Selma-4(14),7(1 I)-dlene-9-01 (I)

Details

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Internal ID 79df7c83-e876-4602-bde8-8695d3f79a0d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 8a-methyl-5-methylidene-3-propan-2-ylidene-2,4,4a,6,7,8-hexahydro-1H-naphthalen-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-10(2)12-8-13-11(3)6-5-7-15(13,4)14(16)9-12/h13-14,16H,3,5-9H2,1-2,4H3
InChI Key KIWHFBIBAJSYHN-UHFFFAOYSA-N
Popularity 2 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) 3.84
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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8a-methyl-5-methylidene-3-propan-2-ylidene-2,4,4a,6,7,8-hexahydro-1H-naphthalen-1-ol
RefChem:182332
CHEBI:199345

2D Structure

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2D Structure of Selma-4(14),7(1 I)-dlene-9-01 (I)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.8049 80.49%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.4786 47.86%
OATP2B1 inhibitior - 0.8497 84.97%
OATP1B1 inhibitior + 0.8527 85.27%
OATP1B3 inhibitior - 0.2356 23.56%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8586 85.86%
P-glycoprotein inhibitior - 0.9108 91.08%
P-glycoprotein substrate - 0.8883 88.83%
CYP3A4 substrate + 0.5206 52.06%
CYP2C9 substrate - 0.6165 61.65%
CYP2D6 substrate - 0.7040 70.40%
CYP3A4 inhibition - 0.7718 77.18%
CYP2C9 inhibition - 0.7840 78.40%
CYP2C19 inhibition - 0.6405 64.05%
CYP2D6 inhibition - 0.9470 94.70%
CYP1A2 inhibition - 0.8472 84.72%
CYP2C8 inhibition - 0.9345 93.45%
CYP inhibitory promiscuity - 0.8140 81.40%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6118 61.18%
Eye corrosion - 0.9834 98.34%
Eye irritation + 0.8884 88.84%
Skin irritation + 0.6582 65.82%
Skin corrosion - 0.9419 94.19%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4661 46.61%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation + 0.6727 67.27%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7015 70.15%
Acute Oral Toxicity (c) III 0.8879 88.79%
Estrogen receptor binding - 0.6526 65.26%
Androgen receptor binding - 0.5551 55.51%
Thyroid receptor binding - 0.6587 65.87%
Glucocorticoid receptor binding - 0.6931 69.31%
Aromatase binding - 0.6955 69.55%
PPAR gamma - 0.7509 75.09%
Honey bee toxicity - 0.8469 84.69%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9934 99.34%

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 92.79% 91.11%
CHEMBL1977 P11473 Vitamin D receptor 91.40% 99.43%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.07% 97.25%
CHEMBL1951 P21397 Monoamine oxidase A 88.38% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.61% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.61% 100.00%
CHEMBL2581 P07339 Cathepsin D 81.49% 98.95%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.08% 95.50%

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.
Aesculus hippocastanum

Cross-Links

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PubChem 73828322
LOTUS LTS0248245
wikiData Q105232132