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Decarboxylated AdoMet

Decarboxylated AdoMet structure

Decarboxylated AdoMet 

structure
  • CAS No:

    22365-13-5

  • Formula:

    C14H23N6O3S

  • Chemical Name:

    Decarboxylated AdoMet

  • Synonyms:

    Adenosine,5′-[(3-aminopropyl)methylsulfonio]-5′-deoxy-;5′-[(3-Aminopropyl)methylsulfonio]-5′-deoxyadenosine;(-)-S-Adenosyl-(5′)-3-methylthiopropylamine;S-Methyladenosylhomocysteamine;S-Adenosyl-3-methylthiopropylamine;S-Adenosylmethionamine;Decarboxylated AdoMet;S-Methyl-S-adenosylhomocysteamine;S-Adenosyl-L-methionamine;dAdoMet;15519-62-7;361436-42-2;1363853-42-2

  • Categories:

    Biochemical Engineering  >  Saccharides

Description

ChEBI: The S-adenosyl derivative of methioninamine.


Solid


S-adenosylmethioninamine is the S-adenosyl derivative of methioninamine. It has a role as an Escherichia coli metabolite and a mouse metabolite. It is a sulfonium compound and a member of adenosines. It derives from a 3-methylthiopropylamine. It is a conjugate base of a S-adenosylmethioninaminium.

Decarboxylated AdoMet Basic Attributes

355.437

355.155

Characteristics

146

-0.8

Solid

Drug Information

decarboxylated S-adenosylmethionine

Computed Properties

Molecular Weight:355.44
XLogP3:-0.8
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:6
Exact Mass:355.15523479
Monoisotopic Mass:355.15523479
Topological Polar Surface Area:146
Heavy Atom Count:24
Formal Charge:1
Complexity:422
Defined Atom Stereocenter Count:4
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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