Trequinsin hydrochloride

Modify Date: 2025-08-20 20:18:00

Trequinsin hydrochloride Structure
Trequinsin hydrochloride structure
Common Name Trequinsin hydrochloride
CAS Number 78416-81-6 Molecular Weight 441.95000
Density N/A Boiling Point 613.8ºC at 760 mmHg
Molecular Formula C24H28ClN3O3 Melting Point N/A
MSDS USA Flash Point 325ºC

 Use of Trequinsin hydrochloride


Trequinsin hydrochloride (HL 725) is an extremely potent inhibitor of platelet CAMP phosphodiesterase (PDE), with an IC50 of 0.25 nM. Trequinsin hydrochloride (HL 725) is an extremely potent inhibitor of the aggregation of human platelets induced in vitro by ADP, collagen, thrombin and epinephrine[1][2][3].

 Names

Name Trequinsin hydrochloride,2,3,6,7-Tetrahydro-9,10-dimethoxy-3-methyl-2-[(2,4,6-trimethylphenyl)imino]-4H-pyrimido[6,1-a]isoquinolin-4-onehydrochloride
Synonym More Synonyms

 Trequinsin hydrochloride Biological Activity

Description Trequinsin hydrochloride (HL 725) is an extremely potent inhibitor of platelet CAMP phosphodiesterase (PDE), with an IC50 of 0.25 nM. Trequinsin hydrochloride (HL 725) is an extremely potent inhibitor of the aggregation of human platelets induced in vitro by ADP, collagen, thrombin and epinephrine[1][2][3].
Related Catalog
In Vitro Trequinsin hydrochloride exerts besides its cardiovascular and antihypertensive qualities very potent antiplatelet activities[1]. Trequinsin hydrochloride is an efficacious agonist of [Ca2+]i[3]. Cell Viability Assay[3] Cell Line: Samples from healthy volunteer research donors with normal sperm motility parameters in agreement with World Health Organization 2010 criteria. Concentration: 10 μM. Incubation Time: 20 min. Result: Caused a concentrationdependent increase in [Ca2+]i (EC50 = 6.4 μM [95% confidence interval (CI): 4.1-9.9 μM]).
References

[1]. D Ruppert,, et al. HL 725, an extremely potent inhibitor of platelet phosphodiesterase and induced platelet aggregation in vitro. Life Sci. 1982 Nov 8;31(19):2037-43.

[2]. K C Agarwal, et al. Role of plasma adenosine in the antiplatelet action of HL 725, a potent inhibitor of cAMP phosphodiesterase: species differences. Thromb Res. 1987 Jul 15;47(2):191-200.

[3]. Rachel C McBrinn, et al. Novel pharmacological actions of trequinsin hydrochloride improve human sperm cell motility and function. Br J Pharmacol. 2019 Dec;176(23):4521-4536.

 Chemical & Physical Properties

Boiling Point 613.8ºC at 760 mmHg
Molecular Formula C24H28ClN3O3
Molecular Weight 441.95000
Flash Point 325ºC
Exact Mass 441.18200
PSA 57.75000
LogP 4.38670

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
UW7727000
CHEMICAL NAME :
4H-Pyrimido(6,1-a)isoquinolin-4-one, 2,3,6,7-tetrahydro-9,10-dimethoxy-3-methyl- 2-((2,4,6-trimethylphenyl)imino)-, monohydrochloride
CAS REGISTRY NUMBER :
78416-81-6
LAST UPDATED :
198803
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C24-H27-N3-O3.Cl-H
MOLECULAR WEIGHT :
442.00

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
150 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JMCMAR Journal of Medicinal Chemistry. (American Chemical Soc., Distribution Office Dept. 223, POB POB 57136, West End Stn., Washington, DC 20037) V.6- 1963- Volume(issue)/page/year: 27,1470,1984

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
RIDADR NONH for all modes of transport
WGK Germany 3
RTECS UW7727000

 Articles28

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 Synonyms

trequinsine
HL 725 HCL
TREQUINSIN HYDROCHLORIDE MINIMUM
TREQUINSIN HYDROCHLORIDE
Trequinsin,HCl
HL 725
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