OP(O)(O)=O.OP(O)(O)=O.COC1=C(OC)C=C2C(NC3=C2CCN2C[C@H]4[C@H](C)OC=C([C@H]4C[C@H]32)C(=O)NN)=C1

InChIKey=QLYJFIBDBMTFOF-BLBPTFAYSA-N

C22H34N4O12P2

608.478

Organic compounds

Alkaloids and derivatives

Yohimbine alkaloids

Not available

Not available

Yohimbine alkaloids

Corynanthean-type alkaloids Beta carbolines 3-alkylindoles Anisoles Alkyl aryl ethers Aralkylamines Piperidines Organic phosphoric acids and derivatives Heteroaromatic compounds Pyrroles Vinylogous esters Carboxylic acid hydrazides Trialkylamines Amino acids and derivatives Azacyclic compounds Oxacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

18-oxayohimban - Corynanthean skeleton - Yohimbine alkaloid - Beta-carboline - Pyridoindole - 3-alkylindole - Indole - Indole or derivatives - Phenol ether - Anisole - Aralkylamine - Alkyl aryl ether - Organic phosphoric acid derivative - Benzenoid - Piperidine - Vinylogous ester - Heteroaromatic compound - Pyrrole - Carboxylic acid hydrazide - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Oxacycle - Azacycle - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Carbonyl group - Organooxygen compound - Amine - Organic oxygen compound - Organic oxide - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as yohimbine alkaloids. These are alkaloids containing the pentacyclic yohimban skeleton. The Yohimbinoid alkaloids contain a carbocyclic ring E arising through C-17 to C-18 bond formation in a corynantheine precursor.

Not available