Prosogerin A

Details

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Internal ID 5cee8af4-0227-437b-a9a1-50b69d36f5f6
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 6-O-methylated flavonoids
IUPAC Name 2-(1,3-benzodioxol-5-yl)-7-hydroxy-6-methoxychromen-4-one
SMILES (Canonical) COC1=C(C=C2C(=C1)C(=O)C=C(O2)C3=CC4=C(C=C3)OCO4)O
SMILES (Isomeric) COC1=C(C=C2C(=C1)C(=O)C=C(O2)C3=CC4=C(C=C3)OCO4)O
InChI InChI=1S/C17H12O6/c1-20-16-5-10-11(18)6-14(23-15(10)7-12(16)19)9-2-3-13-17(4-9)22-8-21-13/h2-7,19H,8H2,1H3
InChI Key MAKXJHCYKKCQQY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H12O6
Molecular Weight 312.27 g/mol
Exact Mass 312.06338810 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.90
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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LMPK12110068

2D Structure

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2D Structure of Prosogerin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9849 98.49%
Caco-2 + 0.7797 77.97%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.8138 81.38%
OATP2B1 inhibitior - 0.8614 86.14%
OATP1B1 inhibitior + 0.9573 95.73%
OATP1B3 inhibitior + 0.9711 97.11%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5177 51.77%
P-glycoprotein inhibitior + 0.6660 66.60%
P-glycoprotein substrate - 0.8792 87.92%
CYP3A4 substrate + 0.5329 53.29%
CYP2C9 substrate - 0.8253 82.53%
CYP2D6 substrate - 0.8058 80.58%
CYP3A4 inhibition + 0.8527 85.27%
CYP2C9 inhibition + 0.8760 87.60%
CYP2C19 inhibition + 0.8680 86.80%
CYP2D6 inhibition + 0.6119 61.19%
CYP1A2 inhibition - 0.5473 54.73%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.8201 82.01%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4163 41.63%
Eye corrosion - 0.9811 98.11%
Eye irritation - 0.5937 59.37%
Skin irritation - 0.7070 70.70%
Skin corrosion - 0.9649 96.49%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7328 73.28%
Micronuclear + 0.8674 86.74%
Hepatotoxicity - 0.7385 73.85%
skin sensitisation - 0.8283 82.83%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6970 69.70%
Acute Oral Toxicity (c) III 0.6682 66.82%
Estrogen receptor binding + 0.9524 95.24%
Androgen receptor binding + 0.8344 83.44%
Thyroid receptor binding + 0.6404 64.04%
Glucocorticoid receptor binding + 0.8909 89.09%
Aromatase binding + 0.8014 80.14%
PPAR gamma + 0.8451 84.51%
Honey bee toxicity - 0.8414 84.14%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6149 61.49%
Fish aquatic toxicity + 0.9082 90.82%

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 99.14% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.13% 85.14%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 97.73% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.33% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.49% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.22% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.11% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.98% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.00% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.83% 99.15%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.23% 92.62%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 86.01% 82.67%
CHEMBL1907 P15144 Aminopeptidase N 85.01% 93.31%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 84.90% 80.96%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 84.05% 85.30%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.82% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.78% 93.99%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 83.20% 93.24%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.80% 90.71%
CHEMBL2535 P11166 Glucose transporter 81.61% 98.75%
CHEMBL3438 Q05513 Protein kinase C zeta 80.84% 88.48%

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.
Prosopis cineraria

Cross-Links

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PubChem 44257586
LOTUS LTS0067112
wikiData Q105160391