Hypoxylan A

Details

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Internal ID 9763f37e-5f8d-45f5-b21d-6dee077b36da
Taxonomy Benzenoids > Tetralins
IUPAC Name (5S)-3-(1-hydroxypropan-2-yl)-5-methyl-5,6,7,8-tetrahydronaphthalen-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H20O2/c1-9-4-3-5-11-6-14(16)13(7-12(9)11)10(2)8-15/h6-7,9-10,15-16H,3-5,8H2,1-2H3/t9-,10?/m0/s1
InChI Key DKBQCOYMWZZNQT-RGURZIINSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H20O2
Molecular Weight 220.31 g/mol
Exact Mass 220.146329876 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.93
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Hypoxylan A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.8423 84.23%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7377 73.77%
OATP2B1 inhibitior - 0.8530 85.30%
OATP1B1 inhibitior + 0.8937 89.37%
OATP1B3 inhibitior + 0.8378 83.78%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8242 82.42%
P-glycoprotein inhibitior - 0.9404 94.04%
P-glycoprotein substrate - 0.7950 79.50%
CYP3A4 substrate - 0.5537 55.37%
CYP2C9 substrate + 0.5914 59.14%
CYP2D6 substrate + 0.4078 40.78%
CYP3A4 inhibition - 0.7643 76.43%
CYP2C9 inhibition - 0.6455 64.55%
CYP2C19 inhibition - 0.5416 54.16%
CYP2D6 inhibition - 0.8599 85.99%
CYP1A2 inhibition + 0.9568 95.68%
CYP2C8 inhibition - 0.9248 92.48%
CYP inhibitory promiscuity + 0.5955 59.55%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.6765 67.65%
Eye corrosion - 0.9491 94.91%
Eye irritation - 0.5959 59.59%
Skin irritation - 0.6835 68.35%
Skin corrosion - 0.7917 79.17%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4816 48.16%
Micronuclear - 0.9241 92.41%
Hepatotoxicity - 0.5915 59.15%
skin sensitisation + 0.5126 51.26%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.8852 88.52%
Acute Oral Toxicity (c) III 0.5674 56.74%
Estrogen receptor binding - 0.7803 78.03%
Androgen receptor binding - 0.7794 77.94%
Thyroid receptor binding + 0.5892 58.92%
Glucocorticoid receptor binding - 0.6909 69.09%
Aromatase binding - 0.8181 81.81%
PPAR gamma - 0.7175 71.75%
Honey bee toxicity - 0.9527 95.27%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9758 97.58%

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 97.58% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.25% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.85% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.79% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.38% 97.25%
CHEMBL5203 P33316 dUTP pyrophosphatase 85.91% 99.18%
CHEMBL4581 P52732 Kinesin-like protein 1 85.35% 93.18%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.28% 90.71%
CHEMBL1951 P21397 Monoamine oxidase A 85.05% 91.49%
CHEMBL226 P30542 Adenosine A1 receptor 84.41% 95.93%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.24% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.16% 100.00%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 83.68% 97.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.25% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.81% 95.56%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.75% 90.24%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.54% 93.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.43% 93.99%
CHEMBL213 P08588 Beta-1 adrenergic receptor 80.92% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.16% 92.62%

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 122390637
LOTUS LTS0098692
wikiData Q104982981