4-(hydroxymethyl)-3,4a,8,8-tetramethyl-2,4,5,6,7,8a-hexahydro-1H-naphthalene-2,3-diol

Details

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Internal ID 89edbbd1-022b-4e3b-bc73-063b431232e9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 4-(hydroxymethyl)-3,4a,8,8-tetramethyl-2,4,5,6,7,8a-hexahydro-1H-naphthalene-2,3-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H28O3/c1-13(2)6-5-7-14(3)10(13)8-12(17)15(4,18)11(14)9-16/h10-12,16-18H,5-9H2,1-4H3
InChI Key BLJQFAPBVZSBOZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H28O3
Molecular Weight 256.38 g/mol
Exact Mass 256.20384475 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 2.90
Atomic LogP (AlogP) 1.94
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(hydroxymethyl)-3,4a,8,8-tetramethyl-2,4,5,6,7,8a-hexahydro-1H-naphthalene-2,3-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9670 96.70%
Caco-2 + 0.6015 60.15%
Blood Brain Barrier + 0.7135 71.35%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6413 64.13%
OATP2B1 inhibitior - 0.8477 84.77%
OATP1B1 inhibitior + 0.9047 90.47%
OATP1B3 inhibitior + 0.8948 89.48%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7650 76.50%
BSEP inhibitior - 0.8098 80.98%
P-glycoprotein inhibitior - 0.9481 94.81%
P-glycoprotein substrate - 0.9140 91.40%
CYP3A4 substrate + 0.5506 55.06%
CYP2C9 substrate - 0.5963 59.63%
CYP2D6 substrate - 0.7575 75.75%
CYP3A4 inhibition - 0.8857 88.57%
CYP2C9 inhibition - 0.7483 74.83%
CYP2C19 inhibition - 0.8310 83.10%
CYP2D6 inhibition - 0.9600 96.00%
CYP1A2 inhibition - 0.7330 73.30%
CYP2C8 inhibition - 0.8655 86.55%
CYP inhibitory promiscuity - 0.9520 95.20%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.7255 72.55%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.4883 48.83%
Skin irritation - 0.6483 64.83%
Skin corrosion - 0.9598 95.98%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5908 59.08%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.6249 62.49%
skin sensitisation - 0.7837 78.37%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7518 75.18%
Acute Oral Toxicity (c) III 0.7182 71.82%
Estrogen receptor binding - 0.5843 58.43%
Androgen receptor binding - 0.6434 64.34%
Thyroid receptor binding - 0.5756 57.56%
Glucocorticoid receptor binding - 0.5427 54.27%
Aromatase binding - 0.6996 69.96%
PPAR gamma - 0.7386 73.86%
Honey bee toxicity - 0.9008 90.08%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.8769 87.69%

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 97.51% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.73% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.82% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.72% 96.09%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 86.52% 95.50%
CHEMBL2996 Q05655 Protein kinase C delta 86.13% 97.79%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.69% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.41% 96.95%
CHEMBL218 P21554 Cannabinoid CB1 receptor 83.95% 96.61%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.32% 82.69%
CHEMBL4370 P16662 UDP-glucuronosyltransferase 2B7 82.18% 100.00%
CHEMBL206 P03372 Estrogen receptor alpha 81.04% 97.64%

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 85373956
LOTUS LTS0001615
wikiData Q104938052