(1,1,7,7,7a-Pentamethyl-2,4,5,6-tetrahydroinden-2-yl)methanol

Details

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Internal ID e50e1884-d827-4b5e-bbae-41e2e291fefe
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name (1,1,7,7,7a-pentamethyl-2,4,5,6-tetrahydroinden-2-yl)methanol
SMILES (Canonical) CC1(CCCC2=CC(C(C21C)(C)C)CO)C
SMILES (Isomeric) CC1(CCCC2=CC(C(C21C)(C)C)CO)C
InChI InChI=1S/C15H26O/c1-13(2)8-6-7-11-9-12(10-16)14(3,4)15(11,13)5/h9,12,16H,6-8,10H2,1-5H3
InChI Key HPLQGFVYWQGCAW-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 3.90
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 (1,1,7,7,7a-Pentamethyl-2,4,5,6-tetrahydroinden-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 + 0.9949 99.49%
Caco-2 + 0.9504 95.04%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.8229 82.29%
OATP2B1 inhibitior - 0.8509 85.09%
OATP1B1 inhibitior + 0.8606 86.06%
OATP1B3 inhibitior - 0.2640 26.40%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8290 82.90%
P-glycoprotein inhibitior - 0.9519 95.19%
P-glycoprotein substrate - 0.8900 89.00%
CYP3A4 substrate - 0.5488 54.88%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate - 0.7388 73.88%
CYP3A4 inhibition - 0.8988 89.88%
CYP2C9 inhibition - 0.8456 84.56%
CYP2C19 inhibition - 0.8399 83.99%
CYP2D6 inhibition - 0.9143 91.43%
CYP1A2 inhibition - 0.8361 83.61%
CYP2C8 inhibition - 0.9278 92.78%
CYP inhibitory promiscuity - 0.6562 65.62%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6041 60.41%
Eye corrosion - 0.9580 95.80%
Eye irritation + 0.7974 79.74%
Skin irritation - 0.5190 51.90%
Skin corrosion - 0.9416 94.16%
Ames mutagenesis - 0.7264 72.64%
Human Ether-a-go-go-Related Gene inhibition - 0.6353 63.53%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6226 62.26%
skin sensitisation + 0.7152 71.52%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.7646 76.46%
Acute Oral Toxicity (c) III 0.7686 76.86%
Estrogen receptor binding - 0.7825 78.25%
Androgen receptor binding - 0.4899 48.99%
Thyroid receptor binding - 0.7156 71.56%
Glucocorticoid receptor binding - 0.7835 78.35%
Aromatase binding - 0.5841 58.41%
PPAR gamma - 0.8349 83.49%
Honey bee toxicity - 0.9230 92.30%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9727 97.27%

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 96.99% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.97% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.11% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 87.59% 94.75%
CHEMBL2581 P07339 Cathepsin D 84.63% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.37% 100.00%
CHEMBL226 P30542 Adenosine A1 receptor 84.29% 95.93%
CHEMBL2996 Q05655 Protein kinase C delta 83.69% 97.79%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.65% 97.09%

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 162922409
LOTUS LTS0107223
wikiData Q105031752