4,7a-dimethyl-3-(2-methylprop-1-enyl)-2,3,3a,5,6,7-hexahydro-1H-indene-4,7-diol

Details

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Internal ID 9a2250ce-7760-482e-98f9-4fcbd8e5033a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 4,7a-dimethyl-3-(2-methylprop-1-enyl)-2,3,3a,5,6,7-hexahydro-1H-indene-4,7-diol
SMILES (Canonical) CC(=CC1CCC2(C1C(CCC2O)(C)O)C)C
SMILES (Isomeric) CC(=CC1CCC2(C1C(CCC2O)(C)O)C)C
InChI InChI=1S/C15H26O2/c1-10(2)9-11-5-7-14(3)12(16)6-8-15(4,17)13(11)14/h9,11-13,16-17H,5-8H2,1-4H3
InChI Key FKMCEEHVCIIPLE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O2
Molecular Weight 238.37 g/mol
Exact Mass 238.193280068 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.89
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,7a-dimethyl-3-(2-methylprop-1-enyl)-2,3,3a,5,6,7-hexahydro-1H-indene-4,7-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.5925 59.25%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5147 51.47%
OATP2B1 inhibitior - 0.8490 84.90%
OATP1B1 inhibitior + 0.9522 95.22%
OATP1B3 inhibitior + 0.9394 93.94%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7906 79.06%
P-glycoprotein inhibitior - 0.9559 95.59%
P-glycoprotein substrate - 0.8948 89.48%
CYP3A4 substrate + 0.5903 59.03%
CYP2C9 substrate - 0.5811 58.11%
CYP2D6 substrate - 0.7340 73.40%
CYP3A4 inhibition - 0.8340 83.40%
CYP2C9 inhibition - 0.9018 90.18%
CYP2C19 inhibition - 0.8621 86.21%
CYP2D6 inhibition - 0.9495 94.95%
CYP1A2 inhibition - 0.7339 73.39%
CYP2C8 inhibition - 0.9369 93.69%
CYP inhibitory promiscuity - 0.7426 74.26%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.5476 54.76%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.8215 82.15%
Skin irritation + 0.6893 68.93%
Skin corrosion - 0.9618 96.18%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6571 65.71%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5666 56.66%
skin sensitisation + 0.6538 65.38%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.6646 66.46%
Acute Oral Toxicity (c) III 0.7112 71.12%
Estrogen receptor binding - 0.6440 64.40%
Androgen receptor binding - 0.5803 58.03%
Thyroid receptor binding + 0.5230 52.30%
Glucocorticoid receptor binding - 0.6713 67.13%
Aromatase binding - 0.7073 70.73%
PPAR gamma - 0.7765 77.65%
Honey bee toxicity - 0.7832 78.32%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9692 96.92%

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 89.03% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.84% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.75% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 85.19% 94.75%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 85.08% 89.05%
CHEMBL226 P30542 Adenosine A1 receptor 83.35% 95.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.12% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.73% 82.69%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.68% 95.50%
CHEMBL1871 P10275 Androgen Receptor 81.46% 96.43%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 81.18% 95.58%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.22% 95.89%

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.
Chimonanthus praecox
Homalomena aromatica

Cross-Links

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PubChem 85401441
LOTUS LTS0264180
wikiData Q104996688