Terazocin Hydrochloride (anhydrous)

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

MedKoo CAT#: 571341

CAS#: 63074-08-8

Description: Terazocin Hydrochloride is a potent and selective α1-adrenergic receptor that may induce decreased blood pressure and is used in the treatment of benign prostatic hyperplasia.


Chemical Structure

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Terazocin Hydrochloride (anhydrous)
CAS# 63074-08-8

Theoretical Analysis

MedKoo Cat#: 571341
Name: Terazocin Hydrochloride (anhydrous)
CAS#: 63074-08-8
Chemical Formula: C19H26ClN5O4
Exact Mass: 423.17
Molecular Weight: 423.900
Elemental Analysis: C, 53.84; H, 6.18; Cl, 8.36; N, 16.52; O, 15.10

Price and Availability

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100mg USD 240
250mg USD 500
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Synonym: Terazocin HCl; Vasocard; Hyprin; A-45975; A 45975; A45975

IUPAC/Chemical Name: Piperazine, 1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-((tetrahydro-2-furanyl)carbonyl)-, monohydrochloride

InChi Key: IWSWDOUXSCRCKW-UHFFFAOYSA-N

InChi Code: InChI=1S/C19H25N5O4.ClH/c1-26-15-10-12-13(11-16(15)27-2)21-19(22-17(12)20)24-7-5-23(6-8-24)18(25)14-4-3-9-28-14;/h10-11,14H,3-9H2,1-2H3,(H2,20,21,22);1H

SMILES Code: O=C(N1CCN(C2=NC(N)=C3C=C(OC)C(OC)=CC3=N2)CC1)C4OCCC4.[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: >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:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 423.90 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
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1: An GH, Kim MJ, Lee HJ, Park SS, Cho YW, Park K, Choa YH. Fabrication of terazocin-loaded poly(D,L-lactide) microspheres by an ultrasonic spray drying method and their release behaviors. J Nanosci Nanotechnol. 2008 Oct;8(10):5139-42. PubMed PMID: 19198407.

2: Liu G. [Effects of terazocin on hypertensive patients]. Zhonghua Xin Xue Guan Bing Za Zhi. 1990 Oct;18(5):271-2. Chinese. PubMed PMID: 1982259.

3: Kotridis P, Kokkas B, Kyriakou P, Karamouzis M, Salpigidis G, Karantona C, Karadoumanis J, Ginis T, Goulis O, Papadopoulos PC, Vakalopoulos C, Sakantamis G, Dimitriadou A, Mirtsou-Fidani V, Papadopoulos CL. Plasma atrial natriuretic peptide in essential hypertension after treatment with terazocin. Eur J Drug Metab Pharmacokinet. 2003 Apr-Jun;28(2):143-6. PubMed PMID: 12877573.

4: Pawar A, Fahim M. Baroreceptor mediated blood pressure regulation is not affected during dose dependent inhibition of prostatic contractions by terazosin. Indian J Physiol Pharmacol. 2004 Oct;48(4):419-27. PubMed PMID: 15907050.