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[trans-4-(aminomethyl)cyclohexyl]methanol(SALTDATA: FREE) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17879-23-1

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17879-23-1 Usage

Uses

Used in Organic Synthesis:
[trans-4-(aminomethyl)cyclohexyl]methanol(SALTDATA: FREE) is used as a building block in organic synthesis for the creation of various biologically active molecules. Its unique structure allows for the formation of complex molecules with potential applications in different fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, [trans-4-(aminomethyl)cyclohexyl]methanol(SALTDATA: FREE) is used as a key component in the development of new therapeutic agents. Its potential pharmacological properties make it a valuable compound for the treatment of various medical conditions.
Used in Drug Development:
[trans-4-(aminomethyl)cyclohexyl]methanol(SALTDATA: FREE) is utilized in the development of new drugs, particularly for the treatment of various medical conditions. Its unique chemical structure and potential pharmacological properties contribute to the creation of innovative therapeutic agents with improved efficacy and safety profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 17879-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,7 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17879-23:
(7*1)+(6*7)+(5*8)+(4*7)+(3*9)+(2*2)+(1*3)=151
151 % 10 = 1
So 17879-23-1 is a valid CAS Registry Number.

17879-23-1SDS

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-(Aminomethyl)cyclohexyl]methanol

1.2 Other means of identification

Product number -
Other names AMINOCYCLOHEXANOL(TRANS-4)

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:17879-23-1 SDS

17879-23-1Relevant academic research and scientific papers

Progesterone-adenine hybrids as bivalent inhibitors of P-glycoprotein- mediated multidrug efflux: Design, synthesis, characterization and biological evaluation

Zeinyeh, Wael,Mahiout, Zahia,Radix, Sylvie,Lomberget, Thierry,Dumoulin, Axel,Barret, Roland,Grenot, Catherine,Rocheblave, Luc,Walchshofer, Nadia,Matera, Eva-Laure,Dumontet, Charles

, p. 1177 - 1191,15 (2020/08/20)

Bivalent ligands were designed on the basis of the described close proximity of the ATP-site and the putative steroid-binding site of P-glycoprotein (ABCB1). The syntheses of 19 progesterone-adenine hybrids are described. Their abilities to inhibit P-glycoprotein-mediated daunorubicin efflux in K562/R7 human leukemic cells overexpressing P-glycoprotein were evaluated versus progesterone. The hybrid with a hexamethylene linker chain showed the best inhibitory potency. The efficiency of these progesterone-adenine hybrids depends on two main factors: (i) the nature of the linker and (ii) its attachment point on the steroid skeleton.

Design, synthesis and evaluation of progesterone-adenine hybrids as bivalent inhibitors of P-glycoprotein-mediated multidrug efflux

Zeinyeh, Wa?l,Alameh, Ghina,Radix, Sylvie,Grenot, Catherine,Dumontet, Charles,Walchshofer, Nadia

scheme or table, p. 3165 - 3168 (2010/09/05)

Steroidal bivalent ligands were designed on the basis of the described closer proximity of the ATP-site and the putative steroid-binding site of P-glycoprotein (ABCB1). The syntheses of seven progesterone-adenine hybrids were described. Their abilities to inhibit P-glycoprotein-mediated daunorubicin efflux in K562/R7 human leukemic cells overexpressing P-glycoprotein were evaluated versus progesterone.

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