Welcome to LookChem.com Sign In|Join Free
  • or
Esperamicin A1 is a naturally occurring antibiotic and antitumor agent isolated from Actinomadura verrucosopora. Its chemical structure consists of a core bicyclo[7.3.1]tridecadiynene moiety containing a 1,5-diyn-3-ene as part of a ten-membered ring, an alpha,beta-unsaturated ketone with a bridgehead double bond, and an attached allylic trisulfide. This ring system is attached at one end by a trisaccharide moiety and at the opposite end by a 2-deoxy-L-fucose-anthrailate moiety. The trisaccharide consists of a hydroxyamino sugar connected to an isopropylamino sugar through a glycosidic linkage and a thiomethyl sugar through an NH1O linkage.

99674-26-7

Post Buying Request

99674-26-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

99674-26-7 Usage

Uses

Used in Pharmaceutical Industry:
Esperamicin A1 is used as an antibiotic and antitumor agent for its ability to inhibit the growth of certain bacteria and tumor cells. Its unique chemical structure allows it to target specific cellular processes, making it a promising candidate for the development of new drugs to treat bacterial infections and cancer.
Used in Cancer Research:
Esperamicin A1 is used as a research tool for studying the mechanisms of action of antibiotics and antitumor agents. Its complex chemical structure provides insights into the development of new drugs with improved efficacy and reduced side effects.
Used in Drug Development:
Esperamicin A1 is used as a lead compound in the development of new drugs with antibiotic and antitumor properties. Its unique structure and activity can be used as a starting point for the design and synthesis of new compounds with improved pharmacological properties.
Used in Drug Delivery Systems:
Esperamicin A1 can be used in drug delivery systems to improve the bioavailability and therapeutic efficacy of the compound. Novel drug delivery systems, such as nanoparticles or liposomes, can be developed to encapsulate and protect esperamicin A1, allowing for controlled release and targeted delivery to specific tissues or cells.

Check Digit Verification of cas no

The CAS Registry Mumber 99674-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,6,7 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 99674-26:
(7*9)+(6*9)+(5*6)+(4*7)+(3*4)+(2*2)+(1*6)=197
197 % 10 = 7
So 99674-26-7 is a valid CAS Registry Number.
InChI:InChI=1/C59H80N4O22S4/c1-28(2)60-36-27-77-43(25-39(36)73-8)83-52-50(66)47(63-85-45-24-37(64)53(86-12)31(5)79-45)29(3)80-57(52)82-38-18-16-14-15-17-20-59(71)34(19-21-88-89-87-13)46(38)48(62-58(70)76-11)51(67)54(59)84-44-26-42(49(65)30(4)78-44)81-56(69)33-22-40(74-9)41(75-10)23-35(33)61-55(68)32(6)72-7/h14-15,19,22-23,28-31,36-39,42-45,47,49-50,52-54,57,60,63-66,71H,6,21,24-27H2,1-5,7-13H3,(H,61,68)(H,62,70)/b15-14-,34-19+

99674-26-7SDS

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 esperamicin A1

1.2 Other means of identification

Product number -
Other names -

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:99674-26-7 SDS

99674-26-7Upstream product

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 99674-26-7