About: (+)-minovincinine(1+)

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About: (+)-minovincinine(1+) Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

cation

Attributes	Values
rdf:type	Item
description	cation (en)
rdfs:label	(+)-minovincinine(1+) (en)
skos:prefLabel	(+)-minovincinine(1+) (en)
name	(+)-minovincinine(1+) (en)
isomeric SMILES	wds:Q74417921-94AD1DBA-75F3-457D-9F44-BFD38B445CBC
isomeric SMILES	C[C@@H]([C@]12CCC[NH+]3[C@H]1[C@]4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)O
instance of	wds:Q74417921-B488738D-1F39-4571-AAE3-E92734361BC7
instance of	group of stereoisomers
subclass of	wds:Q74417921-527DD605-D61C-42C9-B6CC-B7782FAA0279 wds:Q74417921-6998D929-5469-4CF2-B898-5488D765A4B7
subclass of	organic cation ammonium ion derivative
UniChem compound ID	wds:Q74417921-273CE57A-CA56-4166-94F7-B4485842F66E
canonical SMILES	wds:Q74417921-7FF81443-1F02-4A9F-8831-49191B6DF523
InChI	wds:Q74417921-BBBEE424-833A-4370-8AC9-2D2F9A68A5AD
InChIKey	wds:Q74417921-15A53F1E-DA6A-48B2-927F-A8E172E42D47
chemical formula	wds:Q74417921-B8BE23FD-4AA3-4FEC-B986-E1A7BD3364B0
PubChem CID	wds:Q74417921-6BADCE8F-5968-4EAD-808B-687601F2CE13
ChEBI ID	wds:Q74417921-185CF167-4376-4D80-82C4-F21DA20513C5
PubChem CID	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID138911111
ChEBI ID	http://purl.obolibrary.org/obo/CHEBI_144371
UniChem compound ID	170274332
canonical SMILES	COC(=O)C1=C2Nc3ccccc3C23CC[NH+]2CCCC(C(C)O)(C1)C23
InChI	InChI=1S/C21H26N2O3/c1-13(24)20-8-5-10-23-11-9-21(19(20)23)15-6-3-4-7-16(15)22-17(21)14(12-20)18(25)26-2/h3-4,6-7,13,19,22,24H,5,8-12H2,1-2H3/p+1/t13-,19+,20+,21+/m0/s1
InChIKey	BKMGDPNQILJWLI-ODVVLEEXSA-O
chemical formula	C₂₁H₂₇N₂O₃⁺
PubChem CID	138911111
ChEBI ID	144371
mass	wds:Q74417921-A6437969-DA2B-41B0-A060-146C5F1643DC
mass	355.20161914408993 (xsd:decimal)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74417921
is main subject of	Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase A BAHD acyltransferase catalyzing 19-O-acetylation of tabersonine derivatives in roots of Catharanthus roseus enables combinatorial synthesis of monoterpene indole alkaloids. The assembly of (+)-vincadifformine- and (-)-tabersonine-derived monoterpenoid indole alkaloids in Catharanthus roseus involves separate branch pathways
is main subject of	wds:Q28345713-4A90A2A8-0D1E-43DC-9168-6C36352D37B0 wds:Q50041282-0B3F5984-D441-46A7-8D87-27AEB482017F wds:Q90145756-D3107394-B799-4495-82F0-D771CA185ECE

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