14-Hydroxy-9-epi-(E)-caryophyllene

Details

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Internal ID d619ea6e-3c32-4480-8a0b-452908804829
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name [(5Z)-6,10-dimethyl-2-methylidene-10-bicyclo[7.2.0]undec-5-enyl]methanol
SMILES (Canonical) CC1=CCCC(=C)C2CC(C2CC1)(C)CO
SMILES (Isomeric) C/C/1=C/CCC(=C)C2CC(C2CC1)(C)CO
InChI InChI=1S/C15H24O/c1-11-5-4-6-12(2)13-9-15(3,10-16)14(13)8-7-11/h5,13-14,16H,2,4,6-10H2,1,3H3/b11-5-
InChI Key DFMBJBXEHZSTJQ-WZUFQYTHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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14-Hydroxy-1-epi-caryophyllene
14-Hydroxy-9-epi-.beta.-Caryophyllene
14-Hydroxycaryophyllene
DFMBJBXEHZSTJQ-WZUFQYTHSA-N
Q67879566

2D Structure

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2D Structure of 14-Hydroxy-9-epi-(E)-caryophyllene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9881 98.81%
Caco-2 + 0.8608 86.08%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.8251 82.51%
OATP2B1 inhibitior - 0.8502 85.02%
OATP1B1 inhibitior + 0.9217 92.17%
OATP1B3 inhibitior + 0.9324 93.24%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.6313 63.13%
P-glycoprotein inhibitior - 0.9417 94.17%
P-glycoprotein substrate - 0.8990 89.90%
CYP3A4 substrate + 0.5461 54.61%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate - 0.7388 73.88%
CYP3A4 inhibition - 0.5997 59.97%
CYP2C9 inhibition - 0.6047 60.47%
CYP2C19 inhibition - 0.6767 67.67%
CYP2D6 inhibition - 0.8950 89.50%
CYP1A2 inhibition - 0.7210 72.10%
CYP2C8 inhibition - 0.5808 58.08%
CYP inhibitory promiscuity - 0.8367 83.67%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.5989 59.89%
Eye corrosion - 0.8837 88.37%
Eye irritation - 0.7099 70.99%
Skin irritation - 0.7104 71.04%
Skin corrosion - 0.9680 96.80%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3888 38.88%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.7246 72.46%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6578 65.78%
Acute Oral Toxicity (c) III 0.6645 66.45%
Estrogen receptor binding - 0.8202 82.02%
Androgen receptor binding - 0.5503 55.03%
Thyroid receptor binding - 0.7495 74.95%
Glucocorticoid receptor binding + 0.5662 56.62%
Aromatase binding - 0.6902 69.02%
PPAR gamma - 0.7512 75.12%
Honey bee toxicity - 0.9330 93.30%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9843 98.43%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.15% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.92% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.57% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.70% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.62% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.94% 95.56%
CHEMBL2996 Q05655 Protein kinase C delta 83.19% 97.79%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.61% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.06% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.04% 95.89%

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.
Daucus carota
Lindera aggregata

Cross-Links

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PubChem 5352484
NPASS NPC267285
LOTUS LTS0005304
wikiData Q67879566