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Indoramin

Names

[ CAS No. ]:
26844-12-2

[ Name ]:
Indoramin

[Synonym ]:
3-<2-(4-Benzamidopiperid-1-yl)ethyl>indol
Indoramine [INN-French]
N-[1-(2-indol-3-yl-ethyl)-piperidin-4-yl]-benzamide
3-[2-(4-benzamido-1-piperidyl)ethyl]indole
INDORAMIN
Indoramine
3-[2-(4-benzamidopiperid-1-yl)ethyl]indole
Indoramina [INN-Spanish]
EINECS 248-041-5
Benzamide,N-(1-(2-(1H-indol-3-yl)ethyl)-4-piperidinyl)
Indoraminum [INN-Latin]

Biological Activity

[Description]:

Indoramin is an orally active antihypertensive agent. Indoramin is also selective for the α1A-adrenoceptor[1].

[Related Catalog]:

Research Areas >> Endocrinology
Signaling Pathways >> GPCR/G Protein >> Adrenergic Receptor

[References]

[1]. M Eltze, et al. In functional experiments, risperidone is selective, not for the B, but for the A subtype of alpha 1-adrenoceptors. Eur J Pharmacol. 1996 Jan 4;295(1):69-73.

Chemical & Physical Properties

[ Density]:
1.21g/cm3

[ Boiling Point ]:
600ºC at 760mmHg

[ Melting Point ]:
208-210°

[ Molecular Formula ]:
C22H25N3O

[ Molecular Weight ]:
347.45300

[ Flash Point ]:
316.7ºC

[ Exact Mass ]:
347.20000

[ PSA ]:
48.13000

[ LogP ]:
3.93360

[ Vapour Pressure ]:
2.36E-14mmHg at 25°C

[ Index of Refraction ]:
1.657

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
CV5395900
CHEMICAL NAME :
Benzamide, N-(1-(2-(1H-indol-3-yl)ethyl)-4-piperidinyl)-
CAS REGISTRY NUMBER :
26844-12-2
BEILSTEIN REFERENCE NO. :
0494035
LAST UPDATED :
199612
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C22-H25-N3-O
MOLECULAR WEIGHT :
347.50

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1800 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: 14,1054,1971
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
500 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: 14,1054,1971
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>400 mg/kg
TOXIC EFFECTS :
Vascular - BP lowering not characterized in autonomic section
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: 14,1054,1971

Safety Information

[ HS Code ]:
2933990090

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Related Compounds

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