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

Details

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Internal ID d9163680-2d29-4d82-a3d5-01347838144b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name (3,3,4,5,7a-pentamethyl-2,5,6,7-tetrahydro-1H-inden-2-yl)methanol
SMILES (Canonical) CC1CCC2(CC(C(C2=C1C)(C)C)CO)C
SMILES (Isomeric) CC1CCC2(CC(C(C2=C1C)(C)C)CO)C
InChI InChI=1S/C15H26O/c1-10-6-7-15(5)8-12(9-16)14(3,4)13(15)11(10)2/h10,12,16H,6-9H2,1-5H3
InChI Key CUFZOTYNOCYVBK-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 3.40
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-2,5,6,7-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 + 0.9961 99.61%
Caco-2 + 0.8253 82.53%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.7391 73.91%
OATP2B1 inhibitior - 0.8479 84.79%
OATP1B1 inhibitior + 0.9064 90.64%
OATP1B3 inhibitior + 0.8104 81.04%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9082 90.82%
P-glycoprotein inhibitior - 0.9270 92.70%
P-glycoprotein substrate - 0.8545 85.45%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate - 0.7388 73.88%
CYP3A4 inhibition - 0.8317 83.17%
CYP2C9 inhibition - 0.7437 74.37%
CYP2C19 inhibition - 0.8306 83.06%
CYP2D6 inhibition - 0.9223 92.23%
CYP1A2 inhibition - 0.8527 85.27%
CYP2C8 inhibition - 0.8749 87.49%
CYP inhibitory promiscuity - 0.6414 64.14%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5986 59.86%
Eye corrosion - 0.9637 96.37%
Eye irritation + 0.7578 75.78%
Skin irritation - 0.6854 68.54%
Skin corrosion - 0.9673 96.73%
Ames mutagenesis - 0.6237 62.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5334 53.34%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5142 51.42%
skin sensitisation + 0.6797 67.97%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.6626 66.26%
Acute Oral Toxicity (c) III 0.5961 59.61%
Estrogen receptor binding - 0.8122 81.22%
Androgen receptor binding - 0.7111 71.11%
Thyroid receptor binding - 0.5608 56.08%
Glucocorticoid receptor binding - 0.7528 75.28%
Aromatase binding - 0.5671 56.71%
PPAR gamma - 0.8088 80.88%
Honey bee toxicity - 0.9335 93.35%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9919 99.19%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.70% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.73% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.10% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.08% 91.11%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 85.00% 95.50%
CHEMBL218 P21554 Cannabinoid CB1 receptor 82.90% 96.61%

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 163096693
LOTUS LTS0166415
wikiData Q104970227