About: geranylgeraniol

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

group of cis/trans isomers

Attributes	Values
rdf:type	Item
description	group of cis/trans isomers (en) groupe de composés cis/trans (fr)
rdfs:label	geranylgeraniol (en)
skos:prefLabel	geranylgeraniol (en)
name	geranylgeraniol (en)
IEDB Epitope ID	wds:Q27109835-81191F76-3ED1-4994-9159-0094C8BC4C4B
IEDB Epitope ID	969007
chemical structure	wds:Q27109835-4f7ccf19-423a-528f-35b0-9ce654efa3fa
chemical structure
instance of	wds:Q27109835-ce4d15db-4b89-d7c1-f38f-f1bf4b98758b
instance of	group of isomeric entities
subclass of	wds:Q27109835-1408B3DB-CDA1-42DD-A11B-49DB2A7E04E4 wds:Q27109835-534AF8AF-8A86-4576-855B-27151765EFFE
subclass of	fatty alcohol phytane diterpenoid
found in taxon	wds:Q27109835-406A2D9D-E023-419A-A60D-2B8DA856D605 wds:Q27109835-48C9D997-B018-4768-A4C1-2361D4785E54 wds:Q27109835-818DB834-57C5-43A8-84EC-C7824BC2C25A wds:Q27109835-96697CF6-23C4-46D5-8D21-D7300514A83D wds:Q27109835-D9F77F46-19F7-454D-9EAB-FDEB632B3EC4 wds:Q27109835-DEB9EF01-F604-4135-AE23-17F8BD9C79B5 wds:Q27109835-FB8DCC82-F4E5-449E-B6B2-ED422668632F
found in taxon	Pellia epiphylla Bixa orellana Bellardia trixago Cystoseira crinita Helichrysum mimetes Bifurcaria bifurcata Mikania goyazensis
UniChem compound ID	wds:Q27109835-4A0E412A-62E3-44AA-8CD7-2087EF03F191
Reaxys registry number	wds:Q27109835-4A18F704-0796-4CEC-923D-F64CDB6BB9BA
CAS Registry Number	wds:Q27109835-46FC0CC8-25B0-4040-B1EA-BCCEC0512F66
canonical SMILES	wds:Q27109835-A5BD36E6-9169-45FD-9488-7075AB48F9B8
InChI	wds:Q27109835-0399DF4A-8D4B-4E82-BDCB-56212C110104
InChIKey	wds:Q27109835-D040E400-470B-4110-BA48-4E358AEB91C4
chemical formula	wds:Q27109835-C7360C3D-773A-497E-B94D-25C1FA6B8324
ChemSpider ID	wds:Q27109835-573B07E1-1841-4F06-9C9D-FEA773651EE0
PubChem CID	wds:Q27109835-737C13F8-D418-4E8E-9064-227D08C0DCC0
ChEBI ID	wds:Q27109835-E68431A3-5037-4BB5-AE3B-5572024700A8
ChemSpider ID	http://rdf.chemspider.com/58682
PubChem CID	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID65183
ChEBI ID	http://purl.obolibrary.org/obo/CHEBI_24229
UniChem compound ID	1104332
Reaxys registry number	1797446
CAS Registry Number	7614-21-3
canonical SMILES	CC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C
InChI	InChI=1S/C20H34O/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-21/h9,11,13,15,21H,6-8,10,12,14,16H2,1-5H3
InChIKey	OJISWRZIEWCUBN-UHFFFAOYSA-N
chemical formula	C₂₀H₃₄O
ChemSpider ID	58682
PubChem CID	65183
ChEBI ID	24229
mass	wds:Q27109835-CA73FDA8-EDE5-462D-9126-2E0643B1A0C9
mass	290.261 (xsd:decimal)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q27109835
is main subject of	Dramatic variation in diterpenoids of different populations of Bellardia trixago Phloroglucinol derivatives and other constituents from South African Helichrysum species Terpenoid constituents of Pellia epiphylla A geranylacetone derivative from the brown alga Cystoseira crinita Terpenoids and an apocarotenoid from seeds of Bixa orellana (S)-12-hydroxygeranylgeraniol-derived diterpenes from the brown alga Bifurcaria bifurcata. Polar acyclic diterpenoids from Bifurcaria bifurcata (Fucales, Phaeophyta). Geranylgeraniol and geranylgeraniol-derived diterpenes from the brown alga Bifurcaria bifurcata (Cystoseiraceae) Geranylgeraniol-derived diterpenoids from the brown alga Bifurcaria bifurcata Rapid identification of cysteine-linked isoprenyl groups by metabolic labeling with [3H]farnesol and [3H]geranylgeraniol Novel farnesol and geranylgeraniol analogues: A potential new class of anticancer agents directed against protein prenylation Inhibition of neuronal cholesterol biosynthesis with lovastatin leads to impaired synaptic vesicle release even in the presence of lipoproteins or geranylgeraniol Zinc ions prevent processing of caspase-3 during apoptosis induced by geranylgeraniol in HL-60 cells. BIOSYNTHESIS OF GIBBERELLINS. I. THE BIOSYNTHESIS OF (-)-KAUREN-19-OL, AND TRANS-GERANYLGERANIOL IN ENDOSPERM NUCELLUS OF ECHINOCYSTIS MACROCARPA GREENE Enzymatic cyclization reactions of geraniol, farnesol and geranylgeraniol, and those of truncated squalene analogs having C20 and C25 by recombinant squalene cyclase Alendronate mechanism of action: geranylgeraniol, an intermediate in the mevalonate pathway, prevents inhibition of osteoclast formation, bone resorption, and kinase activation in vitro Insig-dependent ubiquitination and degradation of mammalian 3-hydroxy-3-methylglutaryl-CoA reductase stimulated by sterols and geranylgeraniol Brain cholesterol turnover required for geranylgeraniol production and learning in mice Geranylgeraniol suppresses the viability of human DU145 prostate carcinoma cells and the level of HMG CoA reductase Mevalonate depletion mediates the suppressive impact of geranylgeraniol on murine B16 melanoma cells Farnesol and geranylgeraniol: prevention and reversion of lovastatin-induced effects in NIH3T3 cells Geranylgeraniol, an intermediate product in mevalonate pathway, induces apoptotic cell death in human hepatoma cells: death receptor-independent activation of caspase-8 with down-regulation of Bcl-xL expression Geranylgeraniol and beta-ionone inhibit hepatic preneoplastic lesions, cell proliferation, total plasma cholesterol and DNA damage during the initial phases of hepatocarcinogenesis, but only the former inhibits NF-kappaB activation. Farnesol and geranylgeraniol induce actin cytoskeleton disorganization and apoptosis in A549 lung adenocarcinoma cells Geranylgeraniol is a potent inducer of apoptosis in tumor cells The mechanism of geranylgeraniol-induced apoptosis involves activation, by a caspase-3-like protease, of a c-jun N-terminal kinase signaling cascade and differs from mechanisms of apoptosis induced by conventional chemotherapeutic drugs Geranylgeraniol potently induces caspase-3-like activity during apoptosis in human leukemia U937 cells Activation of protein kinase C prevents induction of apoptosis by geranylgeraniol in human leukemia HL60 cells Farnesol and geranylgeraniol prevent activation of caspases by aminobisphosphonates: biochemical evidence for two distinct pharmacological classes of bisphosphonate drugs Geranylgeraniol overcomes the block of cell proliferation by lovastatin in C6 glioma cells. Competitive inhibition of choline phosphotransferase by geranylgeraniol and farnesol inhibits phosphatidylcholine synthesis and induces apoptosis in human lung adenocarcinoma A549 cells Biphasic requirement for geranylgeraniol in hippocampal long-term potentiation Novel salvage pathway utilizing farnesol and geranylgeraniol for protein isoprenylation Geranylgeraniol regulates negatively caspase-1 autoprocessing: implication in the Th1 response against Mycobacterium tuberculosis Lovastatin-induced apoptosis is modulated by geranylgeraniol in a neuroblastoma cell line Vitamin K(2) selectively induced apoptosis in ovarian TYK-nu and pancreatic MIA PaCa-2 cells out of eight solid tumor cell lines through a mechanism different from geranylgeraniol Production of geranylgeraniol on overexpression of a prenyl diphosphate synthase fusion gene in Saccharomyces cerevisiae Overproduction of geranylgeraniol by metabolically engineered Saccharomyces cerevisiae Biphasic effects of geranylgeraniol, teprenone, and phytol on the growth of Staphylococcus aureus Phytol synthesis from geranylgeraniol in spinach chloroplasts Roles of rat and human aldo-keto reductases in metabolism of farnesol and geranylgeraniol A novel 21-kDa cytochrome c-releasing factor is generated upon treatment of human leukemia U937 cells with geranylgeraniol Hydrogenation of geranylgeraniol : two pathways exist in spinach chloroplasts Site of synthesis of geranylgeraniol derivatives in intact spinach chloroplasts

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