3-methoxy-6-[(3R,8R)-8-methyl-8-(4-methylpent-3-enyl)-3,4-dihydro-2H-pyrano[2,3-f]chromen-3-yl]benzene-1,2-diol

Details

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Internal ID ed895e20-04d5-4d25-bb8e-80354e194a75
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Pyranoisoflavonoids
IUPAC Name 3-methoxy-6-[(3R,8R)-8-methyl-8-(4-methylpent-3-enyl)-3,4-dihydro-2H-pyrano[2,3-f]chromen-3-yl]benzene-1,2-diol
SMILES (Canonical) CC(=CCCC1(C=CC2=C(O1)C=CC3=C2OCC(C3)C4=C(C(=C(C=C4)OC)O)O)C)C
SMILES (Isomeric) CC(=CCC[C@@]1(C=CC2=C(O1)C=CC3=C2OC[C@H](C3)C4=C(C(=C(C=C4)OC)O)O)C)C
InChI InChI=1S/C26H30O5/c1-16(2)6-5-12-26(3)13-11-20-21(31-26)9-7-17-14-18(15-30-25(17)20)19-8-10-22(29-4)24(28)23(19)27/h6-11,13,18,27-28H,5,12,14-15H2,1-4H3/t18-,26+/m0/s1
InChI Key GRHKVSQNMXZXME-HFJWLAOPSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H30O5
Molecular Weight 422.50 g/mol
Exact Mass 422.20932405 g/mol
Topological Polar Surface Area (TPSA) 68.20 Ų
XlogP 5.80
Atomic LogP (AlogP) 5.74
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-methoxy-6-[(3R,8R)-8-methyl-8-(4-methylpent-3-enyl)-3,4-dihydro-2H-pyrano[2,3-f]chromen-3-yl]benzene-1,2-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9301 93.01%
Caco-2 + 0.5263 52.63%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8225 82.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8400 84.00%
OATP1B3 inhibitior + 0.9152 91.52%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9291 92.91%
P-glycoprotein inhibitior + 0.8099 80.99%
P-glycoprotein substrate + 0.6967 69.67%
CYP3A4 substrate + 0.6951 69.51%
CYP2C9 substrate + 0.5928 59.28%
CYP2D6 substrate + 0.3469 34.69%
CYP3A4 inhibition - 0.8639 86.39%
CYP2C9 inhibition - 0.6531 65.31%
CYP2C19 inhibition - 0.5693 56.93%
CYP2D6 inhibition - 0.8815 88.15%
CYP1A2 inhibition - 0.5323 53.23%
CYP2C8 inhibition + 0.7185 71.85%
CYP inhibitory promiscuity - 0.5753 57.53%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6837 68.37%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.8713 87.13%
Skin irritation - 0.7824 78.24%
Skin corrosion - 0.9476 94.76%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7634 76.34%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8525 85.25%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7831 78.31%
Acute Oral Toxicity (c) III 0.4576 45.76%
Estrogen receptor binding + 0.9276 92.76%
Androgen receptor binding + 0.5975 59.75%
Thyroid receptor binding + 0.7375 73.75%
Glucocorticoid receptor binding + 0.7628 76.28%
Aromatase binding + 0.6534 65.34%
PPAR gamma + 0.8051 80.51%
Honey bee toxicity - 0.7188 71.88%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9815 98.15%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 99.33% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.87% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.01% 96.09%
CHEMBL240 Q12809 HERG 97.37% 89.76%
CHEMBL5608 Q16288 NT-3 growth factor receptor 94.91% 95.89%
CHEMBL2581 P07339 Cathepsin D 94.28% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.48% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.81% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.78% 85.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.25% 92.62%
CHEMBL5555 O00767 Acyl-CoA desaturase 88.16% 97.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.16% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.90% 100.00%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 86.46% 89.05%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 86.39% 96.39%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.32% 89.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 83.54% 94.03%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.23% 100.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.98% 89.62%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.12% 97.14%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.74% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 80.02% 94.73%

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.
Berchemia discolor
Dalbergia nitidula

Cross-Links

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PubChem 162912952
LOTUS LTS0242866
wikiData Q105015928