Hypoxylonol B

Details

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Internal ID 14d203fe-aa42-4b72-aa39-b8a0870273a7
Taxonomy Lignans, neolignans and related compounds
IUPAC Name 7,15,19-trihydroxy-18-methoxypentacyclo[10.7.1.02,11.03,8.016,20]icosa-1,3(8),4,6,12(20),13,15-heptaen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H18O5/c1-26-16-8-12-13(22)6-5-9-11-7-15(24)19-10(3-2-4-14(19)23)18(11)20(17(9)12)21(16)25/h2-6,11,16,21-23,25H,7-8H2,1H3
InChI Key KVGCXSKAIUCSKN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H18O5
Molecular Weight 350.40 g/mol
Exact Mass 350.11542367 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 1.70
Atomic LogP (AlogP) 2.62
H-Bond Acceptor 5
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 Hypoxylonol B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 + 0.6144 61.44%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7670 76.70%
OATP2B1 inhibitior - 0.5815 58.15%
OATP1B1 inhibitior + 0.9157 91.57%
OATP1B3 inhibitior + 0.9651 96.51%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6599 65.99%
P-glycoprotein inhibitior - 0.6578 65.78%
P-glycoprotein substrate - 0.6872 68.72%
CYP3A4 substrate + 0.6456 64.56%
CYP2C9 substrate - 0.7940 79.40%
CYP2D6 substrate - 0.8005 80.05%
CYP3A4 inhibition - 0.7660 76.60%
CYP2C9 inhibition + 0.7421 74.21%
CYP2C19 inhibition + 0.7741 77.41%
CYP2D6 inhibition - 0.6263 62.63%
CYP1A2 inhibition + 0.9455 94.55%
CYP2C8 inhibition + 0.4835 48.35%
CYP inhibitory promiscuity + 0.7523 75.23%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9520 95.20%
Carcinogenicity (trinary) Non-required 0.5218 52.18%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.7926 79.26%
Skin irritation - 0.6246 62.46%
Skin corrosion - 0.9409 94.09%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6041 60.41%
Micronuclear + 0.5859 58.59%
Hepatotoxicity + 0.5907 59.07%
skin sensitisation - 0.7760 77.60%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.8318 83.18%
Acute Oral Toxicity (c) III 0.3920 39.20%
Estrogen receptor binding + 0.8194 81.94%
Androgen receptor binding + 0.6986 69.86%
Thyroid receptor binding - 0.5853 58.53%
Glucocorticoid receptor binding + 0.8531 85.31%
Aromatase binding - 0.6030 60.30%
PPAR gamma + 0.8219 82.19%
Honey bee toxicity - 0.8244 82.44%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9909 99.09%

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
CHEMBL2581 P07339 Cathepsin D 98.53% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.56% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.45% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.27% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.72% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.63% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 90.19% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.82% 99.23%
CHEMBL2535 P11166 Glucose transporter 88.72% 98.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.72% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.13% 95.89%
CHEMBL2056 P21728 Dopamine D1 receptor 85.73% 91.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.85% 99.15%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 84.60% 92.88%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.76% 93.03%
CHEMBL1902 P62942 FK506-binding protein 1A 82.72% 97.05%
CHEMBL1907 P15144 Aminopeptidase N 81.52% 93.31%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.06% 99.17%

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 139583858
LOTUS LTS0181002
wikiData Q75068427