(1R,2S,5S,6S,9R,11S)-5-isothiocyanato-5,9-dimethyl-2-propan-2-yl-10,12-dioxatricyclo[7.2.1.01,6]dodecan-11-ol

Details

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Internal ID 3cb431fe-fc4f-465a-b48e-086d5037e678
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (1R,2S,5S,6S,9R,11S)-5-isothiocyanato-5,9-dimethyl-2-propan-2-yl-10,12-dioxatricyclo[7.2.1.01,6]dodecan-11-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H25NO3S/c1-10(2)11-5-7-14(3,17-9-21)12-6-8-15(4)19-13(18)16(11,12)20-15/h10-13,18H,5-8H2,1-4H3/t11-,12-,13-,14-,15-,16+/m0/s1
InChI Key LJLZJJKLXWEJAB-OJFNHCPVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H25NO3S
Molecular Weight 311.40 g/mol
Exact Mass 311.15551483 g/mol
Topological Polar Surface Area (TPSA) 83.10 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.14
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,2S,5S,6S,9R,11S)-5-isothiocyanato-5,9-dimethyl-2-propan-2-yl-10,12-dioxatricyclo[7.2.1.01,6]dodecan-11-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8947 89.47%
Caco-2 + 0.6896 68.96%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.4683 46.83%
OATP2B1 inhibitior - 0.8508 85.08%
OATP1B1 inhibitior + 0.9148 91.48%
OATP1B3 inhibitior + 0.9231 92.31%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.8972 89.72%
P-glycoprotein inhibitior - 0.8220 82.20%
P-glycoprotein substrate - 0.8461 84.61%
CYP3A4 substrate + 0.5952 59.52%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7645 76.45%
CYP3A4 inhibition - 0.9652 96.52%
CYP2C9 inhibition - 0.7919 79.19%
CYP2C19 inhibition - 0.7031 70.31%
CYP2D6 inhibition - 0.9049 90.49%
CYP1A2 inhibition - 0.7616 76.16%
CYP2C8 inhibition - 0.8095 80.95%
CYP inhibitory promiscuity - 0.8585 85.85%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.5971 59.71%
Eye corrosion - 0.9801 98.01%
Eye irritation - 0.9108 91.08%
Skin irritation - 0.7478 74.78%
Skin corrosion - 0.8902 89.02%
Ames mutagenesis - 0.5414 54.14%
Human Ether-a-go-go-Related Gene inhibition - 0.6280 62.80%
Micronuclear - 0.6400 64.00%
Hepatotoxicity - 0.5683 56.83%
skin sensitisation - 0.7649 76.49%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.4894 48.94%
Acute Oral Toxicity (c) III 0.5913 59.13%
Estrogen receptor binding + 0.6630 66.30%
Androgen receptor binding + 0.6703 67.03%
Thyroid receptor binding + 0.6757 67.57%
Glucocorticoid receptor binding - 0.6850 68.50%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.6201 62.01%
Honey bee toxicity - 0.7211 72.11%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.8419 84.19%

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
CHEMBL218 P21554 Cannabinoid CB1 receptor 96.48% 96.61%
CHEMBL226 P30542 Adenosine A1 receptor 96.04% 95.93%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.00% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.36% 96.09%
CHEMBL2179 P04062 Beta-glucocerebrosidase 92.70% 85.31%
CHEMBL3837 P07711 Cathepsin L 91.83% 96.61%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 91.58% 95.58%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.98% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.95% 95.89%
CHEMBL284 P27487 Dipeptidyl peptidase IV 88.59% 95.69%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 87.04% 96.38%
CHEMBL1871 P10275 Androgen Receptor 86.18% 96.43%
CHEMBL2996 Q05655 Protein kinase C delta 85.76% 97.79%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 85.41% 95.34%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.86% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.36% 97.14%
CHEMBL4072 P07858 Cathepsin B 83.99% 93.67%
CHEMBL221 P23219 Cyclooxygenase-1 83.82% 90.17%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 83.78% 91.03%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 83.43% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.12% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.81% 89.00%
CHEMBL259 P32245 Melanocortin receptor 4 82.79% 95.38%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 82.56% 95.83%
CHEMBL299 P17252 Protein kinase C alpha 80.37% 98.03%

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 24858026
LOTUS LTS0151584
wikiData Q105152653