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65490-24-6

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  • ANHYDROCHLORTETRACYCLINE HYDROCHLORIDE, CAN BE USED AS SECONDARY STANDARD

    Cas No: 65490-24-6

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65490-24-6 Usage

Chemical Properties

orange to red-brown crystalline powder

Uses

Anhydrochlortetracycline is the anhydro analogue and impurity of Chlortetracycline (C426500). Anhydrochlortetracycline is an antimicrobial and antibacterial.

Check Digit Verification of cas no

The CAS Registry Mumber 65490-24-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,9 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65490-24:
(7*6)+(6*5)+(5*4)+(4*9)+(3*0)+(2*2)+(1*4)=136
136 % 10 = 6
So 65490-24-6 is a valid CAS Registry Number.

65490-24-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5a,6-anhydrochlorotetracycline hydrochloride

1.2 Other means of identification

Product number -
Other names ANHYDROCHLORTETRACYCLINE HYDROCHLORIDE

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:65490-24-6 SDS

65490-24-6Downstream Products

65490-24-6Relevant articles and documents

Semisynthetic analogues of anhydrotetracycline as inhibitors of tetracycline destructase enzymes

Markley, Jana L.,Fang, Luting,Gasparrini, Andrew J.,Symister, Chanez T.,Kumar, Hirdesh,Tolia, Niraj H.,Dantas, Gautam,Wencewicz, Timothy A.

, p. 618 - 633 (2019/03/19)

The synthesis and biological evaluation of semisynthetic anhydrotetracycline analogues as small molecule inhibitors of tetracycline-inactivating enzymes are reported. Inhibitor potency was found to vary as a function of enzyme (major) and substrate-inhibitor pair (minor), and anhydrotetracycline analogue stability to enzymatic and nonenzymatic degradation in solution contributes to their ability to rescue tetracycline activity in whole cell Escherichia coli expressing tetracycline destructase enzymes. Taken collectively, these results provide the framework for the rational design of next-generation inhibitor libraries en route to a viable and proactive adjuvant approach to combat the enzymatic degradation of tetracycline antibiotics.

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