Descriptor English: | 3,4-Methylenedioxyamphetamine | ||||||
Descriptor Spanish: |
3,4-Metilenodioxianfetamina
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Descriptor Portuguese: | 3,4-Metilenodioxianfetamina | ||||||
Descriptor French: | 3,4-Méthylènedioxy-amphétamine | ||||||
Entry term(s): |
3,4 Methylenedioxyamphetamine |
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Tree number(s): |
D02.092.471.683.152.660 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D015104 | ||||||
Scope note: | An amphetamine derivative that inhibits uptake of catecholamine neurotransmitters. It is a hallucinogen. It is less toxic than its methylated derivative but in sufficient doses may still destroy serotonergic neurons and has been used for that purpose experimentally. |
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Allowable Qualifiers: |
AA analogs & derivatives AD administration & dosage AE adverse effects AG agonists AI antagonists & inhibitors AN analysis BL blood CF cerebrospinal fluid CH chemistry CL classification CS chemical synthesis EC economics HI history IM immunology IP isolation & purification ME metabolism PD pharmacology PK pharmacokinetics PO poisoning RE radiation effects SD supply & distribution ST standards TO toxicity TU therapeutic use UR urine |
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Pharm Action: |
Hallucinogens Serotonin Agents Adrenergic Uptake Inhibitors |
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Registry Number: | 4764-17-4 | ||||||
CAS Type 1 Name: | 1,3-Benzodioxole-5-ethanamine, alpha-methyl- | ||||||
Previous Indexing: |
Amphetamine (1973-1976) Dioxoles (1974-1975) Methyl Ethers (1973) |
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Public MeSH Note: | 91; was see under AMPHETAMINES 1977-90 |
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History Note: | 91(77); was see under AMPHETAMINES 1977-90 |
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DeCS ID: | 8939 | ||||||
Unique ID: | D015104 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 1991/01/01 | ||||||
Date of Entry: | 1976/04/13 | ||||||
Revision Date: | 2000/06/22 |
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CHEMICALS AND DRUGS
Organic Chemicals [D02]Organic Chemicals
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3,4-Methylenedioxyamphetamine
- Preferred
Concept UI |
M0023232 |
Scope note | An amphetamine derivative that inhibits uptake of catecholamine neurotransmitters. It is a hallucinogen. It is less toxic than its methylated derivative but in sufficient doses may still destroy serotonergic neurons and has been used for that purpose experimentally. |
Preferred term | 3,4-Methylenedioxyamphetamine |
Entry term(s) |
3,4 Methylenedioxyamphetamine |
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