Subergorgiol

Details

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Internal ID da18792a-052e-4ec1-8b2f-3654baf69bc1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Triquinane sesquiterpenoids > Angular triquinanes
IUPAC Name [(1S,2S,5R,8R,9S)-2,5,9-trimethyl-3-tricyclo[6.3.0.01,5]undec-3-enyl]methanol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-10-4-7-15-11(2)12(9-16)8-14(15,3)6-5-13(10)15/h8,10-11,13,16H,4-7,9H2,1-3H3/t10-,11+,13+,14+,15+/m0/s1
InChI Key GJNXTRPTZOVADS-PWRGDLIESA-N
Popularity 3 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 3.60
Atomic LogP (AlogP) 3.39
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEMBL526710
[(1S,2S,5R,8R,9S)-2,5,9-trimethyl-3-tricyclo[6.3.0.01,5]undec-3-enyl]methanol

2D Structure

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2D Structure of Subergorgiol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.8343 83.43%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.8417 84.17%
OATP2B1 inhibitior - 0.8509 85.09%
OATP1B1 inhibitior + 0.9298 92.98%
OATP1B3 inhibitior + 0.8741 87.41%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8395 83.95%
P-glycoprotein inhibitior - 0.9259 92.59%
P-glycoprotein substrate - 0.6997 69.97%
CYP3A4 substrate + 0.5704 57.04%
CYP2C9 substrate - 0.6015 60.15%
CYP2D6 substrate - 0.7352 73.52%
CYP3A4 inhibition - 0.8112 81.12%
CYP2C9 inhibition - 0.8377 83.77%
CYP2C19 inhibition - 0.8424 84.24%
CYP2D6 inhibition - 0.9234 92.34%
CYP1A2 inhibition - 0.8022 80.22%
CYP2C8 inhibition - 0.7106 71.06%
CYP inhibitory promiscuity - 0.7496 74.96%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.5894 58.94%
Eye corrosion - 0.9246 92.46%
Eye irritation - 0.8233 82.33%
Skin irritation - 0.5488 54.88%
Skin corrosion - 0.9685 96.85%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5257 52.57%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5016 50.16%
skin sensitisation + 0.6518 65.18%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.8323 83.23%
Acute Oral Toxicity (c) III 0.8400 84.00%
Estrogen receptor binding - 0.8525 85.25%
Androgen receptor binding + 0.6993 69.93%
Thyroid receptor binding - 0.5986 59.86%
Glucocorticoid receptor binding - 0.6896 68.96%
Aromatase binding - 0.7344 73.44%
PPAR gamma - 0.8432 84.32%
Honey bee toxicity - 0.9465 94.65%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9708 97.08%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.38% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.70% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.21% 97.25%
CHEMBL226 P30542 Adenosine A1 receptor 90.48% 95.93%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.65% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.74% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 84.29% 97.79%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.07% 82.69%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.99% 92.94%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.71% 90.24%

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.
There are no matching plants.

Cross-Links

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PubChem 636436
LOTUS LTS0051091
wikiData Q105009496