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58189-27-8

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  • methyl (1R,2S,4aR,4bS,7E,8R,8aS,9R,10aR)-2,9-dihydroxy-1,4a,8-trimethyl-7-(2-methylaminoethoxycarbonylmethylidene)-10-oxo-2,3,4,4b,5,6,8,8a,9,10a-decahydrophenanthrene-1-carboxylate

    Cas No: 58189-27-8

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  • methyl (1R,2S,4aR,4bS,7E,8R,8aS,9R,10aR)-2,9-dihydroxy-1,4a,8-trimethyl-7-(2-methylaminoethoxycarbonylmethylidene)-10-oxo-2,3,4,4b,5,6,8,8a,9,10a-decahydrophenanthrene-1-carboxylate cas 58189-27-8

    Cas No: 58189-27-8

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58189-27-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58189-27-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,8 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58189-27:
(7*5)+(6*8)+(5*1)+(4*8)+(3*9)+(2*2)+(1*7)=158
158 % 10 = 8
So 58189-27-8 is a valid CAS Registry Number.

58189-27-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Hydroxynorerythrosuamide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:58189-27-8 SDS

58189-27-8Upstream product

58189-27-8Downstream Products

58189-27-8Relevant articles and documents

Chemical and pharmacological characterization of Erythrophleum lasianthum alkaloids

Verotta,Aburjai,Rogers,Dorigo,Maragno,Fraccarollo,Santostasi,Gaion,Floreani,Carpenedo

, p. 271 - 274 (1995)

Two alkaloids 1 and 2 were isolated from the seeds of Erythrophleum lasianthum. Their structures were assigned by spectroscopic and chemical means as 3β-hydroxynorerythrosuamine (1) and its 3-O-β-D-glucopyranoside (2). In spontaneously beating atria, both compounds 1 and 2 showed a marked and concentration-dependent positive inotropic activity and a weak negative chronotropic activity. The positive inotropic effect induced by 1 and 2 was not modified by propranolol, prazosin, carbachol, and ranitidine plus pyrilamine. Both 1 and 2 were very active in inhibiting the Na+/K+-ATPase isolated from bovine cardiac sarcolemmal vesicles.

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