1,6,6-trimethyl-4-propan-2-yl-2,3,4,5-tetrahydro-1H-inden-3a-ol

Details

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Internal ID 65584edd-a2a9-4278-a7d0-adabf5ef45bd
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,6,6-trimethyl-4-propan-2-yl-2,3,4,5-tetrahydro-1H-inden-3a-ol
SMILES (Canonical) CC1CCC2(C1=CC(CC2C(C)C)(C)C)O
SMILES (Isomeric) CC1CCC2(C1=CC(CC2C(C)C)(C)C)O
InChI InChI=1S/C15H26O/c1-10(2)12-8-14(4,5)9-13-11(3)6-7-15(12,13)16/h9-12,16H,6-8H2,1-5H3
InChI Key XDLCURIUCCHLSA-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 3.50
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 1,6,6-trimethyl-4-propan-2-yl-2,3,4,5-tetrahydro-1H-inden-3a-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.7712 77.12%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.4720 47.20%
OATP2B1 inhibitior - 0.8388 83.88%
OATP1B1 inhibitior + 0.9425 94.25%
OATP1B3 inhibitior + 0.9578 95.78%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9151 91.51%
P-glycoprotein inhibitior - 0.9194 91.94%
P-glycoprotein substrate - 0.7878 78.78%
CYP3A4 substrate + 0.5358 53.58%
CYP2C9 substrate + 0.5024 50.24%
CYP2D6 substrate - 0.7533 75.33%
CYP3A4 inhibition - 0.9118 91.18%
CYP2C9 inhibition - 0.8273 82.73%
CYP2C19 inhibition - 0.7865 78.65%
CYP2D6 inhibition - 0.9464 94.64%
CYP1A2 inhibition - 0.8108 81.08%
CYP2C8 inhibition - 0.9653 96.53%
CYP inhibitory promiscuity - 0.7833 78.33%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5435 54.35%
Eye corrosion - 0.9819 98.19%
Eye irritation - 0.5000 50.00%
Skin irritation + 0.7878 78.78%
Skin corrosion - 0.9457 94.57%
Ames mutagenesis - 0.7270 72.70%
Human Ether-a-go-go-Related Gene inhibition - 0.3603 36.03%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5108 51.08%
skin sensitisation + 0.6451 64.51%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.8364 83.64%
Acute Oral Toxicity (c) III 0.7797 77.97%
Estrogen receptor binding - 0.9045 90.45%
Androgen receptor binding - 0.5290 52.90%
Thyroid receptor binding - 0.6511 65.11%
Glucocorticoid receptor binding - 0.7503 75.03%
Aromatase binding - 0.7178 71.78%
PPAR gamma - 0.8499 84.99%
Honey bee toxicity - 0.9422 94.22%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9767 97.67%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.73% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.16% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 94.32% 82.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.24% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.00% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.93% 100.00%
CHEMBL2581 P07339 Cathepsin D 83.59% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.04% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.38% 95.89%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.15% 93.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 75033505
LOTUS LTS0256429
wikiData Q105325802