8-(2-hydroxypropan-2-yl)-2,5-dimethyl-2,3,4,4a,6,7,8,8a-octahydro-1H-naphthalene-1,5-diol

Details

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Internal ID 4af4ef20-3351-4a18-8a08-98d37c35f720
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 8-(2-hydroxypropan-2-yl)-2,5-dimethyl-2,3,4,4a,6,7,8,8a-octahydro-1H-naphthalene-1,5-diol
SMILES (Canonical) CC1CCC2C(C1O)C(CCC2(C)O)C(C)(C)O
SMILES (Isomeric) CC1CCC2C(C1O)C(CCC2(C)O)C(C)(C)O
InChI InChI=1S/C15H28O3/c1-9-5-6-11-12(13(9)16)10(14(2,3)17)7-8-15(11,4)18/h9-13,16-18H,5-8H2,1-4H3
InChI Key GCABARKLIDPDND-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 1.70
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 8-(2-hydroxypropan-2-yl)-2,5-dimethyl-2,3,4,4a,6,7,8,8a-octahydro-1H-naphthalene-1,5-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.5729 57.29%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6957 69.57%
OATP2B1 inhibitior - 0.8471 84.71%
OATP1B1 inhibitior + 0.9293 92.93%
OATP1B3 inhibitior + 0.9756 97.56%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9238 92.38%
P-glycoprotein inhibitior - 0.9150 91.50%
P-glycoprotein substrate - 0.8456 84.56%
CYP3A4 substrate + 0.6134 61.34%
CYP2C9 substrate - 0.5955 59.55%
CYP2D6 substrate - 0.6719 67.19%
CYP3A4 inhibition - 0.8623 86.23%
CYP2C9 inhibition - 0.8910 89.10%
CYP2C19 inhibition - 0.9175 91.75%
CYP2D6 inhibition - 0.9718 97.18%
CYP1A2 inhibition - 0.7633 76.33%
CYP2C8 inhibition - 0.6934 69.34%
CYP inhibitory promiscuity - 0.9359 93.59%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6844 68.44%
Eye corrosion - 0.9826 98.26%
Eye irritation - 0.7537 75.37%
Skin irritation + 0.5424 54.24%
Skin corrosion - 0.9404 94.04%
Ames mutagenesis - 0.7653 76.53%
Human Ether-a-go-go-Related Gene inhibition - 0.6270 62.70%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5427 54.27%
skin sensitisation + 0.4937 49.37%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.7558 75.58%
Acute Oral Toxicity (c) III 0.7991 79.91%
Estrogen receptor binding - 0.6873 68.73%
Androgen receptor binding - 0.5825 58.25%
Thyroid receptor binding + 0.5330 53.30%
Glucocorticoid receptor binding - 0.5959 59.59%
Aromatase binding - 0.7334 73.34%
PPAR gamma - 0.8039 80.39%
Honey bee toxicity - 0.8342 83.42%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9630 96.30%

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 98.21% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.50% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.13% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 88.88% 83.82%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.46% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.94% 93.04%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.69% 97.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.82% 97.14%
CHEMBL1871 P10275 Androgen Receptor 82.27% 96.43%
CHEMBL2581 P07339 Cathepsin D 82.17% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.16% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.72% 92.94%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.07% 96.77%
CHEMBL226 P30542 Adenosine A1 receptor 80.94% 95.93%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 80.62% 100.00%

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.
Dorstenia psilurus
Ferula communis

Cross-Links

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PubChem 85196090
LOTUS LTS0232322
wikiData Q105207333