7-Desmethylherbarin

Details

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Internal ID 7d55007c-6c89-4e57-9909-403aa256112f
Taxonomy Phenylpropanoids and polyketides > Isochromanequinones > Benzoisochromanequinones
IUPAC Name 3,7-dihydroxy-9-methoxy-3-methyl-1,4-dihydrobenzo[g]isochromene-5,10-dione
SMILES (Canonical) CC1(CC2=C(CO1)C(=O)C3=C(C2=O)C=C(C=C3OC)O)O
SMILES (Isomeric) CC1(CC2=C(CO1)C(=O)C3=C(C2=O)C=C(C=C3OC)O)O
InChI InChI=1S/C15H14O6/c1-15(19)5-9-10(6-21-15)14(18)12-8(13(9)17)3-7(16)4-11(12)20-2/h3-4,16,19H,5-6H2,1-2H3
InChI Key OHQMZDGELJCFFD-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H14O6
Molecular Weight 290.27 g/mol
Exact Mass 290.07903816 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 0.40
Atomic LogP (AlogP) 1.21
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Desmethylherbarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9894 98.94%
Caco-2 + 0.6718 67.18%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7942 79.42%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.8980 89.80%
OATP1B3 inhibitior + 0.9522 95.22%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8524 85.24%
P-glycoprotein inhibitior - 0.8906 89.06%
P-glycoprotein substrate - 0.8587 85.87%
CYP3A4 substrate + 0.6066 60.66%
CYP2C9 substrate - 0.6092 60.92%
CYP2D6 substrate - 0.8236 82.36%
CYP3A4 inhibition - 0.5719 57.19%
CYP2C9 inhibition - 0.7494 74.94%
CYP2C19 inhibition - 0.6048 60.48%
CYP2D6 inhibition - 0.7463 74.63%
CYP1A2 inhibition + 0.6511 65.11%
CYP2C8 inhibition - 0.6902 69.02%
CYP inhibitory promiscuity - 0.8415 84.15%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9313 93.13%
Carcinogenicity (trinary) Non-required 0.6768 67.68%
Eye corrosion - 0.9845 98.45%
Eye irritation + 0.7693 76.93%
Skin irritation - 0.7718 77.18%
Skin corrosion - 0.9522 95.22%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7426 74.26%
Micronuclear - 0.5400 54.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.7985 79.85%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.8317 83.17%
Acute Oral Toxicity (c) III 0.4403 44.03%
Estrogen receptor binding + 0.8883 88.83%
Androgen receptor binding + 0.6717 67.17%
Thyroid receptor binding - 0.5573 55.73%
Glucocorticoid receptor binding + 0.8749 87.49%
Aromatase binding + 0.5795 57.95%
PPAR gamma + 0.5912 59.12%
Honey bee toxicity - 0.8366 83.66%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5449 54.49%
Fish aquatic toxicity + 0.9864 98.64%

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 97.98% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.54% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.38% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.92% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.44% 89.00%
CHEMBL2581 P07339 Cathepsin D 92.14% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.40% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.25% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.78% 92.94%
CHEMBL4208 P20618 Proteasome component C5 88.10% 90.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.98% 97.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.85% 99.23%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.34% 96.21%
CHEMBL2535 P11166 Glucose transporter 83.01% 98.75%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.77% 91.07%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.49% 97.28%
CHEMBL340 P08684 Cytochrome P450 3A4 81.02% 91.19%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.72% 100.00%

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 46850691
LOTUS LTS0041727
wikiData Q77574189