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389890-42-0

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389890-42-0 Usage

General Description

(TRANS)-3-aminocyclobutanol is a chemical compound that belongs to the class of aminocyclobutanol derivatives, which are characterized by a four-membered cyclobutane ring with an amino group attached. (TRANS)-3-AMINOCYCLOBUTANOL can exist in different stereoisomeric forms, with the "trans" configuration referring to the relative positioning of the amino group and the hydroxyl group. (TRANS)-3-aminocyclobutanol has potential applications in organic synthesis, particularly in the development of new pharmaceuticals and biologically active compounds. Its unique structure and properties make it an interesting target for research and drug discovery efforts. Additionally, its small and rigid cyclobutane ring may confer specific biological activities, making it a valuable scaffold for the design of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 389890-42-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,9,8,9 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 389890-42:
(8*3)+(7*8)+(6*9)+(5*8)+(4*9)+(3*0)+(2*4)+(1*2)=220
220 % 10 = 0
So 389890-42-0 is a valid CAS Registry Number.

389890-42-0Relevant articles and documents

Novel CDK inhibitory compounds, preparation method thereof, pharmaceutical composition for use in preventing or treating CDK relating diseases containing the same as an active ingredient

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, (2018/10/24)

The present invention relates to a novel CDK inhibitory compound, a method for manufacturing the same, and a pharmaceutical composition for preventing or treating a CDK-related disease containing the compound as an active ingredient. The novel CDK inhibit

INHIBITORS OF THE TEC KINASE ENZYME FAMILY

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Page/Page column 56, (2016/12/22)

The present invention relates to a novel family of kinases inhibitors. Compounds of this class have been found to have inhibitory activity against members of the TEC kinase family, particularly BTK. The present invention is directed to a compound of Formula I or pharmaceutically acceptable salt, solvate, solvate of salt, stereoisomer, tautomer, isotope, prodrug, complex or biologically active metabolite thereof, for use in therapy.

COMPOUNDS, COMPOSITIONS AND METHODS FOR INCREASING CFTR ACTIVITY

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, (2016/11/07)

The present disclosure features compounds such as those having the Formulae (Ila), (lIb), (lIc), (Ild), (IlIa), and (Illb), which can increase cystic fibrosis transmembrane conductance regulator (CFTR) activity as measured in human bronchial epithelial (hBE) cells. The present disclosure also features methods of treating a condition associated with decreased CFTR activity or a condition associated with a dysfunction of proteostasis comprising administering to a subject an effective amount of a disclosed compound, such as a compound of Formula (Ila), (lIb), (lIc), (lId), (IlIa), or (Illb).

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