7-Hydroxy-5-methoxyindan-1-spiro-cyclohexane

Details

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Internal ID 7a26f62f-20ae-44a6-95c6-7dc886ae16b6
Taxonomy Benzenoids > Indanes > Indan-1-spirocyclohexanes
IUPAC Name 6-methoxyspiro[1,2-dihydroindene-3,1'-cyclohexane]-4-ol
SMILES (Canonical) COC1=CC2=C(C(=C1)O)C3(CCCCC3)CC2
SMILES (Isomeric) COC1=CC2=C(C(=C1)O)C3(CCCCC3)CC2
InChI InChI=1S/C15H20O2/c1-17-12-9-11-5-8-15(6-3-2-4-7-15)14(11)13(16)10-12/h9-10,16H,2-8H2,1H3
InChI Key QMZSJEYAJUNUSB-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H20O2
Molecular Weight 232.32 g/mol
Exact Mass 232.146329876 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 4.70
Atomic LogP (AlogP) 3.55
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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7-hydroxy-5-methoxyindan-1-spiro-cyclohexane

2D Structure

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2D Structure of 7-Hydroxy-5-methoxyindan-1-spiro-cyclohexane

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 + 0.8818 88.18%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7650 76.50%
OATP2B1 inhibitior - 0.8515 85.15%
OATP1B1 inhibitior + 0.9050 90.50%
OATP1B3 inhibitior + 0.9721 97.21%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6055 60.55%
P-glycoprotein inhibitior - 0.9169 91.69%
P-glycoprotein substrate - 0.9140 91.40%
CYP3A4 substrate - 0.5254 52.54%
CYP2C9 substrate - 0.7786 77.86%
CYP2D6 substrate + 0.5128 51.28%
CYP3A4 inhibition - 0.8656 86.56%
CYP2C9 inhibition - 0.5919 59.19%
CYP2C19 inhibition + 0.6899 68.99%
CYP2D6 inhibition - 0.8723 87.23%
CYP1A2 inhibition + 0.8062 80.62%
CYP2C8 inhibition - 0.7485 74.85%
CYP inhibitory promiscuity - 0.6410 64.10%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6520 65.20%
Carcinogenicity (trinary) Non-required 0.3991 39.91%
Eye corrosion - 0.9517 95.17%
Eye irritation + 0.8812 88.12%
Skin irritation - 0.6089 60.89%
Skin corrosion - 0.9257 92.57%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3828 38.28%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.6320 63.20%
skin sensitisation - 0.8260 82.60%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6281 62.81%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.7260 72.60%
Acute Oral Toxicity (c) III 0.6862 68.62%
Estrogen receptor binding + 0.6065 60.65%
Androgen receptor binding + 0.6207 62.07%
Thyroid receptor binding + 0.5950 59.50%
Glucocorticoid receptor binding - 0.6593 65.93%
Aromatase binding - 0.5407 54.07%
PPAR gamma + 0.6512 65.12%
Honey bee toxicity - 0.9346 93.46%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.8747 87.47%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.94% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.18% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.77% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.39% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.24% 99.15%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 89.89% 93.40%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 88.50% 91.79%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.67% 93.99%
CHEMBL2581 P07339 Cathepsin D 85.37% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.05% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.84% 91.07%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 84.09% 92.68%
CHEMBL5203 P33316 dUTP pyrophosphatase 83.77% 99.18%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.76% 92.94%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.31% 94.00%
CHEMBL2535 P11166 Glucose transporter 81.01% 98.75%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 80.53% 100.00%
CHEMBL3085 P43003 Excitatory amino acid transporter 1 80.42% 94.67%
CHEMBL1929 P47989 Xanthine dehydrogenase 80.42% 96.12%

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.
Cannabis sativa

Cross-Links

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PubChem 117952889
LOTUS LTS0241016
wikiData Q105224278