MedKoo Cat#: 413495 | Name: Debrisoquine Free Base

Description:

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

Debrisoquine Free Base is an adrenergic neuron-blocking drug similar in effects to GUANETHIDINE. It is also noteworthy in being a substrate for a polymorphic cytochrome P-450 enzyme. Persons with certain isoforms of this enzyme are unable to properly metabolize this and many other clinically important drugs. They are commonly referred to as having a debrisoquin 4-hydroxylase polymorphism.

Chemical Structure

 Debrisoquine Free Base
Debrisoquine Free Base
CAS#1131-64-2 (free base)

Theoretical Analysis

MedKoo Cat#: 413495

Name: Debrisoquine Free Base

CAS#: 1131-64-2 (free base)

Chemical Formula: C10H13N3

Exact Mass: 175.1109

Molecular Weight: 175.24

Elemental Analysis: C, 68.54; H, 7.48; N, 23.98

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
Debrisoquine Free Base; Tendor; Debrisoquinum; Debrisoquin; Debrisoquine; Isocaramidine;
IUPAC/Chemical Name
2(1H)-Isoquinolinecarboximidamide, 3,4-dihydro-
InChi Key
JWPGJSVJDAJRLW-UHFFFAOYSA-N
InChi Code
InChI=1S/C10H13N3/c11-10(12)13-6-5-8-3-1-2-4-9(8)7-13/h1-4H,5-7H2,(H3,11,12)
SMILES Code
N=C(N1CC2=C(C=CC=C2)CC1)N
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
Solvent mg/mL mM
Solubility
To be determined 0.0 100.00
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 175.24 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: Idle JR, Mahgoub A, Angelo MM, Dring LG, Lancaster R, Smith RL. The metabolism of [14C]-debrisoquine in man. Br J Clin Pharmacol. 1979 Mar;7(3):257-66. doi: 10.1111/j.1365-2125.1979.tb00930.x. PMID: 371651; PMCID: PMC1429493. 2: Meyer UA, Skoda RC, Zanger UM. The genetic polymorphism of debrisoquine/sparteine metabolism-molecular mechanisms. Pharmacol Ther. 1990;46(2):297-308. doi: 10.1016/0163-7258(90)90096-k. PMID: 2181495. 3: Lennard MS. Genetic polymorphism of sparteine/debrisoquine oxidation: a reappraisal. Pharmacol Toxicol. 1990 Oct;67(4):273-83. doi: 10.1111/j.1600-0773.1990.tb00830.x. PMID: 2077517. 4: Cooke BR, Bligh SW, Cybulski ZR, Ioannides C, Hall M. Debrisoquine metabolism and CYP2D expression in marmoset liver microsomes. Drug Metab Dispos. 2012 Jan;40(1):70-5. doi: 10.1124/dmd.111.041566. Epub 2011 Oct 5. PMID: 21976620. 5: Spina E, Martines C, Caputi AP, Cobaleda J, Piñas B, Carrillo JA, Benitez J. Debrisoquine oxidation phenotype during neuroleptic monotherapy. Eur J Clin Pharmacol. 1991;41(5):467-70. doi: 10.1007/BF00626371. PMID: 1684751. 6: Eichelbaum M, Gross AS. The genetic polymorphism of debrisoquine/sparteine metabolism--clinical aspects. Pharmacol Ther. 1990;46(3):377-94. doi: 10.1016/0163-7258(90)90025-w. PMID: 2188269. 7: Jarema M. Test hydroksylacji debryzochiny jako przykład nowych mozliwości badawczych w psychofarmakologii [Debrisoquine hydroxylation test as an example of new possibilities of research in psychopharmacology]. Psychiatr Pol. 1995 Jan-Feb;29(1):57-66. Polish. PMID: 7878155. 8: Saadatmand AR, Tadjerpisheh S, Brockmöller J, Tzvetkov MV. The prototypic pharmacogenetic drug debrisoquine is a substrate of the genetically polymorphic organic cation transporter OCT1. Biochem Pharmacol. 2012 May 15;83(10):1427-34. doi: 10.1016/j.bcp.2012.01.032. Epub 2012 Feb 10. PMID: 22342776. 9: Corado CR, McKemie DS, Knych HK. Dextromethorphan and debrisoquine metabolism and polymorphism of the gene for cytochrome P450 isozyme 2D50 in Thoroughbreds. Am J Vet Res. 2016 Sep;77(9):1029-35. doi: 10.2460/ajvr.77.9.1029. PMID: 27580115. 10: Tucker GT, Silas JH, Iyun AO, Lennard MS, Smith AJ. Polymorphic hydroxylation of debrisoquine. Lancet. 1977 Oct 1;2(8040):718. doi: 10.1016/s0140-6736(77)90527-x. PMID: 71525.