What is the S-ADENOSYL-L-METHIONINE?

S-ADENOSYL-L-METHIONINE is , while it's Molecular Formula is C 15 H 22 N 6 O 5 S. Used in Pharmaceutical Industry: S-ADENOSYL-L-METHIONINE is used as a therapeutic agent for the treatment of depression and arthritis. Its application is based on its ability to participate in essential cellular reactions, which contribute to its therapeutic effects on these conditions. Used in Metabolic Research: S-ADENOSYL-L-METHIONINE is used as a key compound in metabolic research for understanding the roles of methylation, sulfur group storage, and transfer in cellular processes. Its involvement in various cellular reactions makes it an important molecule for studying metabolic pathways and their regulation. Used in Drug Development: S-ADENOSYL-L-METHIONINE is used as a starting material or intermediate in the synthesis of various drugs and pharmaceutical compounds. Its unique chemical properties and involvement in essential cellular reactions make it a valuable component in the development of new therapeutic agents. Used in Nutritional Supplements: S-ADENOSYL-L-METHIONINE is used as an ingredient in nutritional supplements, particularly those aimed at supporting mood, joint health, and overall cellular function. Its role in cellular reactions and its therapeutic effects on depression and arthritis contribute to its use in these products.

What is the CAS number for S-ADENOSYL-L-METHIONINE?

The CAS number of S-ADENOSYL-L-METHIONINE is 17176-17-9.

What is S-ADENOSYL-L-METHIONINE (17176-17-9) used for?

S-ADENOSYL-L-METHIONINE, also known as SAM, is an essential metabolite that is found in all biological cells. It plays a crucial role in various cellular reactions, including transmethylation, transsulfurization, and transaminopropyl reactions. SAM is indispensable for the methylation modification, sulfur group storage, and transfer of important intracellular molecules.InChI:InChI=1/C15H22N6O5S.C7H8O3S/c1-27(3-2-7(16)15(24)25)4-8-10(22)11(23)14(26-8)21-6-20-9-12(17)18-5-19-13(9)21;1-6-2-4-7(5-3-6)11(8,9)10/h5-8,10-11,14,22-23H,2-4,16H2,1H3,(H2-,17,18,19,24,25);2-5H,1H3,(H,8,9,10)/t7-,8+,10+,11+,14+,27?;/m0./s1

What is the S-ADENOSYL-L-METHIONINE?

S-ADENOSYL-L-METHIONINE is , while it's Molecular Formula is C 15 H 22 N 6 O 5 S. Used in Pharmaceutical Industry: S-ADENOSYL-L-METHIONINE is used as a therapeutic agent for the treatment of depression and arthritis. Its application is based on its ability to participate in essential cellular reactions, which contribute to its therapeutic effects on these conditions. Used in Metabolic Research: S-ADENOSYL-L-METHIONINE is used as a key compound in metabolic research for understanding the roles of methylation, sulfur group storage, and transfer in cellular processes. Its involvement in various cellular reactions makes it an important molecule for studying metabolic pathways and their regulation. Used in Drug Development: S-ADENOSYL-L-METHIONINE is used as a starting material or intermediate in the synthesis of various drugs and pharmaceutical compounds. Its unique chemical properties and involvement in essential cellular reactions make it a valuable component in the development of new therapeutic agents. Used in Nutritional Supplements: S-ADENOSYL-L-METHIONINE is used as an ingredient in nutritional supplements, particularly those aimed at supporting mood, joint health, and overall cellular function. Its role in cellular reactions and its therapeutic effects on depression and arthritis contribute to its use in these products.

What is the CAS number for S-ADENOSYL-L-METHIONINE?

The CAS number of S-ADENOSYL-L-METHIONINE is 17176-17-9.

What is S-ADENOSYL-L-METHIONINE (17176-17-9) used for?

S-ADENOSYL-L-METHIONINE, also known as SAM, is an essential metabolite that is found in all biological cells. It plays a crucial role in various cellular reactions, including transmethylation, transsulfurization, and transaminopropyl reactions. SAM is indispensable for the methylation modification, sulfur group storage, and transfer of important intracellular molecules.InChI:InChI=1/C15H22N6O5S.C7H8O3S/c1-27(3-2-7(16)15(24)25)4-8-10(22)11(23)14(26-8)21-6-20-9-12(17)18-5-19-13(9)21;1-6-2-4-7(5-3-6)11(8,9)10/h5-8,10-11,14,22-23H,2-4,16H2,1H3,(H2-,17,18,19,24,25);2-5H,1H3,(H,8,9,10)/t7-,8+,10+,11+,14+,27?;/m0./s1

Manufacturer supply S-Adenosylmethionine 17176-17-9 with sufficient stock and high standard

 

Home
About us
Markets

Pharmaceuticals

Nutraceuticals

Cosmetics
Sustainability
Blog

Company News

Professional articles
Application & Solutions

Capsules

Tablets

Gummies

Softgels

Premix

Syrup

Lotions

Cream

Masks
Careers
Contact Us

PRODUCT

Current location：Home > Markets > Nutraceuticals

S-Adenosylmethionine

CasNo.:17176-17-9
Purity:
Content:
MF:C₁₅H₂₂N₆O₅S
Packing:
MW:398.443
Apply:

Inquiry

Manufacturer supply S-Adenosylmethionine 17176-17-9 with sufficient stock and high standard

Molecular Formula:C₁₅H₂₂N₆O₅S
Molecular Weight:398.443
Melting Point:78℃
PSA：273.51000
LogP:1.33920

S-ADENOSYL-L-METHIONINE(Cas 17176-17-9) Usage

Biological Activity

S-Adenosyl-DL-methionine is a derivative of Ademetionine (HY-B0617). Ademetionine is an intermediate metabolite of methionine.

InChI:InChI=1/C15H22N6O5S.C7H8O3S/c1-27(3-2-7(16)15(24)25)4-8-10(22)11(23)14(26-8)21-6-20-9-12(17)18-5-19-13(9)21;1-6-2-4-7(5-3-6)11(8,9)10/h5-8,10-11,14,22-23H,2-4,16H2,1H3,(H2-,17,18,19,24,25);2-5H,1H3,(H,8,9,10)/t7-,8+,10+,11+,14+,27?;/m0./s1

17176-17-9 Relevant articles

Thermostable enzyme-immobilized magnetic responsive Ni-based metal-organic framework nanorods as recyclable biocatalysts for efficient biosynthesis of: S -adenosylmethionine

He, Jie,Sun, Shanshan,Zhou, Zhao,Yuan, Qipeng,Liu, Yanhui,Liang, Hao

supporting information, p. 2077 - 2085 (2019/02/12)

A novel magnetic responsive Ni-based met...

Mechanism of a Class C Radical S-Adenosyl- l -methionine Thiazole Methyl Transferase

Zhang, Zhengan,Mahanta, Nilkamal,Hudson, Graham A.,Mitchell, Douglas A.,Van Der Donk, Wilfred A.

, p. 18623 - 18631 (2017/12/26)

The past decade has seen the discovery o...

Facile chemoenzymatic strategies for the synthesis and utilization of S-adenosyl-L-methionine analogues

Singh, Shanteri,Zhang, Jianjun,Huber, Tyler D.,Sunkara, Manjula,Hurley, Katherine,Goff, Randal D.,Wang, Guojun,Zhang, Wen,Liu, Chunming,Rohr, Juergen,Van Lanen, Steven G.,Morris, Andrew J.,Thorson, Jon S.

supporting information, p. 3965 - 3969 (2014/05/06)

A chemoenzymatic platform for the synthe...

Chemical Synthesis Of S-Adenosyl-L-Methionine With Enrichment Of (S,S)-Isomer

-

Page/Page column 4; 5, (2008/06/13)

This invention relates to an improved pr...

17176-17-9 Process route

: 63-68-3,26062-47-5,58576-49-1
L-methionine

: 56-65-5,896506-78-8
ATP

: 14031-35-7,17176-17-9,29908-03-0,75044-81-4,78548-84-2,79647-17-9,91279-78-6
S-Adenosyl-L-methionine

: 2457-80-9
5'-Deoxy-5'-methylthioadenosine

Conditions

Conditions	Yield
With recombinant Methanocaldococcus jannaschii methionine adenosyltransferase; potassium chloride; magnesium chloride; In aq. buffer; at 65 ℃; for 4h; pH=8; Temperature; Reagent/catalyst; Enzymatic reaction;

: 6914-65-4
1-methylhexahydropyrylium tetrafluoroborate

: 979-92-0
S-(5'-adenosyl)-L-homocysteine

: 14031-35-7,17176-17-9,29908-03-0,75044-81-4,78548-84-2,79647-17-9,91279-78-6
S-Adenosyl-L-methionine

Conditions

Conditions	Yield
1-methylhexahydropyrylium tetrafluoroborate; S-(5'-adenosyl)-L-homocysteine; With sulfuric acid; trifluoroacetic acid; at 0 ℃; In dichloromethane; water; Product distribution / selectivity;