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3-methyl-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one hydrochloride is a chemical compound characterized by its unique triazaspiro ring system and a methyl and phenyl substituent. It is a member of the spiro compounds class, known for its potential therapeutic properties. The hydrochloride salt form enhances its solubility and stability, making it a promising candidate for pharmaceutical applications, particularly in the treatment of neurological disorders and psychiatric conditions.

1023-85-4

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1023-85-4 Usage

Uses

Used in Pharmaceutical Industry:
3-methyl-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one hydrochloride is used as a potential therapeutic agent for the treatment of certain neurological disorders and psychiatric conditions. Its unique chemical structure and improved solubility and stability due to the hydrochloride salt form make it a valuable compound for further research and development in the pharmaceutical field.
Used in Preclinical Research:
3-methyl-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one hydrochloride is utilized in preclinical studies to evaluate its potential efficacy and safety as a treatment for neurological and psychiatric conditions. These studies aim to understand the compound's mechanism of action, pharmacokinetics, and pharmacodynamics, providing valuable insights for its future development as a medication.

Check Digit Verification of cas no

The CAS Registry Mumber 1023-85-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1023-85:
(6*1)+(5*0)+(4*2)+(3*3)+(2*8)+(1*5)=44
44 % 10 = 4
So 1023-85-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H19N3O/c1-16-11-17(12-5-3-2-4-6-12)14(13(16)18)7-9-15-10-8-14/h2-6,15H,7-11H2,1H3

1023-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one,hydrochloride

1.2 Other means of identification

Product number -
Other names 1,3,8-Triazaspiro[4.5]decan-4-one, 3-methyl-1-phenyl-, monohydrochloride

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:1023-85-4 SDS

1023-85-4Downstream Products

1023-85-4Relevant academic research and scientific papers

Novel Autotaxin Inhibitor for the Treatment of Idiopathic Pulmonary Fibrosis: A Clinical Candidate Discovered Using DNA-Encoded Chemistry

Cuozzo, John W.,Clark, Matthew A.,Keefe, Anthony D.,Kohlmann, Anna,Mulvihill, Mark,Ni, Haihong,Renzetti, Louis M.,Resnicow, Daniel I.,Ruebsam, Frank,Sigel, Eric A.,Thomson, Heather A.,Wang, Ce,Xie, Zhifeng,Zhang, Ying

, p. 7840 - 7856 (2020/08/21)

The activity of the secreted phosphodiesterase autotaxin produces the inflammatory signaling molecule LPA and has been associated with a number of human diseases including idiopathic pulmonary fibrosis (IPF). We screened a single DNA-encoded chemical library (DECL) of 225 million compounds and identified a series of potent inhibitors. Optimization of this series led to the discovery of compound 1 (X-165), a highly potent, selective, and bioavailable small molecule. Cocrystallization of compound 1 with human autotaxin demonstrated that it has a novel binding mode occupying both the hydrophobic pocket and a channel near the autotaxin active site. Compound 1 inhibited the production of LPA in human and mouse plasma at nanomolar levels and showed efficacy in a mouse model of human lung fibrosis. After successfully completing IND-enabling studies, compound 1 was approved by the FDA for a Phase I clinical trial. These results demonstrate that DECL hits can be readily optimized into clinical candidates.

SUBSTITUTED SPIROCYDIC INHIBITORS OF AUTOTAXIN

-

, (2015/11/17)

The present invention relates to compounds according to Formula 1 and pharmaceutically acceptable salts, synthesis, intermediates, formulations, and methods of disease treatment therewith, including cancer, lymphocyte homing, chronic inflammation, neuropathic pain, fibrotic diseases, thrombosis, and cholestatic pruritus, mediated at least in part by ATX.

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