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ACH 0141625 is a chemical compound that has been studied for its potential as a treatment for inflammatory and autoimmune diseases, as well as cancer. It is a potent and selective inhibitor of Janus kinase 1 (JAK1), which plays a key role in the signaling pathways that regulate immune responses and inflammation. By inhibiting JAK1, ACH 0141625 has the potential to reduce the production of inflammatory cytokines and suppress the overactive immune response seen in many autoimmune diseases. Additionally, ACH 0141625 has shown promise in preclinical studies for its ability to inhibit the growth of cancer cells, making it a potentially important compound for the development of novel therapeutics for a range of diseases.

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  • 1001667-23-7 Structure
  • Basic information

    1. Product Name: ACH 0141625
    2. Synonyms: ACH 0141625;Sovaprevir;Fonadelpar;(2S,4R)-N-[(1R,2S)-1-(cyclopropylsulfonylcarbamoyl)-2-ethenylcyclopropyl]-1-[(2S)-3,3-dimethyl-2-(2-oxo-2-piperidin-1-ylethyl)butanoyl]-4-(7-methoxy-2-phenylquinolin-4-yl)oxypyrrolidine-2-carboxamide
    3. CAS NO:1001667-23-7
    4. Molecular Formula: C43H53N5O8S
    5. Molecular Weight: 799.97462
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1001667-23-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: ACH 0141625(CAS DataBase Reference)
    10. NIST Chemistry Reference: ACH 0141625(1001667-23-7)
    11. EPA Substance Registry System: ACH 0141625(1001667-23-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1001667-23-7(Hazardous Substances Data)

1001667-23-7 Usage

Uses

Used in Pharmaceutical Industry:
ACH 0141625 is used as an anti-inflammatory and immunosuppressive agent for its ability to inhibit the production of inflammatory cytokines and suppress overactive immune responses in autoimmune diseases.
Used in Oncology:
ACH 0141625 is used as an anticancer agent for its potential to inhibit the growth of cancer cells, making it a promising compound for the development of novel therapeutics for various types of cancer.
Used in Drug Development:
ACH 0141625 is used as a lead compound in the development of novel therapeutics for inflammatory and autoimmune diseases, as well as cancer, due to its potent and selective inhibition of Janus kinase 1 (JAK1).

Check Digit Verification of cas no

The CAS Registry Mumber 1001667-23-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,1,6,6 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1001667-23:
(9*1)+(8*0)+(7*0)+(6*1)+(5*6)+(4*6)+(3*7)+(2*2)+(1*3)=97
97 % 10 = 7
So 1001667-23-7 is a valid CAS Registry Number.

1001667-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,4R)-N-[(1R,2S)-1-(cyclopropylsulfonylcarbamoyl)-2-ethenylcyclopropyl]-1-[(2S)-3,3-dimethyl-2-(2-oxo-2-piperidin-1-ylethyl)butanoyl]-4-(7-methoxy-2-phenylquinolin-4-yl)oxypyrrolidine-2-carboxamide

1.2 Other means of identification

Product number -
Other names Sovaprevir (USAN)

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:1001667-23-7 SDS

1001667-23-7Downstream Products

1001667-23-7Relevant articles and documents

4-amino-4-oxobutanoyl peptides as inhibitors of viral replication

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Page/Page column 45; 46; 69; 70, (2015/10/05)

The invention provides 4-amino-4-oxobutanoyl peptides of Formula I and the pharmaceutically salts and hydrates thereof. The variables R, R1, R6-R8, R16, R18, R19, M, n, T, Y, and Z are defined herein. Certain compounds of Formula I are useful as antiviral agents. The 4-amino-4-oxobutanoyl peptides disclosed herein are potent and/or selective inhibitors of viral replication, particularly Hepatitis C virus replication. The invention also provides pharmaceutical compositions containing one or more 4-amino-4-oxobutanoyl peptides and one or more pharmaceutically acceptable carriers. Such pharmaceutical compositions may contain a 4-amino-4-oxobutanoyl peptides as the only active agent or may contain a combination of a 4-amino-4-oxobutanoyl peptides and one or more other pharmaceutically active agents. The invention also provides methods for treating viral infections, including Hepatitis C infections.

NOVEL PROCESSES FOR PRODUCING SOVAPREVIR

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, (2014/10/04)

The disclosure includes novel processes for producing Sovaprevir comprising adding compound E to F-1 to provide Sovaprevir. The disclosure further includes intermediates useful for producing Sovaprevir. The disclosure also includes a novel crystalline form of Sovaprevir, Form F, and a method for preparing spray-dried amorphous Sovaprevir from crystalline Form F.

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