(+)-9-Hydroxyselina-4,11-diene

Details

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Internal ID 57aa6be4-a603-4a6c-b1ff-ae997aecc252
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name 5,8a-dimethyl-3-prop-1-en-2-yl-2,3,4,6,7,8-hexahydro-1H-naphthalen-1-ol
SMILES (Canonical) CC1=C2CC(CC(C2(CCC1)C)O)C(=C)C
SMILES (Isomeric) CC1=C2CC(CC(C2(CCC1)C)O)C(=C)C
InChI InChI=1S/C15H24O/c1-10(2)12-8-13-11(3)6-5-7-15(13,4)14(16)9-12/h12,14,16H,1,5-9H2,2-4H3
InChI Key IKGXPRLTFOMFQV-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) 3.84
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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IKGXPRLTFOMFQV-UHFFFAOYSA-N

2D Structure

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2D Structure of (+)-9-Hydroxyselina-4,11-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.8531 85.31%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.5237 52.37%
OATP2B1 inhibitior - 0.8476 84.76%
OATP1B1 inhibitior + 0.8733 87.33%
OATP1B3 inhibitior + 0.9155 91.55%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.8043 80.43%
P-glycoprotein inhibitior - 0.9273 92.73%
P-glycoprotein substrate - 0.8488 84.88%
CYP3A4 substrate + 0.5567 55.67%
CYP2C9 substrate - 0.6499 64.99%
CYP2D6 substrate - 0.6843 68.43%
CYP3A4 inhibition - 0.7847 78.47%
CYP2C9 inhibition - 0.7275 72.75%
CYP2C19 inhibition - 0.5964 59.64%
CYP2D6 inhibition - 0.9384 93.84%
CYP1A2 inhibition - 0.8085 80.85%
CYP2C8 inhibition - 0.8390 83.90%
CYP inhibitory promiscuity - 0.8476 84.76%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5504 55.04%
Eye corrosion - 0.9850 98.50%
Eye irritation + 0.8071 80.71%
Skin irritation + 0.6376 63.76%
Skin corrosion - 0.9380 93.80%
Ames mutagenesis - 0.8542 85.42%
Human Ether-a-go-go-Related Gene inhibition - 0.4646 46.46%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5607 56.07%
skin sensitisation + 0.5496 54.96%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.5599 55.99%
Acute Oral Toxicity (c) III 0.8426 84.26%
Estrogen receptor binding - 0.8554 85.54%
Androgen receptor binding - 0.5761 57.61%
Thyroid receptor binding - 0.6775 67.75%
Glucocorticoid receptor binding - 0.7773 77.73%
Aromatase binding - 0.6064 60.64%
PPAR gamma - 0.7798 77.98%
Honey bee toxicity - 0.7960 79.60%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9917 99.17%

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 93.66% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 90.36% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.68% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.44% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.00% 100.00%
CHEMBL2581 P07339 Cathepsin D 83.48% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.19% 97.09%
CHEMBL1951 P21397 Monoamine oxidase A 82.86% 91.49%
CHEMBL2996 Q05655 Protein kinase C delta 82.65% 97.79%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.65% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.49% 95.89%
CHEMBL259 P32245 Melanocortin receptor 4 80.83% 95.38%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.15% 82.69%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.14% 96.95%

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.
Marsupella aquatica

Cross-Links

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PubChem 5319684
LOTUS LTS0021772
wikiData Q105114600