Rhytidchromone E

Details

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Internal ID 5ccb2812-2307-4e02-ba86-aa0c644e2ea8
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name (2R,4S)-4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoic acid
SMILES (Canonical) CC1=CC(=O)C2=C(O1)C(=C(C=C2O)OC)C(CC(C(=O)O)OC)OC
SMILES (Isomeric) CC1=CC(=O)C2=C(O1)C(=C(C=C2O)OC)[C@H](C[C@H](C(=O)O)OC)OC
InChI InChI=1S/C17H20O8/c1-8-5-9(18)14-10(19)6-11(22-2)15(16(14)25-8)12(23-3)7-13(24-4)17(20)21/h5-6,12-13,19H,7H2,1-4H3,(H,20,21)/t12-,13+/m0/s1
InChI Key WFZNCNGLVILQKO-QWHCGFSZSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H20O8
Molecular Weight 352.30 g/mol
Exact Mass 352.11581759 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.99
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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CHEMBL4441862

2D Structure

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2D Structure of Rhytidchromone E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9358 93.58%
Caco-2 + 0.7658 76.58%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6356 63.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8946 89.46%
OATP1B3 inhibitior - 0.2662 26.62%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5612 56.12%
P-glycoprotein inhibitior - 0.7216 72.16%
P-glycoprotein substrate - 0.7209 72.09%
CYP3A4 substrate + 0.5576 55.76%
CYP2C9 substrate + 0.6281 62.81%
CYP2D6 substrate - 0.8789 87.89%
CYP3A4 inhibition - 0.9705 97.05%
CYP2C9 inhibition - 0.9341 93.41%
CYP2C19 inhibition - 0.9341 93.41%
CYP2D6 inhibition - 0.8885 88.85%
CYP1A2 inhibition - 0.5431 54.31%
CYP2C8 inhibition + 0.4621 46.21%
CYP inhibitory promiscuity - 0.8775 87.75%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6999 69.99%
Eye corrosion - 0.9857 98.57%
Eye irritation - 0.7433 74.33%
Skin irritation - 0.8156 81.56%
Skin corrosion - 0.9672 96.72%
Ames mutagenesis - 0.5064 50.64%
Human Ether-a-go-go-Related Gene inhibition - 0.4285 42.85%
Micronuclear + 0.5818 58.18%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.9369 93.69%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.6234 62.34%
Acute Oral Toxicity (c) III 0.5056 50.56%
Estrogen receptor binding + 0.5621 56.21%
Androgen receptor binding + 0.7756 77.56%
Thyroid receptor binding - 0.5695 56.95%
Glucocorticoid receptor binding + 0.5540 55.40%
Aromatase binding - 0.7215 72.15%
PPAR gamma + 0.6416 64.16%
Honey bee toxicity - 0.8875 88.75%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9466 94.66%

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 93.82% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.92% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.37% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.87% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.72% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.19% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 87.70% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.56% 89.00%
CHEMBL3194 P02766 Transthyretin 86.11% 90.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.93% 99.15%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.46% 96.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.68% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.39% 94.45%
CHEMBL1255126 O15151 Protein Mdm4 81.48% 90.20%
CHEMBL4208 P20618 Proteasome component C5 81.35% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.21% 99.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.13% 95.50%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.10% 90.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.77% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.08% 96.00%

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.
There are no matching plants.

Cross-Links

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PubChem 132578879
LOTUS LTS0192584
wikiData Q77497682