About: hoerhammericine(1+)

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About: hoerhammericine(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	hoerhammericine(1+) (en)
skos:prefLabel	hoerhammericine(1+) (en)
name	hoerhammericine(1+) (en)
isomeric SMILES	wds:Q74410597-B4C51FA4-9A0B-464F-AB45-34C667894AA5
isomeric SMILES	C[C@H]([C@]12CC(=C3[C@@]4([C@H]1[NH+](CC4)C[C@H]5[C@@H]2O5)C6=CC=CC=C6N3)C(=O)OC)O
instance of	wds:Q74410597-962C0196-B598-486E-85D5-2E7A00E6D91A
instance of	group of stereoisomers
subclass of	wds:Q74410597-AFD3F795-8CC5-4F9A-8C67-4922D2CFD160 wds:Q74410597-F2EA16B7-6C8D-4904-8B03-C6C59E4C561E
subclass of	organic cation ammonium ion derivative
UniChem compound ID	wds:Q74410597-7F726F12-D01F-4F13-9EB1-0269F4BD1930
canonical SMILES	wds:Q74410597-B3B058FD-F810-432F-80D0-108DEA68B998
InChI	wds:Q74410597-B559915F-29C1-4147-9043-2DD5BCC783F3
InChIKey	wds:Q74410597-3253A782-8BFC-4336-AA76-81A4BB47738F
chemical formula	wds:Q74410597-D93C76A4-1985-4BEA-821F-8221BE3E01E0
PubChem CID	wds:Q74410597-CD558F62-5EAB-47FE-84BA-79483FD7EDA2
ChEBI ID	wds:Q74410597-A9572975-5008-492E-A2FC-0DB3A9BB3738
PubChem CID	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID138911116
ChEBI ID	http://purl.obolibrary.org/obo/CHEBI_144375
UniChem compound ID	170274336
canonical SMILES	COC(=O)C1=C2Nc3ccccc3C23CC[NH+]2CC4OC4C(C(C)O)(C1)C23
InChI	InChI=1S/C21H24N2O4/c1-11(24)21-9-12(18(25)26-2)16-20(13-5-3-4-6-14(13)22-16)7-8-23(19(20)21)10-15-17(21)27-15/h3-6,11,15,17,19,22,24H,7-10H2,1-2H3/p+1/t11-,15+,17+,19-,20+,21+/m1/s1
InChIKey	QVNXPWJNUKKMHP-JJGNIUBRSA-O
chemical formula	C₂₁H₂₅N₂O₄⁺
PubChem CID	138911116
ChEBI ID	144375
mass	wds:Q74410597-07889FCF-D0B0-49C5-8637-6D7C890D3210
mass	369.18088370008996 (xsd:decimal)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74410597
is main subject of	Monomeric indole alkaloids from the aerial parts of Catharanthus roseus Catharanthus alkaloids XXXII: isolation of alkaloids from Catharanthus trichophyllus roots and structure elucidation of cathaphylline A stereoselective hydroxylation step of alkaloid biosynthesis by a unique cytochrome P450 in Catharanthus roseus Effect of sodium nitroprusside on growth and terpenoid indole alkaloid production in Catharanthus roseus hairy root cultures. Effect of Geometrical Structure, Drying, and Synthetic Method on Aminated Chitosan-Coated Magnetic Nanoparticles Utility for HSA Effective Immobilization Effects of buffered media upon growth and alkaloid production of Catharanthus roseus hairy roots
is main subject of	wds:Q92164798-863C41BC-30FD-4F16-BBAE-D6CAE6EAE380 wds:Q34947534-B35933BD-648D-4909-A7F3-5D45A97F4BF7 wds:Q39543539-CEA50708-E298-4FE8-B252-4E4A8D342F59 wds:Q45003179-01736098-7668-48FF-BB9C-AB717D4A7B71 wds:Q73692261-A3A751D2-ABBA-4DA6-99EE-3474C7E1981D wds:Q42748520-CB164B43-C998-4EBA-AAEA-4C5A0313DB75

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