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ANTIMYCIN A2, a homologue of the antimycin complex, is a potent inhibitor of respiration that was first resolved from antimycin A1 in 1959. It is known for its ability to inhibit the oxidation of ubiquinol to ubiquinone, thereby exhibiting broad biological activity. ANTIMYCIN A2 possesses antifungal, anthelmintic, insecticidal, antiviral, and antitumor properties, making it a versatile compound with potential applications in various industries.

27220-57-1

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27220-57-1 Usage

Uses

Used in Pharmaceutical Industry:
ANTIMYCIN A2 is used as an antifungal agent for treating fungal infections due to its ability to inhibit fungal respiration and growth.
ANTIMYCIN A2 is used as an anthelmintic agent for combating parasitic worm infections, as it can effectively target and inhibit the respiration of these parasites.
ANTIMYCIN A2 is used as an insecticide for controlling insect populations, leveraging its potent inhibitory effects on insect respiration.
ANTIMYCIN A2 is used as an antiviral agent for inhibiting viral replication and reducing the spread of viral infections.
ANTIMYCIN A2 is used as an antitumor agent for its potential in targeting and inhibiting the respiration of cancer cells, thereby exhibiting antitumor activity.
Used in Agricultural Industry:
ANTIMYCIN A2 is used as an insecticide for protecting crops from insect damage, contributing to increased crop yield and reduced economic losses due to pest infestations.
Used in Environmental Management:
ANTIMYCIN A2 can be used in the control of harmful algal blooms, as its antifungal properties may also be effective against certain types of algae that can cause environmental issues.
Used in Research and Development:
ANTIMYCIN A2 serves as a valuable tool in scientific research, particularly in the study of cellular respiration, oxidative phosphorylation, and the development of new drugs targeting these processes. Its unique molecular targets and broad biological activity make it an important compound for understanding various biological pathways and developing novel therapeutic strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 27220-57-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,2,2 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27220-57:
(7*2)+(6*7)+(5*2)+(4*2)+(3*0)+(2*5)+(1*7)=91
91 % 10 = 1
So 27220-57-1 is a valid CAS Registry Number.
InChI:InChI=1/C27H38N2O9/c1-5-7-8-9-12-19-24(38-21(31)11-6-2)17(4)37-27(35)22(16(3)36-26(19)34)29-25(33)18-13-10-14-20(23(18)32)28-15-30/h10,13-17,19,22,24,32H,5-9,11-12H2,1-4H3,(H,28,30)(H,29,33)

27220-57-1SDS

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-[(3-formamido-2-hydroxybenzoyl)amino]-8-hexyl-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl] butanoate

1.2 Other means of identification

Product number -
Other names EINECS 248-342-1

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:27220-57-1 SDS

27220-57-1Upstream product

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