Phenothiazine, abbreviated PTZ, is an organic compound that has the formula S(C6H4)2NH and is related to the thiazine-class of heterocyclic compounds. Derivatives of phenothiazine are highly bioactive and have widespread use and rich history.
The derivatives chlorpromazine and promethazine revolutionized the fields of psychiatry and allergy treatment, respectively. An earlier derivative, methylene blue, was one of the first antimalarial drugs, and derivatives of phenothiazine are currently under investigation as possible anti-infective drugs. Phenothiazine is a prototypical pharmaceutical lead structure in medicinal chemistry. |
Read full article at Wikipedia
|
InChI=1S/C14H10O/c15-14-12-7-3-1-5-10(12)9-11-6-2-4-8-13(11)14/h1-8H,9H2 |
RJGDLRCDCYRQOQ-UHFFFAOYSA-N |
|
radical scavenger
A role played by a substance that can react readily with, and thereby eliminate, radicals.
|
|
View more via ChEBI Ontology
9(10H)-anthracenone
|
NIST Chemistry WebBook
|
9,10-dihydro-9-oxoanthracene
|
NIST Chemistry WebBook
|
9-oxoanthracene
|
ChemIDplus
|
anthranone
|
ChemIDplus
|
anthrone
|
NIST Chemistry WebBook
|
Az-O
|
ChEBI
|
carbothrone
|
ChemIDplus
|
1910173
|
Reaxys Registry Number
|
Reaxys
|
875472
|
Gmelin Registry Number
|
Gmelin
|
90-44-8
|
CAS Registry Number
|
NIST Chemistry WebBook
|
90-44-8
|
CAS Registry Number
|
ChemIDplus
|
14500876
|
PubMed citation
|
Europe PMC
|
21452374
|
PubMed citation
|
Europe PMC
|
21462270
|
PubMed citation
|
Europe PMC
|
21659042
|
PubMed citation
|
Europe PMC
|
22494822
|
PubMed citation
|
Europe PMC
|
23212388
|
PubMed citation
|
Europe PMC
|
8234446
|
PubMed citation
|
Europe PMC
|
|