ChemAbout
© 2026 ChemAbout
Insights|Privacy Policy|Terms of Service|[email protected]
Home/Compounds/Research Reagent/5'-Deoxy-5'-methylthioadenosine-d3
C11H15N5O3S
300.35 g/mol
Research Reagent

5'-Deoxy-5'-methylthioadenosine-d3

CAS2699607-01-5
Category
Research Reagent
Compound Class
Heterocycle
Primary Use
Research Compound

5'-Deoxy-5'-methylthioadenosine-d3 is an isotope-labeled research reagent, specifically the trideuteromethyl analog of 5'-deoxy-5'-methylthioadenosine. It is used primarily in analytical and metabolic studies where the deuterium label allows for tracking and quantification.

isotope-labeled internal standard for mass spectrometrytracer in biochemical and metabolic research

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

Sourcing or supplying this compound?

List your inventory or post a purchase request

CAS 2699607-01-5

List This Product
Sign in to publish supply information
Request This Product
Submit a request without registering

Related Compounds

StrongSame Parent

5'-Deoxy-5'-methylthioadenosine-d3

CAS174838-38-1

research compound

ApplicationSame Use

Iodo(113C)methane

CAS4227-95-6

research compound

ApplicationSame Use

Sodium nitrite-15N

CAS68378-96-1

research compound

ApplicationSame Use

L-(β,β-²H₂)Tyrosine

CAS72963-27-0

research compound

ReferenceSame Category

Methyl 3,5-dinitrobenzoate

CAS2702-58-1

research compound

ReferenceSame Category

(S)-1-(3-(Difluoromethyl)-2-fluorophenyl)ethan-1-amine hydrochloride

CAS2703745-91-7

research compound

ReferenceSame Category

N-Nitroso Naphazoline

CAS2703749-87-3

research compound

ReferenceSame Category

4-(1-Amino-2,2,2-trifluoroethyl)phenol hydrochloride

CAS2703756-58-3

research compound

Identifiers
IUPAC Name

(2R,3R,4S,5S)-2-(6-aminopurin-9-yl)-5-(trideuteriomethylsulfanylmethyl)oxolane-3,4-diol

InChIKey

WUUGFSXJNOTRMR-YZLHILBGSA-N

SMILES

[2H]C([2H])([2H])SC[C@@H]1[C@H]([C@H]([C@@H](O1)N2C=NC3=C(N=CN=C32)N)O)O

Synonyms (3)

—