About: 4-(3-hydroxyprop-1-en-1-yl)-2-methoxyphenol

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About: 4-(3-hydroxyprop-1-en-1-yl)-2-methoxyphenol Goto Sponge NotDistinct Permalink

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

chemical compound

Attributes	Values
rdf:type	Item
description	химическое соединение (ru) chemical compound (en) composé chimique (fr) compositum chemicum (la) chemische Verbindung (de) chemische verbinding (nl) compuestu químicu (ast) хімічна сполука (uk) রাসায়নিক যৌগ (bn)
rdfs:label	4-(3-hydroxyprop-1-en-1-yl)-2-methoxyphenol (en)
skos:prefLabel	4-(3-hydroxyprop-1-en-1-yl)-2-methoxyphenol (en)
name	4-(3-hydroxyprop-1-en-1-yl)-2-methoxyphenol (en)
instance of	wds:Q104169674-728E2AC9-81F4-44F8-8F9A-2F7D10D4F779
instance of	type of chemical entity
subclass of	wds:Q104169674-8F3EB3E9-DA4C-4A5C-9558-D4AF5009C326
subclass of	chemical substance
found in taxon	wds:Q104169674-06C1312B-1D0C-4905-930D-D08D79583D59 wds:Q104169674-1370CA4C-4CD2-4468-8956-A21D8D9FC83F wds:Q104169674-187D9EF5-46E8-42D0-8870-A81CC355451B wds:Q104169674-18B0BEA8-98E6-4D28-B942-A9A630FDDEAE wds:Q104169674-2870A0C1-B825-4BA4-9E80-3E751EE52A2D wds:Q104169674-3506C7D9-C5EA-4F1C-B2A8-4ABA52D6562B wds:Q104169674-638B2027-8295-4184-BEF7-B5727BF8A14A wds:Q104169674-6BB9CF66-3401-4349-BFE6-AC43C09DFA40 wds:Q104169674-6CA4E308-BBCF-45CC-896F-86F66C98DF81 wds:Q104169674-723FDED2-F895-40E3-AF8A-232473F70B94 wds:Q104169674-7C1164EC-CC54-4F7A-A772-0298640F4A8B wds:Q104169674-7CC9D10E-FABD-4EF2-AFB0-1CE26DDD18E8 wds:Q104169674-9140DC3A-8F1E-4843-A2AE-BC45622BD093 wds:Q104169674-9BDE7AB6-5AAF-4734-8596-D93E97AC62E6 wds:Q104169674-9E42B2B5-6E4D-427A-9BB6-BC657C37BF37 wds:Q104169674-B5058B50-0D4F-426B-8D54-D00D631B52B6 wds:Q104169674-B76AC15C-3460-4545-B78C-658A18F276A5 wds:Q104169674-C7DAE57E-C5A2-461C-A08A-6C87F32C5C4A wds:Q104169674-D96C194B-6A93-475E-B6F0-FD461578FA97 wds:Q104169674-E6F39244-D752-48E6-AB1A-51968617CAE0
found in taxon	Linum flavum Broussonetia papyrifera Picea abies Paecilomyces fulvus Echinacea purpurea Fagus grandifolia Acorus gramineus Asparagus cochinchinensis Pinus strobus Magnolia officinalis Xanthium spinosum Hedyotis lawsoniae Stemona collinsae Artemisia xerophytica Helicteres angustifolia Linum album Aeschynanthus bracteatus Melanthera prostrata Oxytropis myriophylla Wollastonia dentata
UniChem compound ID	wds:Q104169674-C1E58C1C-D187-45E7-9333-C6C6CC6ECA57
CAS Registry Number	wds:Q104169674-9A87F90D-44D6-4AD7-950F-D49573DB00DD wds:Q104169674-C3C318B7-89B0-4D05-B7FB-B821F66C4AEC
canonical SMILES	wds:Q104169674-1BA3025D-C1C8-4F52-B93F-F0F8A0FE009E
InChI	wds:Q104169674-D7B94318-72E7-4AEE-AA91-0E88BF0B8952
InChIKey	wds:Q104169674-88D43C3F-653D-4C4F-80F3-3B73C245280A
chemical formula	wds:Q104169674-BCC1AF5A-4653-4953-8DA0-84F3E01D4B76
PubChem CID	wds:Q104169674-F82D949E-4549-4238-8A5A-DCC18D55844A
PubChem CID	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9983
UniChem compound ID	24661380
CAS Registry Number	458-35-5 26745-55-1
canonical SMILES	OC1=CC=C(C=CCO)C=C1OC
InChI	InChI=1S/C10H12O3/c1-13-10-7-8(3-2-6-11)4-5-9(10)12/h2-5,7,11-12H,6H2,1H3
InChIKey	JMFRWRFFLBVWSI-UHFFFAOYSA-N
chemical formula	C₁₀H₁₂O₃
PubChem CID	9983
mass	wds:Q104169674-1FE06758-037E-4AAE-9CD1-4F611742C5B6
mass	180.078644244 (xsd:decimal)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q104169674
is main subject of	Analysis of chemical changes in Picea abies wood decayed by different Streptomyces strains showing evidence for biopulping procedures Xanthanolides from Xanthium: Absolute configuration of xanthanol, isoxanthanol and their C-4 epimers Sesquiterpene lactones and other constituents from Artemisia xerophytica Accumulation of podophyllotoxin and related lignans in cell suspension cultures of linum album Aryltetralin lignans from Linum flavum and Linum capitatum Cis-monolignols in Fagus grandifolia and their possible involvement in lignification Antifungal stilbenoids from Stemona collinsae. Pregnane, coumarin and lupane derivatives and cytotoxic constituents from Helicteres angustifolia Antioxidant phenolics from Broussonetia papyrifera fruits Bioactive constituents from Asparagus cochinchinensis. Suppression of CCR impacts metabolite profile and cell wall composition in Pinus radiata tracheary elements Phenolic constituents from the stem bark of Magnolia officinalis Structure and accumulation of phenolics in elicited Echinacea purpurea cell cultures. Studies on the constituents of medicinal and related plants in Sri Lanka. III. Novel sesquilignans from Hedyotis lawsoniae. Microbial synthesis of coniferyl alcohol by the fungus Byssochlamys fulva V107 Chemical constituents of Aeschynanthus bracteatus and their weak anti-inflammatory activities. Phenolic glucosides from Oxytropis myriophylla Phenolic constituents from the rhizomes of Acorus gramineus and their biological evaluation on antitumor and anti-inflammatory activities Cinnamyl alcohols and methyl esters of fatty acids from Wedelia prostrata callus cultures
is main subject of	wds:Q43055974-10B75E8A-64F3-4F83-8AB5-D1DF1839D9D0 wds:Q45046970-20F62BF0-0420-45BE-AA1B-D876A194D263 wds:Q46195852-D0F754C2-D519-4E55-9557-D30820C0A8B2 wds:Q58645716-299C3408-884B-4505-8444-E82084E4EE35

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