2-(3,5-dimethoxyphenyl)-6-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromene-5,7-diol

Details

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Internal ID 40e598cb-72e9-4ea8-8ff7-5d46b18b20f9
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 6-prenylated flavans
IUPAC Name 2-(3,5-dimethoxyphenyl)-6-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromene-5,7-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H26O5/c1-13(2)5-6-17-19(23)12-21-18(22(17)24)7-8-20(27-21)14-9-15(25-3)11-16(10-14)26-4/h5,9-12,20,23-24H,6-8H2,1-4H3
InChI Key LLRPPTLVKGWPCU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26O5
Molecular Weight 370.40 g/mol
Exact Mass 370.17802393 g/mol
Topological Polar Surface Area (TPSA) 68.20 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.69
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 2-(3,5-dimethoxyphenyl)-6-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromene-5,7-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9673 96.73%
Caco-2 + 0.5959 59.59%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7659 76.59%
OATP2B1 inhibitior - 0.8621 86.21%
OATP1B1 inhibitior + 0.8561 85.61%
OATP1B3 inhibitior + 0.9255 92.55%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.8554 85.54%
P-glycoprotein inhibitior + 0.7306 73.06%
P-glycoprotein substrate - 0.8367 83.67%
CYP3A4 substrate + 0.5629 56.29%
CYP2C9 substrate - 0.6075 60.75%
CYP2D6 substrate + 0.5000 50.00%
CYP3A4 inhibition - 0.6502 65.02%
CYP2C9 inhibition + 0.5584 55.84%
CYP2C19 inhibition + 0.7769 77.69%
CYP2D6 inhibition - 0.5600 56.00%
CYP1A2 inhibition + 0.7972 79.72%
CYP2C8 inhibition - 0.5761 57.61%
CYP inhibitory promiscuity + 0.8966 89.66%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.7473 74.73%
Eye corrosion - 0.9885 98.85%
Eye irritation + 0.5322 53.22%
Skin irritation - 0.7956 79.56%
Skin corrosion - 0.9345 93.45%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8561 85.61%
Micronuclear - 0.6300 63.00%
Hepatotoxicity - 0.6726 67.26%
skin sensitisation - 0.8276 82.76%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.9279 92.79%
Acute Oral Toxicity (c) III 0.4491 44.91%
Estrogen receptor binding + 0.8609 86.09%
Androgen receptor binding + 0.6690 66.90%
Thyroid receptor binding + 0.7675 76.75%
Glucocorticoid receptor binding + 0.7423 74.23%
Aromatase binding + 0.5361 53.61%
PPAR gamma + 0.8951 89.51%
Honey bee toxicity - 0.8779 87.79%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9768 97.68%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.59% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.82% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.87% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.59% 94.45%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 91.07% 92.68%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.36% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.57% 92.94%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 88.49% 93.40%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.44% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.92% 99.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.91% 92.62%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.04% 93.99%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.61% 86.92%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.62% 99.15%
CHEMBL3438 Q05513 Protein kinase C zeta 84.60% 88.48%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.65% 95.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.55% 95.89%
CHEMBL1951 P21397 Monoamine oxidase A 83.30% 91.49%
CHEMBL4208 P20618 Proteasome component C5 81.26% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.91% 86.33%
CHEMBL2581 P07339 Cathepsin D 80.75% 98.95%
CHEMBL1929 P47989 Xanthine dehydrogenase 80.06% 96.12%

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.
Cyperus conglomeratus

Cross-Links

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PubChem 10832955
LOTUS LTS0038898
wikiData Q105153688