12a-Hydroxymunduserone

Details

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Internal ID f1535a96-1474-4e58-abf6-b0dceab882ca
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Rotenoids > Rotenones
IUPAC Name 12a-hydroxy-2,3,9-trimethoxy-6,6a-dihydrochromeno[3,4-b]chromen-12-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H18O7/c1-22-10-4-5-11-13(6-10)26-17-9-25-14-8-16(24-3)15(23-2)7-12(14)19(17,21)18(11)20/h4-8,17,21H,9H2,1-3H3
InChI Key APAWOEBSLLGWDF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18O7
Molecular Weight 358.30 g/mol
Exact Mass 358.10525291 g/mol
Topological Polar Surface Area (TPSA) 83.50 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.94
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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12alpha-Hydroxymunduserone
CHEBI:175596
LMPK12060051
12a-hydroxy-2,3,9-trimethoxy-6,6a-dihydrochromeno[3,4-b]chromen-12-one

2D Structure

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2D Structure of 12a-Hydroxymunduserone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9758 97.58%
Caco-2 + 0.8200 82.00%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7713 77.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9403 94.03%
OATP1B3 inhibitior + 0.9649 96.49%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6230 62.30%
P-glycoprotein inhibitior + 0.7103 71.03%
P-glycoprotein substrate - 0.6576 65.76%
CYP3A4 substrate + 0.5985 59.85%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7088 70.88%
CYP3A4 inhibition - 0.5305 53.05%
CYP2C9 inhibition - 0.9386 93.86%
CYP2C19 inhibition - 0.5100 51.00%
CYP2D6 inhibition - 0.8414 84.14%
CYP1A2 inhibition + 0.6314 63.14%
CYP2C8 inhibition - 0.7546 75.46%
CYP inhibitory promiscuity - 0.8323 83.23%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6113 61.13%
Eye corrosion - 0.9861 98.61%
Eye irritation - 0.6837 68.37%
Skin irritation - 0.8080 80.80%
Skin corrosion - 0.9711 97.11%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7904 79.04%
Micronuclear + 0.6659 66.59%
Hepatotoxicity - 0.5801 58.01%
skin sensitisation - 0.8502 85.02%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.5918 59.18%
Acute Oral Toxicity (c) III 0.5955 59.55%
Estrogen receptor binding + 0.9061 90.61%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.7674 76.74%
Glucocorticoid receptor binding + 0.7412 74.12%
Aromatase binding - 0.5318 53.18%
PPAR gamma + 0.7814 78.14%
Honey bee toxicity - 0.8171 81.71%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5251 52.51%
Fish aquatic toxicity + 0.6947 69.47%

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 97.35% 91.11%
CHEMBL4208 P20618 Proteasome component C5 94.73% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.28% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.95% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.46% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.68% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.28% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.96% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.31% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.16% 92.62%
CHEMBL2581 P07339 Cathepsin D 85.03% 98.95%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.95% 96.77%
CHEMBL3492 P49721 Proteasome Macropain subunit 84.51% 90.24%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.24% 94.80%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.98% 97.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.59% 89.00%
CHEMBL1907 P15144 Aminopeptidase N 83.15% 93.31%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 82.62% 96.86%
CHEMBL2535 P11166 Glucose transporter 81.54% 98.75%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.35% 91.07%

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.
Tephrosia fulvinervis

Cross-Links

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PubChem 14427372
LOTUS LTS0242494
wikiData Q104916160