alpha-Caryophylladienol

Details

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Internal ID 6785bec6-afbc-48a1-af23-2abd22d02d2b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,5R,9R)-10,10-dimethyl-2,6-dimethylidenebicyclo[7.2.0]undecan-5-ol
SMILES (Canonical) CC1(CC2C1CCC(=C)C(CCC2=C)O)C
SMILES (Isomeric) CC1(C[C@H]2[C@H]1CCC(=C)[C@@H](CCC2=C)O)C
InChI InChI=1S/C15H24O/c1-10-6-8-14(16)11(2)5-7-13-12(10)9-15(13,3)4/h12-14,16H,1-2,5-9H2,3-4H3/t12-,13-,14-/m1/s1
InChI Key CIIYOYPOMGIECX-MGPQQGTHSA-N
Popularity 4 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 3.30
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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CIIYOYPOMGIECX-MGPQQGTHSA-N
(1s,5r,9r)-10,10-dimethyl-2,6-dimethylenebicyclo[7.2.0]undecan-5-ol

2D Structure

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2D Structure of alpha-Caryophylladienol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 + 0.7643 76.43%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.5413 54.13%
OATP2B1 inhibitior - 0.8462 84.62%
OATP1B1 inhibitior + 0.9099 90.99%
OATP1B3 inhibitior + 0.9033 90.33%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9252 92.52%
P-glycoprotein inhibitior - 0.9022 90.22%
P-glycoprotein substrate - 0.9168 91.68%
CYP3A4 substrate + 0.5404 54.04%
CYP2C9 substrate - 0.6165 61.65%
CYP2D6 substrate - 0.7040 70.40%
CYP3A4 inhibition - 0.7557 75.57%
CYP2C9 inhibition - 0.7770 77.70%
CYP2C19 inhibition - 0.6590 65.90%
CYP2D6 inhibition - 0.9343 93.43%
CYP1A2 inhibition - 0.6837 68.37%
CYP2C8 inhibition - 0.8458 84.58%
CYP inhibitory promiscuity - 0.8990 89.90%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5665 56.65%
Eye corrosion - 0.9587 95.87%
Eye irritation + 0.7239 72.39%
Skin irritation + 0.6466 64.66%
Skin corrosion - 0.9285 92.85%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4309 43.09%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation + 0.6867 68.67%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6419 64.19%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.4919 49.19%
Acute Oral Toxicity (c) III 0.7748 77.48%
Estrogen receptor binding - 0.6490 64.90%
Androgen receptor binding - 0.6266 62.66%
Thyroid receptor binding - 0.6779 67.79%
Glucocorticoid receptor binding + 0.5789 57.89%
Aromatase binding - 0.7155 71.55%
PPAR gamma - 0.7501 75.01%
Honey bee toxicity - 0.9130 91.30%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9775 97.75%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.61% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.52% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.42% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.79% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.99% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.09% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 87.43% 90.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.04% 94.45%
CHEMBL226 P30542 Adenosine A1 receptor 83.69% 95.93%
CHEMBL1871 P10275 Androgen Receptor 82.87% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.76% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.22% 95.89%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 81.35% 94.78%

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.
Abies sibirica
Artemisia annua

Cross-Links

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PubChem 14524923
LOTUS LTS0065243
wikiData Q104959828