Asperterpenol A

Details

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Internal ID af68e636-955e-431a-9433-f64f1516c6a8
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name (1S,2R,3S,4S,11S,12S,17S)-1,4,8,14,14,17-hexamethyltetracyclo[9.8.0.03,7.012,17]nonadec-7-en-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H42O/c1-16-8-10-19-20-15-23(3,4)11-12-24(20,5)13-14-25(19,6)22(26)21-17(2)7-9-18(16)21/h17,19-22,26H,7-15H2,1-6H3/t17-,19-,20-,21-,22+,24-,25-/m0/s1
InChI Key AKSFJIXKSLGFLQ-HZECCONOSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C25H42O
Molecular Weight 358.60 g/mol
Exact Mass 358.323565959 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 7.00
Atomic LogP (AlogP) 6.75
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Asperterpenol A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 + 0.7269 72.69%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.5078 50.78%
OATP2B1 inhibitior - 0.8640 86.40%
OATP1B1 inhibitior + 0.9068 90.68%
OATP1B3 inhibitior + 0.9015 90.15%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.7161 71.61%
P-glycoprotein inhibitior - 0.7183 71.83%
P-glycoprotein substrate - 0.7760 77.60%
CYP3A4 substrate + 0.6153 61.53%
CYP2C9 substrate - 0.6165 61.65%
CYP2D6 substrate - 0.7040 70.40%
CYP3A4 inhibition - 0.8539 85.39%
CYP2C9 inhibition - 0.6715 67.15%
CYP2C19 inhibition - 0.6039 60.39%
CYP2D6 inhibition - 0.9331 93.31%
CYP1A2 inhibition - 0.7351 73.51%
CYP2C8 inhibition - 0.7527 75.27%
CYP inhibitory promiscuity - 0.5445 54.45%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5417 54.17%
Eye corrosion - 0.9851 98.51%
Eye irritation - 0.8596 85.96%
Skin irritation + 0.6140 61.40%
Skin corrosion - 0.9446 94.46%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5934 59.34%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6699 66.99%
skin sensitisation + 0.6490 64.90%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7154 71.54%
Acute Oral Toxicity (c) III 0.6547 65.47%
Estrogen receptor binding + 0.9136 91.36%
Androgen receptor binding + 0.6574 65.74%
Thyroid receptor binding + 0.7379 73.79%
Glucocorticoid receptor binding + 0.8916 89.16%
Aromatase binding + 0.6196 61.96%
PPAR gamma + 0.5385 53.85%
Honey bee toxicity - 0.8826 88.26%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9966 99.66%

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
CHEMBL221 P23219 Cyclooxygenase-1 94.33% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.29% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.91% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.22% 97.09%
CHEMBL1871 P10275 Androgen Receptor 88.75% 96.43%
CHEMBL226 P30542 Adenosine A1 receptor 87.49% 95.93%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.16% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.81% 92.94%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 86.05% 94.78%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.13% 97.25%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 84.19% 96.38%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 83.76% 95.58%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.16% 95.89%
CHEMBL259 P32245 Melanocortin receptor 4 81.25% 95.38%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.00% 94.45%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139585311
LOTUS LTS0049382
wikiData Q77420019