L-indospicine (CHEBI:6253)

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ChEBI Name	L-indospicine

ChEBI ID	CHEBI:6253

ChEBI ASCII Name	L-indospicine

Definition	An α-amino acid that is 2,7-diaminoheptanoic acid substituted by a imino group at position 7 (the 2S stereoisomer).

Stars	This entity has been manually annotated by the ChEBI Team.

Supplier Information

Download	Molfile XML SDF

Formula

C7H15N3O2

Net Charge

Average Mass

173.21290

Monoisotopic Mass

173.11643

InChI

InChI=1S/C7H15N3O2/c8-5(7(11)12)3-1-2-4-6(9)10/h5H,1-4,8H2,(H3,9,10)(H,11,12)/t5-/m0/s1

InChIKey

SILQDLDAWPQMEL-YFKPBYRVSA-N

SMILES

N[C@@H](CCCCC(N)=N)C(O)=O

Roles Classification
Chemical Role(s):	Bronsted base A molecular entity capable of accepting a hydron from a donor (Bronsted acid). (via organic amino compound ) Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Bronsted base). (via oxoacid )

Biological Role(s):	hepatotoxic agent A role played by a chemical compound exihibiting itself through the ability to induce damage to the liver in animals. plant metabolite Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.

ChEBI Ontology
Outgoing	L-indospicine (CHEBI:6253) has role hepatotoxic agent (CHEBI:50908) L-indospicine (CHEBI:6253) has role plant metabolite (CHEBI:76924) L-indospicine (CHEBI:6253) is a carboxamidine (CHEBI:35359) L-indospicine (CHEBI:6253) is a non-proteinogenic L-α-amino acid (CHEBI:83822)

IUPAC Name

(2S)-2,7-diamino-7-iminoheptanoic acid

Synonym	Source
Indospicine	KEGG COMPOUND

Last Modified

26 March 2015