Phenelzine Sulfate - ≥97% , Monoamine oxidase inhibitor, CAS No.156-51-4, Monoamine oxidase inhibitor

CAS: 156-51-4 Cat. No.: P132003 Molecular Weight: 234.27 EC Number: 205-856-0 PubChem CID: 61100

GRADE & PURITY ≥97%

Synonyms

2-phenylethylhydrazine sulfate | HMS1920J08 | HY-B1018A | PHENELZINE SULFATE [MART.] | Phenylaethyl-Hydrazin | Tox21_200134 | PHENELZINE SULFATE SALT | Phenelzinesulfate | Phenethylhydrazin | S 1544 | PHENELZINE SULFATE [WHO-DD] | Phenelzine sulphate | HM

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Specifications

Synonyms

2-phenylethylhydrazine sulfate | HMS1920J08 | HY-B1018A | PHENELZINE SULFATE [MART.] | Phenylaethyl-Hydrazin | Tox21_200134 | PHENELZINE SULFATE SALT | Phenelzinesulfate | Phenethylhydrazin | S 1544 | PHENELZINE SULFATE [WHO-DD] | Phenelzine sulphate | HM

Specifications & Purity

≥97%

Biochemical and Physiological Mechanisms

Phenelzine sulfate is a non-selective and irreversible monoamine oxidase inhibitor (MAOI), used as an antidepressant and anxiolytic.

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Action Type

INHIBITOR

Mechanism of action

Monoamine oxidase inhibitor

Purity

≥97%

Names and Identifiers

• Pubchem Sid: 504753744
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504753744
• Canonical Smiles: C1=CC=C(C=C1)CCNN.OS(=O)(=O)O
• IUPAC Name: 2-phenylethylhydrazine;sulfuric acid
• InChIKey: RXBKMJIPNDOHFR-UHFFFAOYSA-N
• INCHI: 1S/C8H12N2.H2O4S/c9-10-7-6-8-4-2-1-3-5-8;1-5(2,3)4/h1-5,10H,6-7,9H2;(H2,1,2,3,4)
• Isomeric SMILES: C1=CC=C(C=C1)CCNN.OS(=O)(=O)O
• WGK Germany: 3
• RTECS: MV8750000
• PubChem CID: 61100
• Molecular Weight: 234.27

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Organic sulfuric acids and derivatives
      • Subclass Organic sulfuric acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Organic sulfuric acids and derivatives
• Subclass: Organic sulfuric acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic sulfuric acids
• Alternative Parents: Benzene and substituted derivatives Alkylhydrazines Organopnictogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Sulfuric acid - Benzenoid - Monocyclic benzene moiety - Alkylhydrazine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Hydrazine derivative - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as organic sulfuric acids. These are organic compounds containing the sulfuric acid functional group, with the generic structure HOS(=O)(=O)OH.
• External Descriptors: organic molecular entity

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

KCNH2 Tclin HERG (29587 Activities)

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GBA1 Tclin Beta-glucocerebrosidase (14647 Activities)

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GAA Tclin Lysosomal alpha-glucosidase (35701 Activities)

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ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

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CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

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TP53 Tchem Cellular tumor antigen p53 (48468 Activities)

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KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)

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EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

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KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)

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LMNA Tbio Prelamin-A/C (36751 Activities)

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BLM Tchem Bloom syndrome protein (4248 Activities)

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GMNN Tbio Geminin (128009 Activities)

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PMP22 Tbio Peripheral myelin protein 22 (699 Activities)

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microRNA 21 (64692 Activities)

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SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)

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GFER Tchem FAD-linked sulfhydryl oxidase ALR (1466 Activities)

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ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)

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MPHOSPH8 Tbio M-phase phosphoprotein 8 (656 Activities)

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SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)

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HSPA5 Tchem 78 kDa glucose-regulated protein (3319 Activities)

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RUNX1 Tbio Runt-related transcription factor 1/Core-binding factor subunit beta (7867 Activities)

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Associated Targets(non-human)

Pseudomonas aeruginosa (123386 Activities)

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Klebsiella pneumoniae (43867 Activities)

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Staphylococcus aureus (210822 Activities)

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Acinetobacter baumannii (41033 Activities)

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Escherichia coli (133304 Activities)

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Plasmodium falciparum (966862 Activities)

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Cryptococcus neoformans (21258 Activities)

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Candida albicans (78123 Activities)

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Luciferin 4-monooxygenase (66902 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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Mapt Microtubule-associated protein tau (6 Activities)

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Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

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Rorc Nuclear receptor ROR-gamma (89407 Activities)

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Mechanisms of Action

Chemical and Physical Properties

• Sensitivity: Moisture sensitive；Light sensitive
• Molecular Weight: 234.280 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• Exact Mass: 234.067 Da
• Monoisotopic Mass: 234.067 Da
• Topological Polar Surface Area: 121.000 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 159.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

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