MedKoo Cat#: 575763 | Name: Denfivontinib HCl

Description:

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

Denfivontinib, also known as G-749, is a novel, orally available FLT3 inhibitor. It selectively targets both FLT3 internal tandem duplication (ITD) and tyrosine kinase domain (TKD) mutations, including FLT3-D835, with nanomolar potency (IC₅₀ values typically <10 nM). Preclinical studies demonstrated that G-749 induces apoptosis and inhibits proliferation in FLT3-mutant AML cell lines and primary patient samples. It also showed strong anti-leukemic activity in FLT3-ITD xenograft mouse models, significantly reducing tumor burden and prolonging survival. Mechanistically, G-749 promotes degradation of FLT3 via disruption of chaperone protein interactions, in addition to kinase inhibition.

Chemical Structure

Denfivontinib HCl
Denfivontinib HCl
CAS#1457983-33-3 (HCl)

Theoretical Analysis

MedKoo Cat#: 575763

Name: Denfivontinib HCl

CAS#: 1457983-33-3 (HCl)

Chemical Formula: C25H26BrClN6O2

Exact Mass: 556.0989

Molecular Weight: 557.88

Elemental Analysis: C, 53.82; H, 4.70; Br, 14.32; Cl, 6.35; N, 15.06; O, 5.74

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Synonym
G-749 hydrochloride; G-749 HCl; G749 HCl; G 749 HCl; Denfivontinib hydrochloride; Denfivontinib HCl;
IUPAC/Chemical Name
8-bromo-2-((1-methylpiperidin-4-yl)amino)-4-((4-phenoxyphenyl)amino)pyrido[4,3-d]pyrimidin-5(6H)-one hydrochloride
InChi Key
UDYYCTJUUMIMHX-UHFFFAOYSA-N
InChi Code
InChI=1S/C25H25BrN6O2.ClH/c1-32-13-11-17(12-14-32)29-25-30-22-20(26)15-27-24(33)21(22)23(31-25)28-16-7-9-19(10-8-16)34-18-5-3-2-4-6-18;/h2-10,15,17H,11-14H2,1H3,(H,27,33)(H2,28,29,30,31);1H
SMILES Code
O=C1NC=C(C2=NC(NC3CCN(CC3)C)=NC(NC4=CC=C(C=C4)OC5=CC=CC=C5)=C21)Br.[H]Cl
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
Shelf Life
>2 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

Preparing Stock Solutions

The following data is based on the product molecular weight 557.88 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
1: Lee HK, Kim HW, Lee IY, Lee J, Lee J, Jung DS, Lee SY, Park SH, Hwang H, Choi JS, Kim JH, Kim SW, Kim JK, Cools J, Koh JS, Song HJ. G-749, a novel FLT3 kinase inhibitor, can overcome drug resistance for the treatment of acute myeloid leukemia. Blood. 2014 Apr 3;123(14):2209-19. doi: 10.1182/blood-2013-04-493916. Epub 2014 Feb 14. PubMed PMID: 24532805; PubMed Central PMCID: PMC3975259.