MedKoo Cat#: 529159 | Name: Quinelorane hydrochloride

Description:

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

Quinelorane hydrochloride is an antihypertensive.

Chemical Structure

Quinelorane hydrochloride
Quinelorane hydrochloride
CAS#97548-97-5

Theoretical Analysis

MedKoo Cat#: 529159

Name: Quinelorane hydrochloride

CAS#: 97548-97-5

Chemical Formula: C14H24Cl2N4

Exact Mass: 318.1378

Molecular Weight: 319.27

Elemental Analysis: C, 52.67; H, 7.58; Cl, 22.21; N, 17.55

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
Quinelorane hydrochloride
IUPAC/Chemical Name
Pyrido(2,3-g)quinazolin-2-amine, 5,5a,6,7,8,9,9a,10-octahydro-6-propyl-, dihydrochloride, (5aR-trans)-
InChi Key
WDEMLQIGYYLRRX-OWVUFADGSA-N
InChi Code
InChI=1S/C14H22N4.2ClH/c1-2-5-18-6-3-4-10-7-12-11(8-13(10)18)9-16-14(15)17-12;;/h9-10,13H,2-8H2,1H3,(H2,15,16,17);2*1H/t10-,13-;;/m1../s1
SMILES Code
NC1=NC=C2C[C@]3([H])[C@@](CCCN3CCC)([H])CC2=N1.[H]Cl.[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
>3 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
2934.99.03.00
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 319.27 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: Cohen C, Perrault G, Sanger DJ. Preferential involvement of D3 versus D2 dopamine receptors in the effects of dopamine receptor ligands on oral ethanol self-administration in rats. Psychopharmacology (Berl). 1998 Dec;140(4):478-85. PubMed PMID: 9888624. 2: Noh JS, Gwag BJ. Attenuation of oxidative neuronal necrosis by a dopamine D1 agonist in mouse cortical cell cultures. Exp Neurol. 1997 Aug;146(2):604-8. PubMed PMID: 9270075. 3: Thongsaard W, Pongsakorn S, Sudsuang R, Bennett GW, Kendall DA, Marsden CA. Barakol, a natural anxiolytic, inhibits striatal dopamine release but off uptake in vitro. Eur J Pharmacol. 1997 Jan 29;319(2-3):157-64. PubMed PMID: 9042586. 4: Phebus LA, Roush ME, Clemens JA. Effect of direct and indirect dopamine agonists on brain extracellular ascorbate levels in the striatum and nucleus accumbens of awake rats. Life Sci. 1990;47(15):1317-23. PubMed PMID: 1978214.