Cardiovascular effects of new water-soluble derivatives of forskolin

DOI: 10.1021/jm00118a002

Source and publish data:

Journal of Medicinal Chemistry p. 1872 - 1879 (1988)

Update date:2022-08-05

Topics:

Authors:

Khandelwal

Rajeshwari

Rajagopalan

Swamy Swamy

Dohadwalla

De Souza

Rupp Rupp

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

Article abstract of DOI:10.1021/jm00118a002

A series of 6- and 7-aminoacyl derivatives of 7-deacetylforskolin was prepared to provide water-soluble derivatives of the potent cardioactive diterpenoid forskolin. The compounds were evaluated for positive inotropic and blood pressure lowering propertie

Full text of DOI:10.1021/jm00118a002

Products guided by the article

Product name:2-Phenylamino-propionic acid (3R,4aR,5S,6S,6aS,10S,10aR,10bS)-6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-3-vinyl-dodecahydro-benzo[f]chromen-5-yl ester

Cas No:115076-71-6

R&D Labs maybe for 115076-71-6

Nantong Auxin Electronic Technology Co., LTD

Contact:86-513-88760026

Address:NO.5-1, Aoxin Road, Haian Hi-tech Development Zone, Jiangsu Province, China
Chengdu Aslee Biopharmaceuticals, Inc

Contact:18608018419

Address:Chengdu Aslee Biopharmaceuticals, Inc
Chengdu Pukang Biotechnology Co., Ltd

Contact:+86-28-82550498

Address:No. 558 Rulin Road,Xinjin county,Chengdu city, China
Beijing Pure Chem Co.,Ltd.

Contact:+86-10-83993285

Address:Rm.1708, Haobai Tower, Building 6, No.50, North Road, West Third Ring, Haidian District, Beijing, China
Tianjin Chemsyntech Chemical Co., Ltd

Contact:+86-22-60872258

Address:Haitai green industry base in Tianjin, K1,5-601

Relevant to this article

HIGHLY STEREOSELECTIVE REDUCTION OF CHIRAL α-KETO-β,γ-UNSATURATED ACETALS: SYNTHESIS OF BOTH EPIMERIC ALLYL ALCOHOLS BY PROPER CHOICE OF ADDITIVE

Doi:10.1016/S0040-4039(00)96812-6
(1987)
Synthesis of D/L-erythro-Sphingosine Using a Tethered Aminohydroxylation Reaction as the Key Step

Doi:10.1055/s-0028-1083367
(2009)
One-pot regioselective synthesis of 1,4,5-trisubstituted pyrazoles under solvent-free conditions without catalyst

Doi:10.1007/s00706-012-0721-9
(2012)
Rongalite and base-promoted cleavage of disulfides and subsequent Michael addition to α,β-unsaturated ketones/esters: an odorless synthesis of β-sulfido carbonyl compounds

Doi:10.1016/j.tet.2010.02.001
(2010)
Highly chemoselective synthesis of 6-Alkoxy-l-aIkyl(aryl)-3- trifluoroaeetyl-1,4,5,6 tetrahydropyridlines and 1-Alkyl(aryl)-6-anino-3- trifluoroacetyl-1,4,5,6-tetrahydropyridines

Doi:10.1002/ejoc.200801119
(2009)
Renin inhibitors containing hydrophilic groups. Tetrapeptides with enhanced aqueous solubility and nanomolar potency

Doi:10.1021/jm00118a009
(1988)

Article Doi