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8-Hydroxyloxapine, also known as 8-OH loxapine, is a metabolite derived from loxapine, an atypical antipsychotic medication. It is formed through the metabolism of loxapine by the cytochrome P450 isoform CYP1A2. 8-Hydroxyloxapine exhibits a pale yellow solid appearance and has relatively low affinity for dopamine and 5-HT receptors compared to the parent compound. However, it does inhibit [14C]5-HT uptake in vitro, with an IC50 of 2 μM in human platelets.

61443-77-4

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61443-77-4 Usage

Uses

Used in Pharmaceutical Industry:
8-Hydroxyloxapine is used as a metabolite in the development and understanding of atypical antipsychotic medications. Its role in the metabolism of loxapine provides insights into the drug's efficacy and potential side effects, contributing to the optimization of antipsychotic treatments.
Used in Research and Development:
8-Hydroxyloxapine serves as a valuable compound for researchers studying the mechanisms of action and receptor interactions of atypical antipsychotic drugs. Its relatively low affinity for dopamine and 5-HT receptors makes it a useful tool for investigating the contributions of these receptors to the therapeutic effects and side effects of loxapine.
Used in Drug Metabolism Studies:
8-Hydroxyloxapine is used as a subject in drug metabolism studies to understand the role of cytochrome P450 isoform CYP1A2 in the metabolism of atypical antipsychotic medications. This knowledge can help in the development of personalized medicine approaches, tailoring drug treatments to individual patients based on their unique metabolic profiles.
Used in Drug Interaction Studies:
8-Hydroxyloxapine can be employed in studies investigating potential drug interactions involving loxapine and other medications that are metabolized by the same cytochrome P450 isoform, CYP1A2. Understanding these interactions can help healthcare providers make informed decisions about drug combinations and dosing regimens to maximize therapeutic benefits and minimize adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 61443-77-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,4 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61443-77:
(7*6)+(6*1)+(5*4)+(4*4)+(3*3)+(2*7)+(1*7)=114
114 % 10 = 4
So 61443-77-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H18ClN3O2/c1-21-6-8-22(9-7-21)18-14-10-12(19)2-4-16(14)24-17-5-3-13(23)11-15(17)20-18/h2-5,10-11,23H,6-9H2,1H3

61443-77-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-chloro-6-(4-methylpiperazin-1-yl)benzo[b][1,4]benzoxazepin-3-ol

1.2 Other means of identification

Product number -
Other names Dibenz(b,f)(1,4)oxazepin-8-ol,2-chloro-11-(4-methyl-1-piperazinyl)

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:61443-77-4 SDS

61443-77-4Upstream product

61443-77-4Downstream Products

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