Coprine
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Category | Mycotoxins |
Catalog number | BBF-01054 |
CAS | 58919-61-2 |
Molecular Weight | 202.21 |
Molecular Formula | C8H14N2O4 |
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Description
It is produced by the strain of Coprinus atramentarius. It can affect the liver to degrade ethanol.
Specification
Synonyms | N-(1-hydroxycyclopropyl)-L-glutamine; N(5)-(1-Hydroxycyclopropyl)-L-glutamine |
IUPAC Name | (2S)-2-amino-5-[(1-hydroxycyclopropyl)amino]-5-oxopentanoic acid |
Canonical SMILES | C1CC1(NC(=O)CCC(C(=O)O)N)O |
InChI | InChI=1S/C8H14N2O4/c9-5(7(12)13)1-2-6(11)10-8(14)3-4-8/h5,14H,1-4,9H2,(H,10,11)(H,12,13)/t5-/m0/s1 |
InChI Key | OEEZRBUCLFMTLD-YFKPBYRVSA-N |
Source | Coprine occurs naturally in the otherwise edible mushroom, the common ink cap (Coprinopsis atramentaria). |
Properties
Appearance | White Crystal |
Melting Point | 197-199 °C |
Solubility | Soluble in Water |
Toxicity
Carcinogenicity | No indication of carcinogenicity to humans (not listed by IARC). |
Mechanism Of Toxicity | It metabolises to 1-aminocyclopropanol, a closely-related chemical to Disulfiram and exhibits the same mechanism of action: inhibition of the enzyme acetaldehyde dehydrogenase, which is required for alchohol metabolism. |
Reference Reading
Spectrum
Predicted LC-MS/MS Spectrum - 10V, Positive
Experimental Conditions
Collision Energy: 10 eV
Instrument Type: QTOF (generic), spectrum predicted by CFM-ID
Mass Resolution: 0.0001 Da
1H NMR Spectrum
Experimental Conditions
Nucleus: 1H
Frequency: 100
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Bio Calculators
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2