CHEBI:75262 - pipacycline

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name pipacycline
Definition Tetracycline in which a hydrogen attached to the amide nitrogen is substituted by a 4-[(2-hydroxyethyl)piperazin-1-yl]methyl group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C29H38N4O9
Net Charge 0
Average Mass 586.63340
Monoisotopic Mass 586.26388
InChI InChI=1S/C29H38N4O9/c1-28(41)15-5-4-6-18(35)19(15)23(36)20-16(28)13-17-22(31(2)3)24(37)21(26(39)29(17,42)25(20)38)27(40)30-14-33-9-7-32(8-10-33)11-12-34/h4-6,16-17,22,34-35,37-38,41-42H,7-14H2,1-3H3,(H,30,40)/t16-,17-,22-,28+,29-/m0/s1
SMILES [H][C@@]12C[C@@]3([H])C(C(=O)c4c(O)cccc4[C@@]3(C)O)=C(O)[C@]1(O)C(=O)C(C(=O)NCN1CCN(CCO)CC1)=C(O)[C@H]2N(C)C
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via tetracyclines )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing pipacycline (CHEBI:75262) has role antimicrobial agent (CHEBI:33281)
pipacycline (CHEBI:75262) is a N-alkylpiperazine (CHEBI:46845)
pipacycline (CHEBI:75262) is a tertiary α-hydroxy ketone (CHEBI:139592)
pipacycline (CHEBI:75262) is a tetracyclines (CHEBI:26895)
pipacycline (CHEBI:75262) is conjugate base of pipacycline(1+) (CHEBI:75267)
Incoming pipacycline(1+) (CHEBI:75267) is conjugate acid of pipacycline (CHEBI:75262)
INNs Sources
pipaciclina ChemIDplus
pipacycline ChemIDplus
pipacyclinum ChemIDplus
Synonyms Sources
mepicycline ChEBI
N-((4-(2-Hydroxyethyl)-1-piperazinyl)methyl)tetracycline ChemIDplus
N-(4-(beta-Hydroxyethyl)diethylenediamino-1-methyl)tetracycline ChemIDplus
Manual Xref Database
EA012203 Patent
View more database links
Registry Numbers Types Sources
1110-80-1 CAS Registry Number ChemIDplus
1614440 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
13944906 PubMed citation Europe PMC
13949714 PubMed citation Europe PMC
13949715 PubMed citation Europe PMC
4625269 PubMed citation Europe PMC
4958219 PubMed citation Europe PMC
5404598 PubMed citation Europe PMC
5566185 PubMed citation Europe PMC
Last Modified
07 February 2018