Eutypellol B

Details

Top
Internal ID f1fdab40-b3ae-4308-9f08-982f0f034f30
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name [(1S,6R,7S)-3,7-dimethyl-7-bicyclo[4.1.0]hept-2-enyl]methanol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O/c1-7-3-4-8-9(5-7)10(8,2)6-11/h5,8-9,11H,3-4,6H2,1-2H3/t8-,9+,10+/m1/s1
InChI Key XTKWHWITBUCBCZ-UTLUCORTSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.97
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Eutypellol B

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9843 98.43%
Caco-2 + 0.7891 78.91%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.8389 83.89%
OATP2B1 inhibitior - 0.8459 84.59%
OATP1B1 inhibitior + 0.9281 92.81%
OATP1B3 inhibitior + 0.9035 90.35%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9191 91.91%
P-glycoprotein inhibitior - 0.9707 97.07%
P-glycoprotein substrate - 0.9287 92.87%
CYP3A4 substrate - 0.5129 51.29%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate - 0.7388 73.88%
CYP3A4 inhibition - 0.8534 85.34%
CYP2C9 inhibition - 0.7439 74.39%
CYP2C19 inhibition - 0.7688 76.88%
CYP2D6 inhibition - 0.8798 87.98%
CYP1A2 inhibition - 0.7517 75.17%
CYP2C8 inhibition - 0.8669 86.69%
CYP inhibitory promiscuity - 0.7980 79.80%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6294 62.94%
Eye corrosion - 0.8861 88.61%
Eye irritation + 0.6092 60.92%
Skin irritation - 0.6081 60.81%
Skin corrosion - 0.9739 97.39%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6068 60.68%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.5062 50.62%
skin sensitisation + 0.7675 76.75%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.6259 62.59%
Acute Oral Toxicity (c) III 0.8306 83.06%
Estrogen receptor binding - 0.9223 92.23%
Androgen receptor binding - 0.6516 65.16%
Thyroid receptor binding - 0.8779 87.79%
Glucocorticoid receptor binding - 0.8658 86.58%
Aromatase binding - 0.8663 86.63%
PPAR gamma - 0.8709 87.09%
Honey bee toxicity - 0.9523 95.23%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9761 97.61%

Targets

Top

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 93.21% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.08% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.81% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.72% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.98% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 84.47% 97.79%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.46% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.91% 95.89%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 80.16% 89.05%

Plants that contains it

Top
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

Top
PubChem 139591314
LOTUS LTS0119441
wikiData Q105341632