(1S,2S,5S,7S,10S,11S)-10-[(3R)-3-hydroperoxy-4-methylpent-4-enyl]-2,7,10-trimethyl-6-oxatricyclo[9.1.0.05,7]dodecan-2-ol

Details

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Internal ID a05d98b7-99b6-49ec-ac49-b2524ce109a9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name (1S,2S,5S,7S,10S,11S)-10-[(3R)-3-hydroperoxy-4-methylpent-4-enyl]-2,7,10-trimethyl-6-oxatricyclo[9.1.0.05,7]dodecan-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H34O4/c1-13(2)16(24-22)6-8-18(3)10-11-20(5)17(23-20)7-9-19(4,21)15-12-14(15)18/h14-17,21-22H,1,6-12H2,2-5H3/t14-,15-,16+,17-,18-,19-,20-/m0/s1
InChI Key PNSFHPGODPYTML-DSWGTCOTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H34O4
Molecular Weight 338.50 g/mol
Exact Mass 338.24570956 g/mol
Topological Polar Surface Area (TPSA) 62.20 Ų
XlogP 3.60
Atomic LogP (AlogP) 4.33
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,2S,5S,7S,10S,11S)-10-[(3R)-3-hydroperoxy-4-methylpent-4-enyl]-2,7,10-trimethyl-6-oxatricyclo[9.1.0.05,7]dodecan-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9627 96.27%
Caco-2 + 0.5713 57.13%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.4118 41.18%
OATP2B1 inhibitior - 0.8558 85.58%
OATP1B1 inhibitior + 0.9254 92.54%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8060 80.60%
P-glycoprotein inhibitior - 0.7976 79.76%
P-glycoprotein substrate - 0.5780 57.80%
CYP3A4 substrate + 0.6761 67.61%
CYP2C9 substrate - 0.5708 57.08%
CYP2D6 substrate - 0.7772 77.72%
CYP3A4 inhibition + 0.6322 63.22%
CYP2C9 inhibition - 0.6823 68.23%
CYP2C19 inhibition - 0.6144 61.44%
CYP2D6 inhibition - 0.9069 90.69%
CYP1A2 inhibition - 0.5637 56.37%
CYP2C8 inhibition - 0.7417 74.17%
CYP inhibitory promiscuity - 0.8222 82.22%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7643 76.43%
Carcinogenicity (trinary) Non-required 0.6480 64.80%
Eye corrosion - 0.9699 96.99%
Eye irritation - 0.8896 88.96%
Skin irritation - 0.6315 63.15%
Skin corrosion - 0.9070 90.70%
Ames mutagenesis - 0.6637 66.37%
Human Ether-a-go-go-Related Gene inhibition - 0.3604 36.04%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.6190 61.90%
skin sensitisation - 0.6681 66.81%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.4896 48.96%
Acute Oral Toxicity (c) III 0.6165 61.65%
Estrogen receptor binding + 0.7692 76.92%
Androgen receptor binding - 0.5373 53.73%
Thyroid receptor binding + 0.7064 70.64%
Glucocorticoid receptor binding + 0.7965 79.65%
Aromatase binding + 0.7730 77.30%
PPAR gamma - 0.5220 52.20%
Honey bee toxicity - 0.6040 60.40%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9482 94.82%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.02% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.01% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 93.64% 82.69%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.75% 91.11%
CHEMBL233 P35372 Mu opioid receptor 92.43% 97.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.45% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.41% 95.89%
CHEMBL218 P21554 Cannabinoid CB1 receptor 87.77% 96.61%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.08% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 85.76% 91.49%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 85.35% 95.50%
CHEMBL2996 Q05655 Protein kinase C delta 85.26% 97.79%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.94% 97.14%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 83.68% 98.33%
CHEMBL2534 O15530 3-phosphoinositide dependent protein kinase-1 82.71% 95.36%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.80% 85.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.70% 92.62%
CHEMBL2094135 Q96BI3 Gamma-secretase 81.60% 98.05%
CHEMBL2581 P07339 Cathepsin D 81.33% 98.95%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 81.13% 89.05%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.89% 86.33%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 80.19% 91.03%
CHEMBL238 Q01959 Dopamine transporter 80.00% 95.88%

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 163049415
LOTUS LTS0008392
wikiData Q105212147