Racemoflavone

Details

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Internal ID f1ccb467-5963-4a8f-a776-566dc9a7107c
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Pyranoflavonoids
IUPAC Name 5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-8,8-dimethylpyrano[2,3-h]chromen-4-one
SMILES (Canonical) CC1(C=CC2=C(O1)C=C(C3=C2OC(=CC3=O)C4=CC(=C(C=C4)O)OC)O)C
SMILES (Isomeric) CC1(C=CC2=C(O1)C=C(C3=C2OC(=CC3=O)C4=CC(=C(C=C4)O)OC)O)C
InChI InChI=1S/C21H18O6/c1-21(2)7-6-12-17(27-21)10-15(24)19-14(23)9-16(26-20(12)19)11-4-5-13(22)18(8-11)25-3/h4-10,22,24H,1-3H3
InChI Key AGOMJPUUTGWSSH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H18O6
Molecular Weight 366.40 g/mol
Exact Mass 366.11033829 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.06
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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LMPK12110796

2D Structure

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2D Structure of Racemoflavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9825 98.25%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7945 79.45%
OATP2B1 inhibitior - 0.7040 70.40%
OATP1B1 inhibitior + 0.9158 91.58%
OATP1B3 inhibitior + 0.9533 95.33%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7466 74.66%
P-glycoprotein inhibitior + 0.7796 77.96%
P-glycoprotein substrate - 0.7122 71.22%
CYP3A4 substrate + 0.6104 61.04%
CYP2C9 substrate - 0.6192 61.92%
CYP2D6 substrate - 0.8382 83.82%
CYP3A4 inhibition + 0.6259 62.59%
CYP2C9 inhibition - 0.5464 54.64%
CYP2C19 inhibition + 0.8395 83.95%
CYP2D6 inhibition - 0.7544 75.44%
CYP1A2 inhibition - 0.6537 65.37%
CYP2C8 inhibition + 0.7425 74.25%
CYP inhibitory promiscuity + 0.7270 72.70%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Danger 0.4952 49.52%
Eye corrosion - 0.9890 98.90%
Eye irritation + 0.7312 73.12%
Skin irritation - 0.7770 77.70%
Skin corrosion - 0.9581 95.81%
Ames mutagenesis + 0.5472 54.72%
Human Ether-a-go-go-Related Gene inhibition - 0.7016 70.16%
Micronuclear + 0.6900 69.00%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation - 0.8745 87.45%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6671 66.71%
Acute Oral Toxicity (c) III 0.6269 62.69%
Estrogen receptor binding + 0.9423 94.23%
Androgen receptor binding + 0.8397 83.97%
Thyroid receptor binding + 0.7846 78.46%
Glucocorticoid receptor binding + 0.9166 91.66%
Aromatase binding + 0.7331 73.31%
PPAR gamma + 0.8746 87.46%
Honey bee toxicity - 0.7404 74.04%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6149 61.49%
Fish aquatic toxicity + 0.9638 96.38%

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 98.99% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.15% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.02% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.45% 99.15%
CHEMBL2581 P07339 Cathepsin D 93.62% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.20% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.23% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.88% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.14% 85.14%
CHEMBL1907 P15144 Aminopeptidase N 87.53% 93.31%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 85.59% 85.30%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 84.47% 89.23%
CHEMBL3194 P02766 Transthyretin 84.09% 90.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.84% 96.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.00% 97.14%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.99% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.62% 99.17%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.75% 96.77%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.18% 99.23%

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.
Atalantia racemosa
Boswellia papyrifera

Cross-Links

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PubChem 14162622
NPASS NPC82294
LOTUS LTS0166191
wikiData Q104911909