Cadina-1,4-diene-3-ol

Details

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Internal ID 121d36d9-c91d-41e8-af42-61ff0ec48d97
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3,8-dimethyl-5-propan-2-yl-2,4a,5,6,7,8-hexahydronaphthalen-2-ol
SMILES (Canonical) CC1CCC(C2C1=CC(C(=C2)C)O)C(C)C
SMILES (Isomeric) CC1CCC(C2C1=CC(C(=C2)C)O)C(C)C
InChI InChI=1S/C15H24O/c1-9(2)12-6-5-10(3)13-8-15(16)11(4)7-14(12)13/h7-10,12,14-16H,5-6H2,1-4H3
InChI Key PDDMWQFBZZFOQR-UHFFFAOYSA-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 3.40
Atomic LogP (AlogP) 3.55
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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Cadina-1,4-dien-3-ol
PDDMWQFBZZFOQR-UHFFFAOYSA-N

2D Structure

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2D Structure of Cadina-1,4-diene-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7882 78.82%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.3895 38.95%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9123 91.23%
OATP1B3 inhibitior + 0.9488 94.88%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9636 96.36%
P-glycoprotein inhibitior - 0.9442 94.42%
P-glycoprotein substrate - 0.8146 81.46%
CYP3A4 substrate - 0.5700 57.00%
CYP2C9 substrate - 0.6284 62.84%
CYP2D6 substrate + 0.3479 34.79%
CYP3A4 inhibition - 0.9149 91.49%
CYP2C9 inhibition - 0.7809 78.09%
CYP2C19 inhibition - 0.7132 71.32%
CYP2D6 inhibition - 0.8494 84.94%
CYP1A2 inhibition + 0.5446 54.46%
CYP2C8 inhibition - 0.9563 95.63%
CYP inhibitory promiscuity - 0.5861 58.61%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9210 92.10%
Carcinogenicity (trinary) Non-required 0.5270 52.70%
Eye corrosion - 0.9639 96.39%
Eye irritation - 0.9087 90.87%
Skin irritation + 0.5885 58.85%
Skin corrosion - 0.8408 84.08%
Ames mutagenesis - 0.8017 80.17%
Human Ether-a-go-go-Related Gene inhibition - 0.4772 47.72%
Micronuclear - 0.9441 94.41%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation + 0.7927 79.27%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.7904 79.04%
Acute Oral Toxicity (c) III 0.7456 74.56%
Estrogen receptor binding - 0.8354 83.54%
Androgen receptor binding - 0.6207 62.07%
Thyroid receptor binding - 0.5325 53.25%
Glucocorticoid receptor binding - 0.7297 72.97%
Aromatase binding - 0.8806 88.06%
PPAR gamma - 0.8550 85.50%
Honey bee toxicity - 0.9415 94.15%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9758 97.58%

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
CHEMBL2581 P07339 Cathepsin D 91.68% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.80% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.68% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.37% 97.25%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.97% 86.00%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 81.87% 97.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.75% 95.89%
CHEMBL1871 P10275 Androgen Receptor 80.48% 96.43%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.19% 91.11%

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.
Hypericum perforatum

Cross-Links

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PubChem 6431196
NPASS NPC230616