MedKoo Cat#: 414998 | Name: Pirinixil

Description:

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

Pirinixil is a hypolipidemic low toxicity agent.

Chemical Structure

Pirinixil
Pirinixil
CAS#65089-17-0

Theoretical Analysis

MedKoo Cat#: 414998

Name: Pirinixil

CAS#: 65089-17-0

Chemical Formula: C16H19ClN4O2S

Exact Mass: 366.0917

Molecular Weight: 366.86

Elemental Analysis: C, 52.38; H, 5.22; Cl, 9.66; N, 15.27; O, 8.72; S, 8.74

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.
Bulk Inquiry
Related CAS #
No Data
Synonym
Pirinixil; CCRIS134; CCRIS-134; CCRIS 134; BR931; BR 931; BR-931
IUPAC/Chemical Name
2-((4-Chloro-6-((2,3-dimethylphenyl)amino)-2-pyrimidinyl)thio)-N-(2-hydroxyethyl)acetamide
InChi Key
RZCKTPORLKUFGY-UHFFFAOYSA-N
InChi Code
InChI=1S/C16H19ClN4O2S/c1-10-4-3-5-12(11(10)2)19-14-8-13(17)20-16(21-14)24-9-15(23)18-6-7-22/h3-5,8,22H,6-7,9H2,1-2H3,(H,18,23)(H,19,20,21)
SMILES Code
O=C(NCCO)CSC1=NC(NC2=CC=CC(C)=C2C)=CC(Cl)=N1
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
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 366.86 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: D'Atri G, Gomarasca P, Galimberti E, Sirtori CR, Kritchevsky D. Clofibrate, pirinixil (BR 931) and WY-14,643 do not affect body cholesterol in Sprague- Dawley rats. Atherosclerosis. 1980 Nov;37(3):475-83. doi: 10.1016/0021-9150(80)90154-9. PMID: 7458993. 2: Kritchevsky D, Singer D, Klurfeld DM. Influence of hypocholesterolemic drugs on aortic cholesterol esterase in rabbits. Pharmacol Res Commun. 1984 Jun;16(6):525-31. doi: 10.1016/s0031-6989(84)80033-8. PMID: 6463093. 3: Lovati MR, De Marchi G. Plasma lipoprotein composition in cholesterol fed rabbits treated with pirinixil (BR 931), a new lipid lowering agent. Pharmacol Res Commun. 1981 Feb;13(2):133-9. doi: 10.1016/s0031-6989(81)80014-8. PMID: 7220573. 4: Najemnik C, Irsigler K, Sirtori CR. Pilot study of pirinixil (BR 931) in various forms of hyperlipoproteinemias. Pharmacol Res Commun. 1981 Sep;13(8):777-86. doi: 10.1016/s0031-6989(81)80096-3. PMID: 7027276. 5: Kritchevsky D, Klurfeld DM, Tepper SA, Mueller MA, Puglisi L, Sirtori CR. Increased plasma cholesterol and decreased body lipid levels in Wistar rats following pirinixil (BR 931) treatment. Pharmacol Res Commun. 1979 Jun;11(6):475-82. doi: 10.1016/s0031-6989(79)80019-3. PMID: 504321. 6: Simbula G, Pibiri M, Sanna L, Cossu C, Molotzu F, Columbano A, Ledda- Columbano GM. The peroxisome proliferator BR931 kills FaO cells by p53-dependent apoptosis. Life Sci. 2004 Jun 4;75(3):271-86. doi: 10.1016/j.lfs.2003.10.039. PMID: 15135649. 7: Shinozuka H, Abanobi SE, Lombardi B. Modulation of tumor promotion in liver carcinogenesis. Environ Health Perspect. 1983 Apr;50:163-8. doi: 10.1289/ehp.8350163. PMID: 6135607; PMCID: PMC1569229. 8: Eagon PK, Teepe AG, Elm MS, Tadic SD, Epley MJ, Beiler BE, Shinozuka H, Rao KN. Hepatic hyperplasia and cancer in rats: alterations in copper metabolism. Carcinogenesis. 1999 Jun;20(6):1091-6. doi: 10.1093/carcin/20.6.1091. PMID: 10357793. 9: Gupta C, Hattori A, Shinozuka H. Suppression of EGF binding in rat liver by the hypolipidemic peroxisome proliferators, 4-chloro-6-(2,3-xylidino)-2-pyrimidinylthio-(N-beta-hydroxyethyl)ac etamide and di(2-ethylhexyl)phthalate. Carcinogenesis. 1988 Jan;9(1):167-9. doi: 10.1093/carcin/9.1.167. PMID: 3257172. 10: Ohmura T, Ledda-Columbano GM, Piga R, Columbano A, Glemba J, Katyal SL, Locker J, Shinozuka H. Hepatocyte proliferation induced by a single dose of a peroxisome proliferator. Am J Pathol. 1996 Mar;148(3):815-24. PMID: 8774136; PMCID: PMC1861716.