2-Methyl-2,5,6-bornantriol

Details

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Internal ID 51d55202-8446-45be-9ac5-fb1953582fb1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name (1R,2S,3R,4S,5R)-4,5,7,7-tetramethylbicyclo[2.2.1]heptane-2,3,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H20O3/c1-9(2)6-5-10(3,14)11(9,4)8(13)7(6)12/h6-8,12-14H,5H2,1-4H3/t6-,7-,8-,10+,11+/m0/s1
InChI Key GRLGJKOBRSOQMC-MZFCOBPBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H20O3
Molecular Weight 200.27 g/mol
Exact Mass 200.14124450 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.53
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Methyl-2,5,6-bornantriol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9521 95.21%
Caco-2 - 0.6709 67.09%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.4730 47.30%
OATP2B1 inhibitior - 0.8536 85.36%
OATP1B1 inhibitior + 0.9727 97.27%
OATP1B3 inhibitior + 0.9614 96.14%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9361 93.61%
P-glycoprotein inhibitior - 0.9737 97.37%
P-glycoprotein substrate - 0.9154 91.54%
CYP3A4 substrate - 0.5609 56.09%
CYP2C9 substrate - 0.5853 58.53%
CYP2D6 substrate - 0.7825 78.25%
CYP3A4 inhibition - 0.8785 87.85%
CYP2C9 inhibition - 0.8592 85.92%
CYP2C19 inhibition - 0.8526 85.26%
CYP2D6 inhibition - 0.9493 94.93%
CYP1A2 inhibition - 0.8224 82.24%
CYP2C8 inhibition - 0.9547 95.47%
CYP inhibitory promiscuity - 0.9535 95.35%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5612 56.12%
Eye corrosion - 0.9778 97.78%
Eye irritation - 0.7108 71.08%
Skin irritation + 0.5230 52.30%
Skin corrosion - 0.7783 77.83%
Ames mutagenesis - 0.7128 71.28%
Human Ether-a-go-go-Related Gene inhibition - 0.6841 68.41%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.5684 56.84%
skin sensitisation - 0.5457 54.57%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.6230 62.30%
Acute Oral Toxicity (c) III 0.6395 63.95%
Estrogen receptor binding - 0.7285 72.85%
Androgen receptor binding - 0.5712 57.12%
Thyroid receptor binding - 0.6945 69.45%
Glucocorticoid receptor binding - 0.8360 83.60%
Aromatase binding - 0.7475 74.75%
PPAR gamma - 0.7054 70.54%
Honey bee toxicity - 0.9116 91.16%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.7136 71.36%

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 95.66% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 90.46% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.63% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.71% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.59% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.07% 97.25%

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 56954716
LOTUS LTS0252811
wikiData Q77372834