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1-Piperidinesulfonamide, 4-hydroxy-(7CI,8CI) is a chemical compound with the molecular formula C5H11NO3S. It is a derivative of piperidine, a cyclic amine, and sulfonamide, a class of compounds with antibacterial properties. This specific compound features a hydroxyl group at the 4-position and a sulfonamide group at the 1-position of the piperidine ring. It is primarily used in the pharmaceutical industry as an intermediate in the synthesis of various drugs, particularly those with potential applications in the treatment of bacterial infections. The compound's unique structure allows it to interact with bacterial enzymes, inhibiting their function and ultimately leading to the death of the bacteria. Due to its potential applications in medicine, research on 1-piperidinesulfonamide, 4-hydroxy-(7CI,8CI) and its derivatives is ongoing to explore their therapeutic potential and optimize their properties for various medical uses.

4108-97-8

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4108-97-8 Usage

Chemical structure

Contains a piperidine ring and a sulfonamide group

Pharmaceutical applications

Has potential as a carbonic anhydrase inhibitor

Therapeutic uses

Can be used as diuretics, in the treatment of glaucoma, and in the management of certain types of epilepsy

Biological activity

The hydroxy group can influence solubility and binding interactions

Further research

Needed to fully understand its pharmacological properties and potential applications

Check Digit Verification of cas no

The CAS Registry Mumber 4108-97-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,0 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4108-97:
(6*4)+(5*1)+(4*0)+(3*8)+(2*9)+(1*7)=78
78 % 10 = 8
So 4108-97-8 is a valid CAS Registry Number.

4108-97-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-piperidine-1-sulfonic acid amide

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-piperidine-1-sulfonic acid amide

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:4108-97-8 SDS

4108-97-8Upstream product

4108-97-8Downstream Products

4108-97-8Relevant academic research and scientific papers

Diversely substituted sulfamides for fragment-based drug discovery of carbonic anhydrase inhibitors: synthesis and inhibitory profile

Angeli, Andrea,Ferraroni, Marta,Kalinin, Stanislav,Korsakov, Mikhail,Krasavin, Mikhail,Nocentini, Alessio,Sharonova, Tatiana,Supuran, Claudiu T.,Zhmurov, Petr

, p. 857 - 865 (2022/03/27)

A series of sulfamide fragments has been synthesised and investigated for human carbonic anhydrase inhibition. One of the fragments showing greater selectivity for cancer-related isoforms hCA IX and XII was co-crystalized with hCA II showing significant potential for fragment periphery evolution via fragment growth and linking. These opportunities will be identified in the future via the screening of this fragment structure for co-operative carbonic anhydrase binding with other structurally diverse fragments.

COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH APJ RECEPTOR ACTIVITY

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Page/Page column 189, (2020/05/15)

This disclosure features chemical entities (e.g., a compound or a pharmaceutically acceptable salt and/or hydrate and/or prodrug of the compound) that modulate (e.g., agonize) the apelin receptor (also referred to herein as the APJ receptor; gene symbol APLNR). This disclosure also features compositions containing the same as well as other methods of using and making the same. The chemical entities are useful, e.g., for treating a subject (e.g., a human) having a disease, disorder, or condition in which a decrease in APJ receptor activity (e.g., repressed or impaired APJ receptor signaling; e.g., repressed or impaired apelin-APJ receptor signaling) or downregulation of endogenous apelin contributes to the pathology and/or symptoms and/or progression of the disease, disorder, or condition. Non-limiting examples of such diseases, disorders, or conditions include: (i) cardiovascular disease; (ii) metabolic disorders; (iii) diseases, disorders, and conditions associated with vascular pathology; and (iv) organ failure; (v) diseases, disorders, and conditions associated with infections (e.g., microbial infections); and (vi) diseases, disorders, or conditions that are sequela or comorbid with any of the foregoing or any disclosed herein. More particular non-limiting examples of such diseases, disorders, or conditions include pulmonary hypertension (e.g., PAH); heart failure; type II diabetes; renal failure; sepsis; and systemic hypertension.

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