MedKoo Cat#: 328406 | Name: Pinacidil

Description:

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

Pinacidil, also known as P-1134 and S-1230, is a guanidine that opens potassium channels producing direct peripheral vasodilatation of the arterioles. It reduces blood pressure and peripheral resistance and produces fluid retention.

Chemical Structure

Pinacidil
Pinacidil
CAS#60560-33-0

Theoretical Analysis

MedKoo Cat#: 328406

Name: Pinacidil

CAS#: 60560-33-0

Chemical Formula: C13H19N5

Exact Mass: 245.1640

Molecular Weight: 245.33

Elemental Analysis: C, 63.65; H, 7.81; N, 28.55

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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Related CAS #
No Data
Synonym
Pinacidil; P-1134; P 1134; P1134; S-1230; S 1230; S1230
IUPAC/Chemical Name
(Z)-2-cyano-1-(3,3-dimethylbutan-2-yl)-3-(pyridin-4-yl)guanidine
InChi Key
IVVNZDGDKPTYHK-UHFFFAOYSA-N
InChi Code
InChI=1S/C13H19N5/c1-10(13(2,3)4)17-12(16-9-14)18-11-5-7-15-8-6-11/h5-8,10H,1-4H3,(H2,15,16,17,18)
SMILES Code
CC(C)(C)C(N/C(NC1=CC=NC=C1)=N/C#N)C
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 245.33 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: Friedel HA, Brogden RN. Pinacidil. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in the treatment of hypertension. Drugs. 1990 Jun;39(6):929-67. Review. PubMed PMID: 2196168. 2: Ahnfelt-Rønne I. Pinacidil. Preclinical investigations. Drugs. 1988;36 Suppl 7:4-9. Review. PubMed PMID: 3076134. 3: Cohen ML, Kurz KD. Pinacidil-induced vascular relaxation: comparison to other vasodilators and to classical mechanisms of vasodilation. J Cardiovasc Pharmacol. 1988;12 Suppl 2:S5-9. PubMed PMID: 2466179. 4: Zushida K, Onodera K, Kamei J. Effect of diabetes on pinacidil-induced antinociception in mice. Eur J Pharmacol. 2002 Oct 25;453(2-3):209-15. PubMed PMID: 12398906. 5: Nakashima M, Li Y, Seki N, Kuriyama H. Pinacidil inhibits neuromuscular transmission indirectly in the guinea-pig and rabbit mesenteric arteries. Br J Pharmacol. 1990 Nov;101(3):581-6. PubMed PMID: 1963799; PubMed Central PMCID: PMC1917751. 6: Gollasch M, Bychkov R, Ried C, Behrendt F, Scholze S, Luft FC, Haller H. Pinacidil relaxes porcine and human coronary arteries by activating ATP-dependent potassium channels in smooth muscle cells. J Pharmacol Exp Ther. 1995 Nov;275(2):681-92. PubMed PMID: 7473155. 7: Levin RM, Hayes L, Zhao Y, Wein AJ. Effect of pinacidil on spontaneous and evoked contractile activity. Pharmacology. 1992;45(1):1-8. PubMed PMID: 1354875. 8: Gribble FM, Reimann F, Ashfield R, Ashcroft FM. Nucleotide modulation of pinacidil stimulation of the cloned K(ATP) channel Kir6.2/SUR2A. Mol Pharmacol. 2000 Jun;57(6):1256-61. PubMed PMID: 10825398. 9: Choi EM, Jung WW, Suh KS. Pinacidil protects osteoblastic cells against antimycin A-induced oxidative damage. Mol Med Rep. 2015 Jan;11(1):746-52. doi: 10.3892/mmr.2014.2721. Epub 2014 Oct 21. PubMed PMID: 25334089. 10: Goldberg MR, Rockhold FW, Thompson WL, DeSante KA. Clinical pharmacokinetics of pinacidil, a potassium channel opener, in hypertension. J Clin Pharmacol. 1989 Jan;29(1):33-40. PubMed PMID: 2708546.