Neotenone

Details

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Internal ID d989516d-d2ee-48e0-937c-5feb42353bad
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > O-methylated isoflavonoids > 2-O-methylated isoflavonoids
IUPAC Name 6-(6-methoxy-1,3-benzodioxol-5-yl)-6,7-dihydrofuro[3,2-g]chromen-5-one
SMILES (Canonical) COC1=CC2=C(C=C1C3COC4=C(C3=O)C=C5C=COC5=C4)OCO2
SMILES (Isomeric) COC1=CC2=C(C=C1C3COC4=C(C3=O)C=C5C=COC5=C4)OCO2
InChI InChI=1S/C19H14O6/c1-21-15-7-18-17(24-9-25-18)5-11(15)13-8-23-16-6-14-10(2-3-22-14)4-12(16)19(13)20/h2-7,13H,8-9H2,1H3
InChI Key JZNIBAUSQWDFGE-UHFFFAOYSA-N
Popularity 19 references in papers

Physical and Chemical Properties

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Molecular Formula C19H14O6
Molecular Weight 338.30 g/mol
Exact Mass 338.07903816 g/mol
Topological Polar Surface Area (TPSA) 67.10 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.53
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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10091-02-8
Neorautenone
D08G5O2Y2W
6-(6-methoxy-1,3-benzodioxol-5-yl)-6,7-dihydrofuro[3,2-g]chromen-5-one
NSC361413
NSC-361413
5H-Furo(3,2-g)(1)benzopyran-5-one, 6,7-dihydro-6-(6-methoxy-1,3-benzodioxol-5-yl)-
6,7-Dihydro-6-(6-methoxy-1,3-benzodioxol-5-yl)-5H-furo(3,2-g)(1)benzopyran-5-one
6,7-Dihydro-6-(6-methoxy-1,3-benzodioxol-5-yl)-5H-furo[3,2-g][1]benzopyran-5-one
NSC 361413
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Neotenone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9883 98.83%
Caco-2 + 0.8511 85.11%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7443 74.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9430 94.30%
OATP1B3 inhibitior + 0.9884 98.84%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.8512 85.12%
P-glycoprotein inhibitior + 0.7462 74.62%
P-glycoprotein substrate - 0.7934 79.34%
CYP3A4 substrate + 0.5535 55.35%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7950 79.50%
CYP3A4 inhibition + 0.9146 91.46%
CYP2C9 inhibition + 0.9184 91.84%
CYP2C19 inhibition + 0.9748 97.48%
CYP2D6 inhibition + 0.7007 70.07%
CYP1A2 inhibition + 0.6115 61.15%
CYP2C8 inhibition - 0.6308 63.08%
CYP inhibitory promiscuity + 0.9431 94.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Warning 0.4065 40.65%
Eye corrosion - 0.9732 97.32%
Eye irritation - 0.7344 73.44%
Skin irritation - 0.7489 74.89%
Skin corrosion - 0.9568 95.68%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6624 66.24%
Micronuclear + 0.8274 82.74%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.7198 71.98%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.4917 49.17%
Acute Oral Toxicity (c) III 0.7513 75.13%
Estrogen receptor binding + 0.9286 92.86%
Androgen receptor binding + 0.7717 77.17%
Thyroid receptor binding - 0.5749 57.49%
Glucocorticoid receptor binding + 0.8288 82.88%
Aromatase binding - 0.5270 52.70%
PPAR gamma + 0.6670 66.70%
Honey bee toxicity - 0.7753 77.53%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9244 92.44%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 98.27% 96.77%
CHEMBL2581 P07339 Cathepsin D 95.91% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.73% 91.11%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 92.77% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.68% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.17% 95.56%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 88.58% 82.67%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.10% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.74% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.62% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.26% 96.09%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.16% 89.62%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.92% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.76% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.70% 97.14%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 85.26% 80.96%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.08% 94.80%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.17% 97.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.01% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.08% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.97% 94.45%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.24% 94.03%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.00% 93.99%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.90% 85.14%

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.
Neorautanenia mitis
Pachyrhizus erosus
Pachyrhizus tuberosus

Cross-Links

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PubChem 73603
LOTUS LTS0190370
wikiData Q104401722