(3,3,4,5,7a-pentamethyl-2,3a,6,7-tetrahydro-1H-inden-2-yl)methanol

Details

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Internal ID a9cf7e35-56ed-4274-8baa-c1f8309599eb
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name (3,3,4,5,7a-pentamethyl-2,3a,6,7-tetrahydro-1H-inden-2-yl)methanol
SMILES (Canonical) CC1=C(C2C(C(CC2(CC1)C)CO)(C)C)C
SMILES (Isomeric) CC1=C(C2C(C(CC2(CC1)C)CO)(C)C)C
InChI InChI=1S/C15H26O/c1-10-6-7-15(5)8-12(9-16)14(3,4)13(15)11(10)2/h12-13,16H,6-9H2,1-5H3
InChI Key LFLBXCLVRYZDOG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.78
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3,3,4,5,7a-pentamethyl-2,3a,6,7-tetrahydro-1H-inden-2-yl)methanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.8477 84.77%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.7768 77.68%
OATP2B1 inhibitior - 0.8440 84.40%
OATP1B1 inhibitior + 0.9039 90.39%
OATP1B3 inhibitior - 0.2281 22.81%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9021 90.21%
P-glycoprotein inhibitior - 0.9349 93.49%
P-glycoprotein substrate - 0.8850 88.50%
CYP3A4 substrate - 0.5170 51.70%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate - 0.7388 73.88%
CYP3A4 inhibition - 0.7774 77.74%
CYP2C9 inhibition - 0.7771 77.71%
CYP2C19 inhibition - 0.8542 85.42%
CYP2D6 inhibition - 0.9245 92.45%
CYP1A2 inhibition - 0.8602 86.02%
CYP2C8 inhibition - 0.8968 89.68%
CYP inhibitory promiscuity - 0.6410 64.10%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6066 60.66%
Eye corrosion - 0.9615 96.15%
Eye irritation + 0.7175 71.75%
Skin irritation - 0.6668 66.68%
Skin corrosion - 0.9701 97.01%
Ames mutagenesis - 0.6237 62.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5569 55.69%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5839 58.39%
skin sensitisation + 0.7309 73.09%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6798 67.98%
Acute Oral Toxicity (c) III 0.6723 67.23%
Estrogen receptor binding - 0.7462 74.62%
Androgen receptor binding - 0.5765 57.65%
Thyroid receptor binding - 0.6141 61.41%
Glucocorticoid receptor binding - 0.6804 68.04%
Aromatase binding - 0.5958 59.58%
PPAR gamma - 0.7316 73.16%
Honey bee toxicity - 0.9186 91.86%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9910 99.10%

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 95.51% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.76% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.77% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.66% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.58% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.94% 95.89%
CHEMBL2581 P07339 Cathepsin D 80.44% 98.95%
CHEMBL2996 Q05655 Protein kinase C delta 80.22% 97.79%

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.
Ligusticum grayi

Cross-Links

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PubChem 163030582
LOTUS LTS0195294
wikiData Q105151060