Erubescenschromone A

Details

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Internal ID edafc928-07a5-49d8-8ae3-948fa7368d9f
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name (3S)-6,7-dihydroxy-5'-methylspiro[2H-chromene-3,2'-furan]-3',4-dione
SMILES (Canonical) CC1=CC(=O)C2(O1)COC3=CC(=C(C=C3C2=O)O)O
SMILES (Isomeric) CC1=CC(=O)[C@@]2(O1)COC3=CC(=C(C=C3C2=O)O)O
InChI InChI=1S/C13H10O6/c1-6-2-11(16)13(19-6)5-18-10-4-9(15)8(14)3-7(10)12(13)17/h2-4,14-15H,5H2,1H3/t13-/m0/s1
InChI Key JEGHUOLJRQHOKB-ZDUSSCGKSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C13H10O6
Molecular Weight 262.21 g/mol
Exact Mass 262.04773803 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.91
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Erubescenschromone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9748 97.48%
Caco-2 - 0.5574 55.74%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8522 85.22%
OATP2B1 inhibitior - 0.8622 86.22%
OATP1B1 inhibitior + 0.9060 90.60%
OATP1B3 inhibitior + 0.9779 97.79%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8211 82.11%
P-glycoprotein inhibitior - 0.9777 97.77%
P-glycoprotein substrate - 0.8862 88.62%
CYP3A4 substrate + 0.5186 51.86%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8416 84.16%
CYP3A4 inhibition - 0.8242 82.42%
CYP2C9 inhibition + 0.5740 57.40%
CYP2C19 inhibition - 0.5553 55.53%
CYP2D6 inhibition - 0.8801 88.01%
CYP1A2 inhibition + 0.6468 64.68%
CYP2C8 inhibition - 0.8412 84.12%
CYP inhibitory promiscuity - 0.6177 61.77%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4498 44.98%
Eye corrosion - 0.9884 98.84%
Eye irritation + 0.6186 61.86%
Skin irritation - 0.6889 68.89%
Skin corrosion - 0.8836 88.36%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8762 87.62%
Micronuclear + 0.6200 62.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.6468 64.68%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.6241 62.41%
Acute Oral Toxicity (c) III 0.4877 48.77%
Estrogen receptor binding + 0.6695 66.95%
Androgen receptor binding + 0.7331 73.31%
Thyroid receptor binding - 0.5331 53.31%
Glucocorticoid receptor binding + 0.7989 79.89%
Aromatase binding + 0.5664 56.64%
PPAR gamma + 0.5944 59.44%
Honey bee toxicity - 0.8352 83.52%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9168 91.68%

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 98.59% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.25% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.67% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.66% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.72% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.90% 85.14%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.77% 93.40%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.91% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.50% 100.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.21% 94.80%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.60% 96.77%
CHEMBL1951 P21397 Monoamine oxidase A 82.94% 91.49%
CHEMBL4208 P20618 Proteasome component C5 82.54% 90.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.23% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 81.74% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.65% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.91% 99.15%

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 139590707
LOTUS LTS0230894
wikiData Q105126038