MedKoo Cat#: 124670 | Name: Venadaparib HCl

Description:

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

Venadaparib, also known as IDX-1197, is a potent, selective and orally active PARP inhibitor with IC50s of 1 ~2 nM.. By inhibiting PARP, IDX-1197 stops cancer cells from repairing SSBs and drives the conversion of SSBs into double-strand breaks. IDX-1197 triggers a phenomenon known as synthetic lethality, which is defined by cell death resulting from the simultaneous perturbation of two genes without damaging normal cells. IDX-1197 is primarily aimed at treating homologous recombination deficient (HRD) patients. Notably, IDX-1197 has a particularly strong trapping effect, meaning it is more effective at trapping PARP1 and PARP2 enzymes on damaged DNA.

Chemical Structure

Venadaparib HCl
Venadaparib HCl
CAS#1681020-60-9 (HCl)

Theoretical Analysis

MedKoo Cat#: 124670

Name: Venadaparib HCl

CAS#: 1681020-60-9 (HCl)

Chemical Formula: C23H24ClFN4O2

Exact Mass: 0.0000

Molecular Weight: 442.92

Elemental Analysis: C, 62.37; H, 5.46; Cl, 8.00; F, 4.29; N, 12.65; O, 7.22

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
Venadaparib hydrochloride; Venadaparib (hydrochloride); Venadaparib; IDX-1197; IDX 1197; IDX1197;
IUPAC/Chemical Name
4-(3-(3-((cyclopropylamino)methyl)azetidine-1-carbonyl)-4-fluorobenzyl)phthalazin-1(2H)-one hydrochloride
InChi Key
FSVSACOGQQIXAF-UHFFFAOYSA-N
InChi Code
InChI=1S/C23H23FN4O2.ClH/c24-20-8-5-14(10-21-17-3-1-2-4-18(17)22(29)27-26-21)9-19(20)23(30)28-12-15(13-28)11-25-16-6-7-16;/h1-5,8-9,15-16,25H,6-7,10-13H2,(H,27,29);1H
SMILES Code
C1CC1NCC2CN(C2)C(=O)C3=C(C=CC(=C3)CC4=NNC(=O)C5=CC=CC=C54)F.Cl
Appearance
To be determined
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
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
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 442.92 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 M, Je IG, Kim JE, Yoo Y, Lim JH, Jang E, Lee Y, Song DK, Moon AN, Kim JA, Jeong J, Park JT, Lee JW, Yang JH, Hong CH, Park SY, Park YW, Baek NS, Lee S, Ha KS, Choi S, Lee WS. Venadaparib Is a Novel and Selective PARP Inhibitor with Improved Physicochemical Properties, Efficacy, and Safety. Mol Cancer Ther. 2023 Mar 2;22(3):333-342. doi: 10.1158/1535-7163.MCT-22-0068. PMID: 36808277; PMCID: PMC9978881. 2: Kim HC, Yang E, Lee S, Oh J, Lee M, Lee C, Ha KS, Lee WS, Jang IJ, Yu KS. Effects of food and ethnicity on the pharmacokinetics of venadaparib, a next- generation PARP inhibitor, in healthy Korean, Caucasian, and Chinese male subjects. Invest New Drugs. 2024 Feb;42(1):80-88. doi: 10.1007/s10637-023-01405-z. Epub 2023 Dec 15. PMID: 38099989; PMCID: PMC10891214. 3: Chen L, Han W, Jing W, Feng M, Zhou Q, Cheng X. Novel anti-Acanthamoeba effects elicited by a repurposed poly (ADP-ribose) polymerase inhibitor AZ9482. Front Cell Infect Microbiol. 2024 May 28;14:1414135. doi: 10.3389/fcimb.2024.1414135. PMID: 38863831; PMCID: PMC11165085. 4: WHO Drug Information, Vol. 34, No. 2, 2020