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N-[(7S)-1,2,3,10-tetramethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-7-yl]prop-2-enamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99481-32-0

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99481-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99481-32-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,4,8 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 99481-32:
(7*9)+(6*9)+(5*4)+(4*8)+(3*1)+(2*3)+(1*2)=180
180 % 10 = 0
So 99481-32-0 is a valid CAS Registry Number.

99481-32-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(7S)-1,2,3,10-tetramethoxy-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl]prop-2-enamide

1.2 Other means of identification

Product number -
Other names N-Acryloyldeacetylcolchicine

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:99481-32-0 SDS

99481-32-0Downstream Products

99481-32-0Relevant academic research and scientific papers

Colchicine derivative as well as preparation method and application thereof

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Paragraph 0014; 0039-0041, (2021/06/26)

The invention discloses a colchicine derivative as well as a preparation method and application thereof, and belongs to the technical field of medicines. A low-toxicity colchicine derivative is prepared and then compounded with phospholipid to prepare a phospholipid complex, a sialic acid derivative is adopted to modify the surface of the phospholipid complex to endow the phospholipid complex with targeting property, and the phospholipid complex is used for preparing an anti-tumor safer and more effective colchicine derivative injection. According to the invention, the sialic acid derivative is modified on the surface of the phospholipid complex compounded by the colchicine derivative and the phospholipid, so that the phospholipid complex can be stabilized, and a nano carrier is endowed with neutrophile granulocyte targeting property, so that the colchicine derivative can be used for preparing an active targeting nano dosage form medicine for treating tumors.

N-DIDEUTEROBUTYRYLDEACETYLCOLCHICINE: PROBES TO STUDY COLCHICINE BINDING SITES ON TUBULIN PROTEIN

Iorio, Maria A.,Doldo, Antonio,Brossi, Arnold,Chignell, Colin F.

, p. 2577 - 2581 (2007/10/02)

N-Acryloyl- and N-crotonyldeacetylcolchicine prepared from deacetylcolchiceine by conventional methods showed good binding to tubulin protein in vitro.N-Dideuterobutyryldeacetylcolchicine, prepared from deacetylcolchicine with dideuterobutyryl chloride behaved similarly, suggesting that tritiated analogs of N-propionyl- and N-butyryldeacetylcolchicine should be useful probes to study the colchicine binding site on tubulin protein.

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