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Hippeastrine, an indole alkaloid, is a naturally occurring compound that can be isolated from the Amaryllidaceae family. It has been demonstrated to possess cytotoxic properties, making it a potential candidate for various pharmaceutical and industrial applications.

477-17-8

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477-17-8 Usage

Uses

Used in Pharmaceutical Applications:
Hippeastrine is used as a cytotoxic agent for its ability to inhibit the growth and proliferation of cancer cells. This characteristic makes it a valuable compound in the development of anticancer drugs and therapies.
Used in Chemical Research:
As a naturally occurring indole alkaloid, hippeastrine is also utilized in chemical research to study its structure, properties, and potential interactions with other compounds. This research can lead to the discovery of new applications and uses for hippeastrine in various industries.
Used in Drug Delivery Systems:
Similar to gallotannin, hippeastrine can be incorporated into drug delivery systems to enhance its bioavailability and therapeutic outcomes. By using carriers such as organic and metallic nanoparticles, the limitations of hippeastrine can be overcome, improving its delivery and efficacy against target cells or tissues.

Check Digit Verification of cas no

The CAS Registry Mumber 477-17-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 477-17:
(5*4)+(4*7)+(3*7)+(2*1)+(1*7)=78
78 % 10 = 8
So 477-17-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H17NO5/c1-18-3-2-8-4-11(19)16-14(15(8)18)9-5-12-13(22-7-21-12)6-10(9)17(20)23-16/h4-6,11,14-16,19H,2-3,7H2,1H3/t11-,14-,15+,16+/m0/s1

477-17-8SDS

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 hippeastrine

1.2 Other means of identification

Product number -
Other names Hippeastrine

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:477-17-8 SDS

477-17-8Relevant academic research and scientific papers

SYNTHESIS OF AN AMARYLLIDACEAE ALKALOID, (+/-)-HIPPEASTRINE

Katakawa, Jun'ichi,Merugi, Haruo,Irie, Hiroshi

, p. 2213 - 2216 (2007/10/02)

Total synthesis of one of Amaryllidaceae alkaloids, hippeastrine, was accomplished starting from methyl 2c-(N-methoxycarbonylamino)-3t-(3,4-methylenedioxyphenyl)cyclohex-4-enyl-r-acetate in stereoselective manner.

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