Caryophylla-4(14),8(15)-dien-5a-ol

Details

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Internal ID 11ab4bea-3b6c-450f-9247-23da787776d2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S)-6,6-dimethyl-2,9-dimethylidenecycloundecan-1-ol
SMILES (Canonical) CC1(CCCC(=C)C(CCC(=C)CC1)O)C
SMILES (Isomeric) CC1(CCCC(=C)[C@H](CCC(=C)CC1)O)C
InChI InChI=1S/C15H26O/c1-12-7-8-14(16)13(2)6-5-10-15(3,4)11-9-12/h14,16H,1-2,5-11H2,3-4H3/t14-/m0/s1
InChI Key MRNBNSIHBSPJFJ-AWEZNQCLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.23
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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Caryophylla-4(14),8(15)-dien-5.alpha.-ol

2D Structure

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2D Structure of Caryophylla-4(14),8(15)-dien-5a-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 + 0.8641 86.41%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.4667 46.67%
OATP2B1 inhibitior - 0.8464 84.64%
OATP1B1 inhibitior + 0.9240 92.40%
OATP1B3 inhibitior + 0.9073 90.73%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.8364 83.64%
P-glycoprotein inhibitior - 0.9120 91.20%
P-glycoprotein substrate - 0.9124 91.24%
CYP3A4 substrate - 0.5233 52.33%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.7416 74.16%
CYP3A4 inhibition - 0.8589 85.89%
CYP2C9 inhibition - 0.8244 82.44%
CYP2C19 inhibition - 0.7455 74.55%
CYP2D6 inhibition - 0.9392 93.92%
CYP1A2 inhibition - 0.7531 75.31%
CYP2C8 inhibition - 0.9148 91.48%
CYP inhibitory promiscuity - 0.8717 87.17%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8228 82.28%
Carcinogenicity (trinary) Non-required 0.6052 60.52%
Eye corrosion - 0.9373 93.73%
Eye irritation + 0.8474 84.74%
Skin irritation + 0.6730 67.30%
Skin corrosion - 0.9341 93.41%
Ames mutagenesis - 0.8664 86.64%
Human Ether-a-go-go-Related Gene inhibition - 0.5231 52.31%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5335 53.35%
skin sensitisation + 0.7796 77.96%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.5419 54.19%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.5563 55.63%
Acute Oral Toxicity (c) III 0.7847 78.47%
Estrogen receptor binding - 0.8070 80.70%
Androgen receptor binding - 0.7115 71.15%
Thyroid receptor binding - 0.6850 68.50%
Glucocorticoid receptor binding - 0.5779 57.79%
Aromatase binding - 0.7334 73.34%
PPAR gamma - 0.8083 80.83%
Honey bee toxicity - 0.9445 94.45%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9772 97.72%

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 92.68% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.62% 92.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.31% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.81% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.65% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.38% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.09% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 85.81% 95.93%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.41% 95.89%
CHEMBL2581 P07339 Cathepsin D 82.53% 98.95%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.79% 93.03%
CHEMBL1977 P11473 Vitamin D receptor 81.01% 99.43%
CHEMBL230 P35354 Cyclooxygenase-2 80.10% 89.63%

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.
Teucrium pseudoscorodonia
Zingiber officinale

Cross-Links

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PubChem 6429047
NPASS NPC198931
LOTUS LTS0001325
wikiData Q105170731