(S)-3beta-Methyl-7,9-dimethoxy-3,4,5,10-tetrahydro-1H-naphtho[2,3-c]pyran-5,10-dione

Details

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Internal ID 7a8583e2-365e-42fe-a8e0-ca1efad1ce9c
Taxonomy Phenylpropanoids and polyketides > Isochromanequinones > Benzoisochromanequinones
IUPAC Name (3S)-7,9-dimethoxy-3-methyl-3,4-dihydro-1H-benzo[g]isochromene-5,10-dione
SMILES (Canonical) CC1CC2=C(CO1)C(=O)C3=C(C2=O)C=C(C=C3OC)OC
SMILES (Isomeric) C[C@H]1CC2=C(CO1)C(=O)C3=C(C2=O)C=C(C=C3OC)OC
InChI InChI=1S/C16H16O5/c1-8-4-10-12(7-21-8)16(18)14-11(15(10)17)5-9(19-2)6-13(14)20-3/h5-6,8H,4,7H2,1-3H3/t8-/m0/s1
InChI Key XOHGULAZSZLZHM-QMMMGPOBSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C16H16O5
Molecular Weight 288.29 g/mol
Exact Mass 288.09977361 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.19
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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(S)-3beta-Methyl-7,9-dimethoxy-3,4,5,10-tetrahydro-1H-naphtho[2,3-c]pyran-5,10-dione

2D Structure

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2D Structure of (S)-3beta-Methyl-7,9-dimethoxy-3,4,5,10-tetrahydro-1H-naphtho[2,3-c]pyran-5,10-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.8476 84.76%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7575 75.75%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9251 92.51%
OATP1B3 inhibitior + 0.9739 97.39%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5814 58.14%
P-glycoprotein inhibitior - 0.8144 81.44%
P-glycoprotein substrate - 0.8667 86.67%
CYP3A4 substrate + 0.5524 55.24%
CYP2C9 substrate - 0.5976 59.76%
CYP2D6 substrate - 0.7870 78.70%
CYP3A4 inhibition + 0.6510 65.10%
CYP2C9 inhibition - 0.6602 66.02%
CYP2C19 inhibition + 0.6727 67.27%
CYP2D6 inhibition - 0.8062 80.62%
CYP1A2 inhibition + 0.8747 87.47%
CYP2C8 inhibition - 0.8241 82.41%
CYP inhibitory promiscuity + 0.6022 60.22%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9213 92.13%
Carcinogenicity (trinary) Non-required 0.7240 72.40%
Eye corrosion - 0.9788 97.88%
Eye irritation + 0.7012 70.12%
Skin irritation - 0.7912 79.12%
Skin corrosion - 0.9701 97.01%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5782 57.82%
Micronuclear - 0.6100 61.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.7669 76.69%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.5092 50.92%
Estrogen receptor binding + 0.8179 81.79%
Androgen receptor binding + 0.6050 60.50%
Thyroid receptor binding - 0.5349 53.49%
Glucocorticoid receptor binding + 0.7610 76.10%
Aromatase binding - 0.4941 49.41%
PPAR gamma - 0.5073 50.73%
Honey bee toxicity - 0.7898 78.98%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9868 98.68%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.50% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.53% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.51% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.15% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.26% 86.33%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 87.41% 96.86%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.33% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.96% 89.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.93% 97.14%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 84.66% 96.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.62% 94.80%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.54% 92.94%
CHEMBL4208 P20618 Proteasome component C5 84.33% 90.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.03% 93.99%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.42% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.86% 90.71%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.58% 93.40%
CHEMBL2535 P11166 Glucose transporter 82.00% 98.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.63% 97.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.57% 96.00%
CHEMBL1907 P15144 Aminopeptidase N 81.52% 93.31%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 81.42% 92.38%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.59% 94.03%

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.
Morus mongolica
Senna alexandrina

Cross-Links

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PubChem 45257195
NPASS NPC277369
ChEMBL CHEMBL609285