=CN=C2N3CC4(C3)CCN(CC4)C[C@H]5CC[C@@H](CC5)NS(=O)(CC)=O)N(C(C)C)CC
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO and ethanol
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info
Product Data
Biological target:
Revumenib is a potent and specific Menin-MLL inhibitor with a binding Ki of 0.149 nM and a cell based IC50 of 10-20 nM.
In vitro activity:
To be determined
In vivo activity:
Menin inhibitors, such as revumenib, have proven effective in patients with acute leukemias. A phase II study of revumenib yielded a response rate of 63% in patients with relapsed or refractory disease and KMT2A rearrangements. A phase I trial combining revumenib with three chemotherapies also yielded complete remissions in patients with acute myeloid leukemia. Reference: Cancer Discov. 2023 Dec 14:OF1. https://pubmed.ncbi.nlm.nih.gov/38096500/
Solvent mg/mL mM
Solubility
DMSO 25.0 39.63
Ethanol 25.0 39.63
Note: There can be variations in solubility for the same chemical from different vendors or different batches from the same vendor. The following factors can affect the solubility of the same chemical: solvent used for crystallization, residual solvent content, polymorphism, salt versus free form, degree of hydration, solvent temperature. Please use the solubility data as a reference only. Warming and sonication will facilitate dissolving. Still have questions? Please contact our Technical Support scientists.

Preparing Stock Solutions

The following data is based on the product molecular weight 630.82 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
1. Menin Inhibitors Trigger Leukemia Remissions. Cancer Discov. 2023 Dec 14:OF1. doi: 10.1158/2159-8290.CD-ND2023-0019. Epub ahead of print. PMID: 38096500. 2. Rasouli M, Blair H, Troester S, Szoltysek K, Cameron R, Ashtiani M, Krippner-Heidenreich A, Grebien F, McGeehan G, Zwaan CM, Heidenreich O. The MLL-Menin Interaction is a Therapeutic Vulnerability in NUP98-rearranged AML. Hemasphere. 2023 Jul 27;7(8):e935. doi: 10.1097/HS9.0000000000000935. PMID: 37520776; PMCID: PMC10378738.
In vitro protocol:
To be determined
In vivo protocol:
1. Menin Inhibitors Trigger Leukemia Remissions. Cancer Discov. 2023 Dec 14:OF1. doi: 10.1158/2159-8290.CD-ND2023-0019. Epub ahead of print. PMID: 38096500. 2. Rasouli M, Blair H, Troester S, Szoltysek K, Cameron R, Ashtiani M, Krippner-Heidenreich A, Grebien F, McGeehan G, Zwaan CM, Heidenreich O. The MLL-Menin Interaction is a Therapeutic Vulnerability in NUP98-rearranged AML. Hemasphere. 2023 Jul 27;7(8):e935. doi: 10.1097/HS9.0000000000000935. PMID: 37520776; PMCID: PMC10378738.
1: A drug, SNDX-5613, to treat acute leukemia with a KMT2A translocation or an NPM1 mutation that has come back (relapsed) or has not gotten better with treatment (refractory).