Flavasperone

Details

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Internal ID ab2bb9b5-f3a3-4bd3-9a94-b6bcb44c7842
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
IUPAC Name 5-hydroxy-8,10-dimethoxy-2-methylbenzo[h]chromen-4-one
SMILES (Canonical) CC1=CC(=O)C2=C(O1)C3=C(C=C(C=C3C=C2O)OC)OC
SMILES (Isomeric) CC1=CC(=O)C2=C(O1)C3=C(C=C(C=C3C=C2O)OC)OC
InChI InChI=1S/C16H14O5/c1-8-4-11(17)15-12(18)6-9-5-10(19-2)7-13(20-3)14(9)16(15)21-8/h4-7,18H,1-3H3
InChI Key ARXPDHLVDOYIPX-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O5
Molecular Weight 286.28 g/mol
Exact Mass 286.08412354 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.98
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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Asperxanthon
ASPERXANTHONE
3566-99-2
QUS3F7KQ3E
Antibiotic TMC 256c2
UNII-QUS3F7KQ3E
TMC 256c2
4H-Naphtho(1,2-b)pyran-4-one, 5-hydroxy-8,10-dimethoxy-2-methyl-
Flavasperon
5-hydroxy-8,10-dimethoxy-2-methyl-4H-naphtho[1,2-b]pyran-4-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Flavasperone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9841 98.41%
Caco-2 + 0.8442 84.42%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6678 66.78%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.9300 93.00%
OATP1B3 inhibitior + 0.9873 98.73%
MATE1 inhibitior - 0.6000 60.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6833 68.33%
P-glycoprotein inhibitior - 0.5323 53.23%
P-glycoprotein substrate - 0.8901 89.01%
CYP3A4 substrate + 0.5144 51.44%
CYP2C9 substrate - 0.6360 63.60%
CYP2D6 substrate - 0.8410 84.10%
CYP3A4 inhibition + 0.5994 59.94%
CYP2C9 inhibition - 0.9188 91.88%
CYP2C19 inhibition - 0.6082 60.82%
CYP2D6 inhibition - 0.8535 85.35%
CYP1A2 inhibition + 0.9359 93.59%
CYP2C8 inhibition - 0.7396 73.96%
CYP inhibitory promiscuity - 0.6092 60.92%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9113 91.13%
Carcinogenicity (trinary) Non-required 0.5650 56.50%
Eye corrosion - 0.9482 94.82%
Eye irritation + 0.7854 78.54%
Skin irritation - 0.7107 71.07%
Skin corrosion - 0.9915 99.15%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5210 52.10%
Micronuclear + 0.8200 82.00%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation - 0.9602 96.02%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.5443 54.43%
Acute Oral Toxicity (c) III 0.5893 58.93%
Estrogen receptor binding + 0.8119 81.19%
Androgen receptor binding + 0.7308 73.08%
Thyroid receptor binding + 0.6153 61.53%
Glucocorticoid receptor binding + 0.7167 71.67%
Aromatase binding + 0.8290 82.90%
PPAR gamma + 0.8401 84.01%
Honey bee toxicity - 0.8795 87.95%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.7667 76.67%

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
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.13% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.45% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.45% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.12% 99.15%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.00% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 88.46% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.24% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.22% 99.17%
CHEMBL4208 P20618 Proteasome component C5 84.75% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.70% 86.33%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.29% 93.65%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.81% 85.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.10% 92.94%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.78% 95.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.81% 89.00%
CHEMBL2535 P11166 Glucose transporter 80.61% 98.75%
CHEMBL2581 P07339 Cathepsin D 80.36% 98.95%

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 5748546
LOTUS LTS0007881
wikiData Q77375969