Tranylcypromine

HCID 5530

Basic information

CAS
155-09-9
Standard SMILES
NC1CC1c1ccccc1
InChIKey
AELCINSCMGFISI-UHFFFAOYSA-N
Molecular formula
C9H11N
Average molar mass
133.19 g/mol
Monoisotopic mass
133.08914935

Overview

2-phenylcyclopropan-1-amine is a member of the class of cyclopropanes carrying amino and phenyl substituents at positions 1 and 2 respectively. It is a member of benzenes, a primary amine and a member of cyclopropanes.

Names & identifiers

Preferred name
Tranylcypromine
IUPAC
2-phenylcyclopropan-1-amine
English name
2-Phenylcyclopropane-1-amine
Molecular formula
C9H11N
Molecular weight
133.19

Names & synonyms

tranylcyprominedl-TranylcypromineTransamineRacemic TranylcypromineJatrosomParniteneSKF 385TranilciprominaTranylcyprominumNSC80664NSC-80664Cyclopropanamine, 2-phenyl-, trans-(+-)-
Show more names
2-Phenylcyclopropan-1-amine2-PhenylcyclopropylamineCyclopropanamine, 2-phenyl-2-Phenylcyclopropane-1-amine1-Amino-2-phenylcyclopropane
Cyclopropylamine, 2-phenyl-, trans-(+-)-DTXSID2023694Tranylcypromintrans 2 PhenylcyclopropylamineRefChem:561463-12-00-02797 (Beilstein Handbook Reference)CHEBI:9652N06AF04

Database identifiers

CAS
155-09-9、54-97-7
PubChem CID
5530
DTXSID
DTXSID30859306
ChEMBL
CHEMBL313833、CHEMBL3989843
ChEBI
CHEBI:131512
EC Number
205-841-9、822-855-6
Nikkaji
J1I

Properties

Computed structural properties

XLogP
1.5
Topological polar surface area
26 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
1
Rotatable bonds
1
Heavy atoms
10

Experimental & physicochemical properties

DrugsPharmaceuticals
LogP · 2 items

log Kow= 1.58 @ 25 °C

1.49

Color/FormLiquid
Solubility · 3 items

Sol in water /Sulfate/

Very slightly sol in alcohol, ether /Sulfate/

Practically insol in chloroform /Sulfate/

Human DrugsBreast Feeding; Lactation; Antidepressive Agents; Monoamine Oxidase Inhibitors
Boiling Point79-80 °C @ 1.5-1.6 mm Hg

Physicochemical properties

Boiling point
218.3 · 218.3±29.0 °C(Predicted)
Density
1.065 · 1.065±0.06 g/cm3(Predicted)
storage temp.
2 · 2-8°C(protect from light)
pka
8.24 · 8.24±0.10(Predicted)
Appearance
White to off-white Solid
Symbol(GHS)
7 · GHS07

Safety & regulation

GHS classification

GHS Classification · 4 items

Warning

H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]

P264, P264+P265, P270, P280, P301+P317, P302+P352, P305+P351+P338, P321, P330, P332+P317, P337+P317, P362+P364, and P501 (click each P-code to see the statement)

The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Hazard information

Regulatory InformationTranylcypromine: Does not have an individual approval but may be used under an appropriate group standard
Other Safety InformationIMAP assessments - Cyclopropanamine, 2-phenyl-, trans-(.+-.)-: Human health tier I assessment
FDA Requirements · 1 item

Manufacturers, packers, and distributors of drug and drug products for human use are responsible for complying with the labeling, certification, and usage requirements as prescribed by the Federal Food, Drug, and Cosmetic Act, as amended (secs 201-902, 52 Stat. 1040 et seq., as amended; 21 U.S.C. 321-392).

Hazard Classes and CategoriesAcute Tox. 4 (100%)

Safety & protection

Disposal Methods · 1 item

SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

Toxicology

Treatment · 1 item

Treatment should normally consist of general supportive measures, close observation of vital signs and steps to counteract specific symptoms as they occur, since MAO inhibition may persist. External cooling is recommended if hyperpyrexia occurs. Barbiturates have been reported to help relieve myoclonic reactions, but frequency of administration should be controlled carefully because Tranylcypromine may prolong barbiturate activity. When hypotension requires treatment, the standard measures for managing circulatory shock should be initiated. If pressor agents are used, the rate of infusion should be regulated by careful observation of the patient because an exaggerated pressor response sometimes occurs in the presence of MAO inhibition. (L1712)

Interactions · 5 items

HEXOBARBITAL SLEEPING TIME IS PROLONGED BY PARNATE, INDICATING ITS ABILITY TO POTENTIATE OTHER DRUGS PRESUMABLY BY INTERFERING WITH THEIR DETOXIFICATION. /PARNATE/

MAO INHIBITORS ALSO ENHANCE EFFECTS OF EXOGENOUSLY ADMIN AMINES, SUCH AS 5-HT & NOREPINEPHRINE, AS WELL AS PRECURSORS, SUCH AS 3,4-HYDROXYPHENYLALANINE (DOPA) & 5-HYDROXYTRYPTOPHAN. /MAO INHIBITORS/

Meperidine should never be used for ... headaches /with the hypertensive episode/, and blood pressure should be evaluated immediately when a patient taking an MAO inhibitor reports a severe throbbing headache or a feeling of pressure in the head. /MAO INHIBITORS/

MAO INHIBITORS ... INTERFERE WITH DETOXICATION MECHANISMS FOR CERTAIN OTHER DRUGS. THEY PROLONG & INTENSIFY EFFECTS OF CENTRAL DEPRESSANT AGENTS, SUCH AS GENERAL ANESTHETICS, SEDATIVES, ANTIHISTAMINES, ALCOHOL, & POTENT ANALGESICS; OF ANTICHOLINERGIC AGENTS, PARTICULARLY THOSE USED IN THE TREATMENT OF PARKINSONISM; & OF ANTIDEPRESSANT AGENTS, ESP IMIPRAMINE & AMITRIPTYLINE. /MAO INHIBITORS/

For more Interactions (Complete) data for TRANYLCYPROMINE (37 total), please visit the HSDB record page.

Health Effects · 1 item

Rare cases have been reported of hypertensive crisis, serotonin syndrome, myoclonus, hyperpyrexia, psychosis, and delirium, some of which progressed to coma. Additionally, in sensitive individuals or at extreme dosages, hypotension may lead to shock. [Wikipedia]

Hepatotoxicity · 1 item

Tranylcypromine, like most monoamine oxidase inhibitors, can cause transient serum aminotransferase elevations in a proportion of patients. These elevations are usually mild, asymptomatic and self-limited and do not require dose modification. Tranylcypromine has also been associated with rare cases of acute, clinically apparent liver injury. The few cases described have resembled those caused by other MAO inhibitors. The time to clinical onset is typically 1 to 4 months and the usual pattern of serum enzyme elevations is hepatocellular (Case 1), although cholestatic injury has also been described. Immunoallergic features (rash, fever, eosinophilia) are uncommon as is autoantibody formation.

Adverse Effects · 1 item

Common adverse effects of tranylcypromine include dry mouth, headaches, diarrhea, urinary hesitancy, insomnia, agitation, anxiety, nausea, and sexual dysfunction. Postural hypotension, sometimes leading to syncope, is another common adverse effect that warrants special attention for older patients on this medication. This adverse effect is dose-related and may require splitting the dose into 3 to 4 doses daily. More serious side effects include hepatotoxicity, seizures, and induction of mania. Additionally, in the United States, there is a black-box warning stating that this medication may lead to the activation of suicidal ideation and behavior in children, adolescents, and young adults aged 18 to 24 with major depressive disorder and other psychiatric disorders.

Exposure Routes · 1 item

Interindividual variability in absorption. May be biphasic in some individuals. Peak plasma concentrations occur in one hour following oral administration with a secondary peak occurring within 2-3 hours. Biphasic absorption may represent different rates of absorption of the stereoisomers of the drug, though additional studies are required to confirm this.

Regulatory information

FDA Requirements · 1 item

Manufacturers, packers, and distributors of drug and drug products for human use are responsible for complying with the labeling, certification, and usage requirements as prescribed by the Federal Food, Drug, and Cosmetic Act, as amended (secs 201-902, 52 Stat. 1040 et seq., as amended; 21 U.S.C. 321-392).

Safety data

hs_code
2921309990
Signal word
Warning
Symbol(GHS)
GHS07
Hazard statements
H315-H319-H335
Precautionary statements
P261-P305+P351+P338

Chemistry & industry

Pharmacology

ATC Code · 2 items

N - Nervous system

QN - Nervous system

Pharmacodynamics · 1 item

Tranylcypromine belongs to a class of antidepressants called monoamine oxidase inhibitors (MAOIs). Tranylcypromine is a non-hydrazine monoamine oxidase inhibitor with a rapid onset of activity. MAO is an enzyme that catalyzes the oxidative deamination of a number of amines, including serotonin, norepinephrine, epinephrine, and dopamine. Two isoforms of MAO, A and B, are found in the body. MAO-A is mainly found within cells located in the periphery and catalyzes the breakdown of serotonin, norepinephrine, epinephrine, dopamine and tyramine. MAO-B acts on phenylethylamine, norepinephrine, epinephrine, dopamine and tyramine, is localized extracellularly and is found predominantly in the brain. While the mechanism of MAOIs is still unclear, it is thought that they act by increasing free serotonin and norepinephrine concentrations and/or by altering the concentrations of other amines in the CNS. It has been postulated that depression is caused by low levels of serotonin and/or norepinephrine and that increasing serotonergic and norepinephrinergic neurotransmission results in relief of depressive symptoms. MAO A inhibition is thought to be more relevant to antidepressant activity than MAO B inhibition. Selective MAO B inhibitors, such as selegiline, have no antidepressant effects.

Mechanism of Action · 6 items

Tranylcypromine irreversibly and nonselectively inhibits monoamine oxidase (MAO). Within neurons, MAO appears to regulate the levels of monoamines released upon synaptic firing. Since depression is associated with low levels of monoamines, the inhibition of MAO serves to ease depressive symptoms, as this results in an increase in the concentrations of these amines within the CNS.

RESULTS SUGGEST THAT D- & DL-TRANYLCYPROMINE HAVE DIRECT & INDIRECT ACTIONS ON TRYPTAMINERGIC NEUROTRANSMISSION.

TRANYLCYPROMINE-HCL ADMIN IP (20 MG/KG) TO RATS: INCR IN HIPPOCAMPUS & DIENCEPHALON CONCN OF 2-PHENYLETHYLAMINE & TRYPTAMINE WERE MUCH HIGHER THAN THOSE OF M- & P-TYRAMINE. THESE MAY BE INVOLVED IN CNS NEURONAL FUNCTIONING, THEREFORE COMPONENT OF TRANYLCYPROMINE ACTIVITY.

PLATELET MAO ACTIVITY MARKEDLY DECR (DL-TRANYLCYPROMINE SULFATE 10 & 20 MG ORAL): UPTAKE OF 5-HYDROXYTRYPTAMINE, DOPAMINE & METARAMINOL ONLY SLIGHTLY DECR. MAO INHIBITOR ANTIDEPRESSANT ACTIVITY PROBABLY LESS RELATED TO CATECHOLAMINE UPTAKE INHIBITION THAN OXIDASE INHIBITION

...PRODUCE IRREVERSIBLE INACTIVATION OF MAO BY FORMING STABLE COMPLEXES WITH ENZYME. ... THERE IS EVIDENCE THAT SOME MAO INHIBITORS PREVENT RELEASE OF NOREPINEPHRINE FROM NERVE ENDINGS BY NERVE IMPULSES. /MAO INHIBITORS/

... TRANYLCYPROMINE IS A POTENT BUT NOT SPECIFIC INHIBITOR OF CYP2C19.

Biological Half-Life1.5-3.2 hours in patients with normal renal and hepatic function
Metabolism/Metabolites · 2 items

Hepatic.

Hepatic. Half Life: 1.5-3.2 hours in patients with normal renal and hepatic function

FDA Pharmacological Classification · 6 items

3E3V44J4Z9

TRANYLCYPROMINE

Established Pharmacologic Class [EPC] - Monoamine Oxidase Inhibitor

Mechanisms of Action [MoA] - Monoamine Oxidase Inhibitors

Tranylcypromine is a Monoamine Oxidase Inhibitor. The mechanism of action of tranylcypromine is as a Monoamine Oxidase Inhibitor.

TRANYLCYPROMINE

Uses & manufacturing

Uses · 3 items

MEDICATION

Use (kg; approx.) in Germany (2009): >25

Primarily indicated for the treatment of clinical depression. It is generally used to remedy various types of mood and anxiety disorders, typically after a last resort only after conventional antidepressants have been tried without success. It also has some off-label uses, such as in the treatment of post-traumatic stress disorder (PTSD). [Wikipedia]

Methods of ManufacturingBurger, Yost, J Amer Chem Soc 70, 2198 (1948); Tedeschi, US patent 2,997,422 (1961 to SK & F).
Formulations/Preparations · 2 items

Parnate, Tylciprine /Sulfate/

DOSAGE FORMS--TABLETS NF: 10 MG. /SULFATE/

General Manufacturing InformationTRANYLCYPROMINE WAS WITHDRAWN FROM MARKET FOR SOME MONTHS DURING 1964, BUT AGAIN BECAME AVAIL FOR USE IN PT UNDER CLOSE MEDICAL OBSERVATION.

Applications

Uses2-Phenylcyclopropanamine is a useful reagent for the preparation of preparation of oxadiazole derivatives as fungicides.

Suppliers21 total

济南德迈医药科技有限公司18669728830 15806766175 · [email protected]
石家庄利德康医药科技有限公司15833219835
韶远科技(上海)有限公司021-50795510 4000665055 · [email protected]
上海卡洛化学有限公司21-33526724 18930996265 · [email protected]
北京华威锐科化工科技有限公司89508211 18501085097 · [email protected]

Additional notes

DefinitionChEBI: 2-phenylcyclopropan-1-amine is a member of the class of cyclopropanes carrying amino and phenyl substituents at positions 1 and 2 respectively. It is a member of cyclopropanes, a primary amine and a member of benzenes.

Related reactions

21 records

Compound notes

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CAS 155-09-9 Tranylcypromine (HCID 5530)|Huagongshe