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175795-76-3

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  • 5,12-Naphthacenedione,7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(2-hydroxyacetyl)-1-methoxy-10-[[2,3,6-trideoxy-3-(2,3-dihydro-1H-pyrrol-1-yl)-a-L-lyxo-hexopyranosyl]oxy]-, (8S,10S)-

    Cas No: 175795-76-3

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175795-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 175795-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,7,9 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 175795-76:
(8*1)+(7*7)+(6*5)+(5*7)+(4*9)+(3*5)+(2*7)+(1*6)=193
193 % 10 = 3
So 175795-76-3 is a valid CAS Registry Number.
InChI:InChI=1/C31H33NO11/c1-14-26(35)17(32-8-3-4-9-32)10-21(42-14)43-19-12-31(40,20(34)13-33)11-16-23(19)30(39)25-24(28(16)37)27(36)15-6-5-7-18(41-2)22(15)29(25)38/h3,5-8,14,17,19,21,26,33,35,37,39-40H,4,9-13H2,1-2H3/t14-,17-,19-,21-,26+,31-/m0/s1

175795-76-3SDS

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 AN 201

1.2 Other means of identification

Product number -
Other names 2-pyrollinodoxorubicin

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:175795-76-3 SDS

175795-76-3Downstream Products

175795-76-3Relevant articles and documents

Aldolase antibody activation of prodrugs of potent aldehyde-containing cytotoxics for selective chemotherapy

Sinha, Subhash C.,Li, Lian-Sheng,Watanabe, Shin-Ichi,Kaltgrad, Eiton,Tanaka, Fujie,Rader, Christoph,Lerner, Richard A.,Barbas III, Carlos F.

, p. 5467 - 5472 (2004)

Prodrugs of potent aldehyde analogues of the anticancer drug doxorubicin (Dox) were synthesized. These prodrugs were efficiently activated by antibody 93F3 and no drug formation was observed in the absence of 93F3 in either phosphate buffered saline or cell culture media. In the presence of antibody 93F3, these prodrugs were activated and decreased the proliferation of human cancer cells in in vitro proliferation assays.

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