Synthesis and hypotensive activities of octahydropyrazinopyridoindoles and 15-azayohimbanes

DOI: 10.1016/0223-5234(94)90114-7

Source and publish data:

European Journal of Medicinal Chemistry p. 899 - 902 (1994)

Update date:2022-08-04

Topics:

Authors:

Valls, N.

Segarra, V. M.

Tost, A.

Rosell, G.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/0223-5234(94)90114-7

The hypotensive activities in rats of indolic compounds 1-9 were compared with that of reserpine.In spite of differences in their structure, all 9 showed similar hypotensive activities to that of reserpine.New octahydropyrazinopyridoindoles 3-6 and the te

Full text of DOI:10.1016/0223-5234(94)90114-7

Products guided by the article

Product name:2-cyclohexylmethyl-1,2,3,4,6,7,12,12b-octahydropyrazino<1',2':1,2>pyrido<3,4-b>indole

Cas No:137606-60-1

R&D Labs maybe for 137606-60-1

Xinchang Yueding Chemical Co., Ltd.

Contact:86-571-56926323

Address:NO.90 BEIMENCHENGWAI CHENGGUAN TOWN XINCHANG
Hangzhou utanpharma Co., Ltd

Contact:86-571-87758773

Address:Room604 ,6F, Block A1-3 Xixi Plaza,No. 588 Wenyi West RD, Hangzhou,310012, China
Hubei ShiNan Pharmaceutical Chemical co., Ltd.(expird)

Contact:+86-13554447107

Address:Wuhan HongShanOu wu no road 378 future residence building 1 unit 14 layer no. 1401 A
PharmOrgsyn

Contact:+86-21-38228826

Address:Room 505 Building 2, No 3377 Kangxin Highway, Shanghai, Republic China

Relevant to this article

Samarium(II) iodide promoted radical ring opening reactions of cyclopropyl ketones

Doi:10.1016/0040-4039(91)80791-4
(1991)
First total synthesis of A₂ isoprostane

Doi:10.1021/jo025652f
(2002)
Efficient luminescence from a copper(i) complex doped in organic light-emitting diodes by suppressing C-H vibrational quenching

Doi:10.1039/c2cc31509b
(2012)
N-heterocyclic carbene-catalyzed cyclization of unsaturated acyl chlorides and ketones

Doi:10.1002/adsc.201100178
(2011)
Nucleophilic openings of bicyclic β-lactones via acyl C-O and alkyl C-O cleavage: Catalytic, asymmetric synthesis of a versatile, carbocyclic nucleoside precursor and protected transpentacin

Doi:10.1016/S0040-4020(02)00703-2
(2002)
Preparation of chiral 3-arylpyrrolidines via the enantioselective 1,4-addition of arylboronic acids to fumaric esters catalyzed by Rh(I)/chiral diene complexes

Doi:10.1021/ol300980k
(2012)

Article Doi