Amoxicillin
Amoxicillin is a penicillin in which the substituent at position 6 of the penam ring is a 2-amino-2-(4-hydroxyphenyl)acetamido group. It has a role as an antibacterial drug
General
Type : Antibiotic, Azabicyclo
Chemical_Nomenclature : (2S,5R,6R)-6-[[(2R)-2-amino-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
Canonical SMILES : CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=C(C=C3)O)N)C(=O)O)C
InChI : InChI=1S\/C16H19N3O5S\/c1-16(2)11(15(23)24)19-13(22)10(14(19)25-16)18-12(21)9(17)7-3-5-8(20)6-4-7\/h3-6,9-11,14,20H,17H2,1-2H3,(H,18,21)(H,23,24)\/t9-,10-,11+,14-\/m1\/s1
InChIKey : LSQZJLSUYDQPKJ-NJBDSQKTSA-N
Other name(s) : Amoxycillin || CHEBI:2676 || CHEMBL1082 || CHEBI:53712 || ZINC3830215 || DB01060
MW : 365.4
Formula : C16H19N3O5S
CAS_number : 26787-78-0
PubChem : 33613
UniChem : LSQZJLSUYDQPKJ-NJBDSQKTSA-N
Wikipedia : Amoxicillin
Target
Structures : No structure
Families : Carb_B_Chordata
References (1)
| Title : Pig liver esterases PLE1 and PLE6: heterologous expression, hydrolysis of common antibiotics and pharmacological consequences - Zhou_2019_Sci.Rep_9_15564 |
| Author(s) : Zhou Q , Xiao Q , Zhang Y , Wang X , Xiao Y , Shi D |
| Ref : Sci Rep , 9 :15564 , 2019 |
| Abstract : |
| PubMedSearch : Zhou_2019_Sci.Rep_9_15564 |
| PubMedID: 31664043 |
| Gene_locus related to this paper: pig-EST1 , pig-a0a1s6l967 |