About: (-)-(R)-19-hydroxytabersonine(1+)

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About: (-)-(R)-19-hydroxytabersonine(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	(-)-(R)-19-hydroxytabersonine(1+) (en)
skos:prefLabel	(-)-(R)-19-hydroxytabersonine(1+) (en)
name	(-)-(R)-19-hydroxytabersonine(1+) (en)
isomeric SMILES	wds:Q74411545-C6C0753C-7AC4-4DE0-9A9D-60F1CF5E75B4
isomeric SMILES	C[C@H]([C@]12CC(=C3[C@@]4([C@H]1[NH+](CC4)CC=C2)C5=CC=CC=C5N3)C(=O)OC)O
instance of	wds:Q74411545-6BDB2A9A-D553-4932-AF3B-4E60C16DB0B6
instance of	type of chemical entity
subclass of	wds:Q74411545-8A956F6B-F428-4D28-8881-590EB16B748A wds:Q74411545-B361BCD8-B0B7-4A04-BCCB-6AA9031EF49E
subclass of	organic cation ammonium ion derivative
UniChem compound ID	wds:Q74411545-816E2C34-E2C7-4CFD-9C26-0BA7419A4522
canonical SMILES	wds:Q74411545-837DC3A6-C1B1-4849-8B25-2FE0C2AE96EC
InChI	wds:Q74411545-F5445A39-9492-4B86-A748-23D340FE57C8
InChIKey	wds:Q74411545-15290F0B-7506-4E9B-A954-A014919ED6E6
chemical formula	wds:Q74411545-47ACE946-DFF5-472A-8DFB-AB1CF1A6BD98
PubChem CID	wds:Q74411545-460C18BC-426E-421C-9756-55198791F22C
ChEBI ID	wds:Q74411545-F61A38F7-8334-4F91-8781-CA921139BB10
PubChem CID	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID138911113
ChEBI ID	http://purl.obolibrary.org/obo/CHEBI_144372
UniChem compound ID	170274333
canonical SMILES	COC(=O)C1=C2Nc3ccccc3C23CC[NH+]2CC=CC(C(C)O)(C1)C23
InChI	InChI=1S/C21H24N2O3/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/h3-8,13,19,22,24H,9-12H2,1-2H3/p+1/t13-,19+,20+,21+/m1/s1
InChIKey	XDGRXQNYJMQLPU-VLCNGCBASA-O
chemical formula	C₂₁H₂₅N₂O₃⁺
PubChem CID	138911113
ChEBI ID	144372
mass	wds:Q74411545-3E5BCE3E-2902-4257-9A81-4B6BD7884EF2
mass	353.18596908008993 (xsd:decimal)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74411545
is main subject of	A stereoselective hydroxylation step of alkaloid biosynthesis by a unique cytochrome P450 in Catharanthus roseus The assembly of (+)-vincadifformine- and (-)-tabersonine-derived monoterpenoid indole alkaloids in Catharanthus roseus involves separate branch pathways
is main subject of	wds:Q34947534-5C6EB863-01AA-4C31-B6F9-CD5E9062BB84 wds:Q90145756-9A848E25-FAF5-43BE-9ACA-BA2CEA499550

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