Geranylnerol

Details

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Internal ID 13df05c7-33ca-4ac0-9385-a5b8b320b790
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name (6Z,10E)-2,6,11,15-tetramethylhexadeca-2,6,10,14-tetraen-8-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H34O/c1-16(2)9-7-11-18(5)13-14-20(21)15-19(6)12-8-10-17(3)4/h9-10,13,15,20-21H,7-8,11-12,14H2,1-6H3/b18-13+,19-15-
InChI Key WFTQJNHPQNDNQE-BUFWFCRBSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C20H34O
Molecular Weight 290.50 g/mol
Exact Mass 290.260965704 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 6.80
Atomic LogP (AlogP) 6.12
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Geranylnerol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9871 98.71%
Caco-2 + 0.9120 91.20%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Nucleus 0.3336 33.36%
OATP2B1 inhibitior - 0.8536 85.36%
OATP1B1 inhibitior + 0.9243 92.43%
OATP1B3 inhibitior + 0.9584 95.84%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.7410 74.10%
P-glycoprotein inhibitior - 0.8164 81.64%
P-glycoprotein substrate - 0.9513 95.13%
CYP3A4 substrate - 0.6264 62.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6917 69.17%
CYP3A4 inhibition - 0.9138 91.38%
CYP2C9 inhibition - 0.9022 90.22%
CYP2C19 inhibition - 0.8853 88.53%
CYP2D6 inhibition - 0.9464 94.64%
CYP1A2 inhibition - 0.7003 70.03%
CYP2C8 inhibition - 0.9615 96.15%
CYP inhibitory promiscuity - 0.7701 77.01%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.6983 69.83%
Eye corrosion - 0.6192 61.92%
Eye irritation - 0.5142 51.42%
Skin irritation + 0.7842 78.42%
Skin corrosion - 0.9686 96.86%
Ames mutagenesis - 0.7618 76.18%
Human Ether-a-go-go-Related Gene inhibition - 0.3758 37.58%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6262 62.62%
skin sensitisation + 0.9194 91.94%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.9036 90.36%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.4784 47.84%
Acute Oral Toxicity (c) III 0.8274 82.74%
Estrogen receptor binding - 0.4946 49.46%
Androgen receptor binding - 0.7752 77.52%
Thyroid receptor binding - 0.5071 50.71%
Glucocorticoid receptor binding - 0.5786 57.86%
Aromatase binding - 0.5676 56.76%
PPAR gamma + 0.6365 63.65%
Honey bee toxicity - 0.8401 84.01%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.8701 87.01%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.06% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.55% 85.14%
CHEMBL2581 P07339 Cathepsin D 90.15% 98.95%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 88.63% 93.10%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.78% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.87% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 82.72% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Helichrysum mimetes

Cross-Links

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PubChem 70359001
LOTUS LTS0067472
wikiData Q105304202