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Details

Stereochemistry ABSOLUTE
Molecular Formula C47H70O14
Molecular Weight 859.0503
Optical Activity UNSPECIFIED
Defined Stereocenters 19 / 19
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ABAMECTIN B1B

SMILES

[H][C@@]12OC\C3=C/C=C/[C@H](C)[C@H](O[C@@]4([H])C[C@H](OC)[C@@]([H])(O[C@@]5([H])C[C@H](OC)[C@@H](O)[C@H](C)O5)[C@H](C)O4)\C(C)=C\C[C@]6([H])C[C@@H](C[C@]7(O6)O[C@]([H])(C(C)C)[C@@H](C)C=C7)OC(=O)[C@]([H])(C=C(C)[C@H]1O)[C@@]23O

InChI

InChIKey=ZFUKERYTFURFGA-PVVXTEPVSA-N
InChI=1S/C47H70O14/c1-24(2)41-27(5)16-17-46(61-41)22-33-19-32(60-46)15-14-26(4)42(25(3)12-11-13-31-23-54-44-39(48)28(6)18-34(45(50)57-33)47(31,44)51)58-38-21-36(53-10)43(30(8)56-38)59-37-20-35(52-9)40(49)29(7)55-37/h11-14,16-18,24-25,27,29-30,32-44,48-49,51H,15,19-23H2,1-10H3/b12-11+,26-14+,31-13+/t25-,27-,29-,30-,32+,33-,34-,35-,36-,37-,38-,39+,40-,41+,42-,43-,44+,46+,47+/m0/s1

HIDE SMILES / InChI
Abamectin B1b (Avermectin B1b) is a macrocyclic lactone containing an isopropyl reside in the 25-position broad anthelmintic activity. The oral administration of this formulation of avermectin B1 appeared to be highly efficacious against intestinal strongyles and Onchocera microfilaria. Avermectin B1b is a component of marketed and provided commercially Abamectin, which is used to control livestock parasitic nematodes. It is a broad-spectrum acaricide with additional insecticidal action on a limited number of insects. Abamectin acts on insects by increasing the membrane permeability to chloride ions, and it mainly stimulates the release of Ȗ-aminobutyric acid (GABA). The affected arthropod becomes paralysed, stops feeding, and dies after a few days. It exerts contact and stomach action, with limited plant systemic activity, but exhibits translaminar movement into treated leaves. Abamectin is also used as an anthelmintic drug in veterinary medicine.

Approval Year

PubMed

PubMed

TitleDatePubMed
Determination of abamectin in citrus fruits using SPE combined with dispersive liquid-liquid microextraction and HPLC-UV detection.
2013 Aug
Antiviral effect of theaflavins against caliciviruses.
2017 Apr
Patents

Sample Use Guides

Horses: avermectin B1 solution (0.2 mg/kg p.o.). The avermectin B1 was a 1% solution in a propylene glycolglycerol formal base.
Route of Administration: Oral
Name Type Language
ABAMECTIN B1B
Common Name English
AVERMECTIN B1B
Common Name English
ABAMECTIN COMPONENT B1B
Common Name English
AVERMECTIN A1A, 5-O-DEMETHYL-25-DE(1-METHYLPROPYL)-25-(1-METHYLETHYL)-
Common Name English
IVERMECTIN IMPURITY B [EP IMPURITY]
Common Name English
Code System Code Type Description
SMS_ID
300000024013
Created by admin on Fri Dec 15 17:25:32 GMT 2023 , Edited by admin on Fri Dec 15 17:25:32 GMT 2023
PRIMARY
ECHA (EC/EINECS)
265-611-9
Created by admin on Fri Dec 15 17:25:32 GMT 2023 , Edited by admin on Fri Dec 15 17:25:32 GMT 2023
PRIMARY
CAS
65195-56-4
Created by admin on Fri Dec 15 17:25:32 GMT 2023 , Edited by admin on Fri Dec 15 17:25:32 GMT 2023
PRIMARY
FDA UNII
W8DT67027W
Created by admin on Fri Dec 15 17:25:32 GMT 2023 , Edited by admin on Fri Dec 15 17:25:32 GMT 2023
PRIMARY
EPA CompTox
DTXSID4058239
Created by admin on Fri Dec 15 17:25:32 GMT 2023 , Edited by admin on Fri Dec 15 17:25:32 GMT 2023
PRIMARY
ChEMBL
CHEMBL2079552
Created by admin on Fri Dec 15 17:25:32 GMT 2023 , Edited by admin on Fri Dec 15 17:25:32 GMT 2023
PRIMARY
PUBCHEM
6858005
Created by admin on Fri Dec 15 17:25:32 GMT 2023 , Edited by admin on Fri Dec 15 17:25:32 GMT 2023
PRIMARY
CHEBI
29537
Created by admin on Fri Dec 15 17:25:32 GMT 2023 , Edited by admin on Fri Dec 15 17:25:32 GMT 2023
PRIMARY