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S-Adenosylhomocysteine
MeSH Descriptor Data 2024
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
S-Adenosylhomocysteine
Tree Number(s)
D02.886.030.498.050
D03.633.100.759.590.138.240
D12.125.166.498.050
D13.570.583.138.240
D13.570.800.096.262
Unique ID
D012435
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D012435
Scope Note
5'-S-(3-Amino-3-carboxypropyl)-5'-thioadenosine. Formed from S-adenosylmethionine after transmethylation reactions.
Entry Term(s)
S Adenosylhomocysteine
CAS Type 1 Name
L-Homocysteine, S-(5'-deoxyadenosin-5'-yl)-
Previous Indexing
Adenosine (1972-1974)
Homocysteine (1972-1974)
Public MeSH Note
91; was see under HOMOCYSTEINE 1975-90
History Note
91(75); was see under HOMOCYSTEINE 1975-90
Date Established
1991/01/01
Date of Entry
1974/11/19
Revision Date
2016/05/31
Allowable Qualifiers
administration & dosage (AD)
adverse effects (AE)
agonists (AG)
analogs & derivatives (AA)
analysis (AN)
antagonists & inhibitors (AI)
blood (BL)
cerebrospinal fluid (CF)
chemical synthesis (CS)
chemistry (CH)
classification (CL)
economics (EC)
history (HI)
immunology (IM)
isolation & purification (IP)
metabolism (ME)
pharmacokinetics (PK)
pharmacology (PD)
poisoning (PO)
radiation effects (RE)
standards (ST)
supply & distribution (SD)
therapeutic use (TU)
toxicity (TO)
urine (UR)
Organic Chemicals [D02]
Sulfur Compounds [D02.886]
Amino Acids, Sulfur [D02.886.030]
Homocysteine [D02.886.030.498]
S-Adenosylhomocysteine [D02.886.030.498.050]
Heterocyclic Compounds [D03]
Heterocyclic Compounds, Fused-Ring [D03.633]
Heterocyclic Compounds, 2-Ring [D03.633.100]
Purines [D03.633.100.759]
Purine Nucleosides [D03.633.100.759.590]
Adenosine [D03.633.100.759.590.138]
Adenosine-5'-(N-ethylcarboxamide) [D03.633.100.759.590.138.025]
S-Adenosylhomocysteine [D03.633.100.759.590.138.240]
S-Adenosylmethionine [D03.633.100.759.590.138.264]
2-Chloroadenosine [D03.633.100.759.590.138.300]
Deoxyadenosines [D03.633.100.759.590.138.325]
Isopentenyladenosine [D03.633.100.759.590.138.500]
Phenylisopropyladenosine [D03.633.100.759.590.138.630]
Puromycin [D03.633.100.759.590.138.711]
Ticagrelor [D03.633.100.759.590.138.806]
Vidarabine [D03.633.100.759.590.138.900]
Amino Acids, Peptides, and Proteins [D12]
Amino Acids [D12.125]
Amino Acids, Sulfur [D12.125.166]
Homocysteine [D12.125.166.498]
S-Adenosylhomocysteine [D12.125.166.498.050]
Nucleic Acids, Nucleotides, and Nucleosides [D13]
Nucleosides [D13.570]
Purine Nucleosides [D13.570.583]
Adenosine [D13.570.583.138]
Adenosine-5'-(N-ethylcarboxamide) [D13.570.583.138.025]
S-Adenosylhomocysteine [D13.570.583.138.240]
S-Adenosylmethionine [D13.570.583.138.264]
2-Chloroadenosine [D13.570.583.138.300]
Deoxyadenosines [D13.570.583.138.325]
Isopentenyladenosine [D13.570.583.138.500]
Phenylisopropyladenosine [D13.570.583.138.630]
Puromycin [D13.570.583.138.711]
Ticagrelor [D13.570.583.138.806]
Vidarabine [D13.570.583.138.900]
Nucleic Acids, Nucleotides, and Nucleosides [D13]
Nucleosides [D13.570]
Ribonucleosides [D13.570.800]
Adenosine [D13.570.800.096]
Adenosine-5'-(N-ethylcarboxamide) [D13.570.800.096.250]
S-Adenosylhomocysteine [D13.570.800.096.262]
S-Adenosylmethionine [D13.570.800.096.264]
2-Chloroadenosine [D13.570.800.096.300]
Isopentenyladenosine [D13.570.800.096.500]
Phenylisopropyladenosine [D13.570.800.096.630]
Ticagrelor [D13.570.800.096.815]
Expand All
Collapse All
S-Adenosylhomocysteine
Preferred
Concept UI
M0019321
Scope Note
5'-S-(3-Amino-3-carboxypropyl)-5'-thioadenosine. Formed from S-adenosylmethionine after transmethylation reactions.
Terms
S-Adenosylhomocysteine
Preferred Term
Term UI
T036951
Date
01/01/1999
LexicalTag
NON
ThesaurusID
NLM (1975)
S Adenosylhomocysteine
Term UI
T036950
Date
01/26/1978
LexicalTag
NON
ThesaurusID
UNK (19XX)
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