ChemicalBook--->CAS DataBase List--->14901-16-7

14901-16-7

14901-16-7 Structure

14901-16-7 Structure
IdentificationMore
[Name]

1-PHENYL-3-(2-THIAZOLYL)-2-THIOUREA
[CAS]

14901-16-7
[Synonyms]

1-PHENYL-3-(2-THIAZOLYL)-2-THIOUREA
1-PHENYL-3-(THIAZOL-2-YL)THIOUREA
1-phenyl-3-(2-thiazolyl)-2-thio-ure
n-phenyl-n’-2-thiazolyl-thioure
phenylthiazolylthiourea
1-PHENYL-3-(2-THIAZOLYL)-2-THIOUREA 97&
Urea, 1-phenyl-3-(2-thiazolyl)-2-thio.
1-Phenyl-3-(2-thiazolyl)thiourea
N-Phenyl-N'-(2-thiazolyl)thiourea
N-Phenyl-N'-(thiazol-2-yl)thiourea
U-14624
[EINECS(EC#)]

238-970-4
[Molecular Formula]

C10H9N3S2
[MDL Number]

MFCD00005321
[Molecular Weight]

235.33
[MOL File]

14901-16-7.mol
Chemical PropertiesBack Directory
[Appearance]

light brown fine crystalline powder
[Melting point ]

183-185 °C (dec.)(lit.)
[density ]

1.3479 (rough estimate)
[refractive index ]

1.5500 (estimate)
[form ]

Solid
[color ]

Off-white to yellow
[CAS DataBase Reference]

14901-16-7(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R22:Harmful if swallowed.
R37/38:Irritating to respiratory system and skin .
R41:Risk of serious damage to eyes.
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S39:Wear eye/face protection .
[WGK Germany ]

3
[RTECS ]

YU1398000
Hazard InformationBack Directory
[Chemical Properties]

light brown fine crystalline powder
[Uses]

U-14624 is a potent and orally active dopamine beta-hydroxylase inhibitor. U-14624 suppresses the activities of aminopyrine N-demethylase, aniline hydroxylase and p-nitroanisole O-demethylase enzymes[1][2].
[in vivo]

U-14624 (50 mg/kg; i.p.; daily for 5-7 days) suppresses the activities of aminopyrine N-demethylase, aniline hydroxylase and p-nitroanisole O-demethylase enzymes in rats[2].

Animal Model:150-260 g, Male Sprague-Dawley rats[2]
Dosage:25 mg/kg
Administration:I.p.; daily for 3 days
Result:Prolonged the time required for clearance of pentobarbital from both the plasma and brain, slept significantly longer.
Animal Model:150-260 g, Male Sprague-Dawley rats[2]
Dosage:50 mg/kg
Administration:I.p.; daily for 5-7 days
Result:Suppressed the activities of aminopyrine N-demethylase, aniline hydroxylase and p-nitroanisole O-demethylase enzymes.
[References]

[1] Von Voigtlander PF, et al. Behavioral and brain catecholamine depleting actions of U-14,624, an inhibitor of dopamine beta-hydroxylase. Proc Soc Exp Biol Med. 1970 Mar;133(3):817-20. DOI:10.3181/00379727-133-34571
[2] Smith JR, et al. Effect of the catecholamine-depleting agent 1-phenyl-3-(2-thiazolyl)-2-thiourea (U-14,624) on drug metabolism in the rat. Biochem Pharmacol. 1980 Sep 15;29(18):2425-30. DOI:10.1016/0006-2952(80)90345-7
Spectrum DetailBack Directory
[Spectrum Detail]

1-PHENYL-3-(2-THIAZOLYL)-2-THIOUREA(14901-16-7)MS
1-PHENYL-3-(2-THIAZOLYL)-2-THIOUREA(14901-16-7)1HNMR
1-PHENYL-3-(2-THIAZOLYL)-2-THIOUREA(14901-16-7)13CNMR
1-PHENYL-3-(2-THIAZOLYL)-2-THIOUREA(14901-16-7)IR1
1-PHENYL-3-(2-THIAZOLYL)-2-THIOUREA(14901-16-7)IR2
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

14901-16-7(sigmaaldrich)
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