Scorzocreticin

Details

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Internal ID 4232d904-ace0-48ca-adc8-029577868fe4
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Hydroxybenzoic acid derivatives
IUPAC Name (3S)-6,8-dihydroxy-3-(4-methoxyphenyl)-3,4-dihydroisochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H14O5/c1-20-12-4-2-9(3-5-12)14-7-10-6-11(17)8-13(18)15(10)16(19)21-14/h2-6,8,14,17-18H,7H2,1H3/t14-/m0/s1
InChI Key YDKSIUTUSDFNRH-AWEZNQCLSA-N
Popularity 3 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) 76.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.56
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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(3S)-6,8-dihydroxy-3-(4-methoxyphenyl)-3,4-dihydroisochromen-1-one

2D Structure

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2D Structure of Scorzocreticin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9175 91.75%
Caco-2 + 0.6724 67.24%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7653 76.53%
OATP2B1 inhibitior - 0.7352 73.52%
OATP1B1 inhibitior + 0.9043 90.43%
OATP1B3 inhibitior + 0.9633 96.33%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7904 79.04%
P-glycoprotein inhibitior - 0.8398 83.98%
P-glycoprotein substrate - 0.9450 94.50%
CYP3A4 substrate + 0.6017 60.17%
CYP2C9 substrate - 0.5444 54.44%
CYP2D6 substrate - 0.7993 79.93%
CYP3A4 inhibition + 0.7145 71.45%
CYP2C9 inhibition + 0.8464 84.64%
CYP2C19 inhibition + 0.7522 75.22%
CYP2D6 inhibition - 0.5284 52.84%
CYP1A2 inhibition + 0.7825 78.25%
CYP2C8 inhibition - 0.6244 62.44%
CYP inhibitory promiscuity + 0.6696 66.96%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5459 54.59%
Eye corrosion - 0.9832 98.32%
Eye irritation + 0.8023 80.23%
Skin irritation - 0.7038 70.38%
Skin corrosion - 0.9498 94.98%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5648 56.48%
Micronuclear + 0.8159 81.59%
Hepatotoxicity - 0.6093 60.93%
skin sensitisation - 0.9520 95.20%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5898 58.98%
Acute Oral Toxicity (c) III 0.4975 49.75%
Estrogen receptor binding + 0.7474 74.74%
Androgen receptor binding + 0.7974 79.74%
Thyroid receptor binding + 0.6920 69.20%
Glucocorticoid receptor binding + 0.7329 73.29%
Aromatase binding + 0.6835 68.35%
PPAR gamma + 0.7403 74.03%
Honey bee toxicity - 0.9135 91.35%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.7858 78.58%

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 98.94% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.86% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.01% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.17% 96.09%
CHEMBL4208 P20618 Proteasome component C5 92.20% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.25% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.84% 99.15%
CHEMBL2581 P07339 Cathepsin D 90.82% 98.95%
CHEMBL1929 P47989 Xanthine dehydrogenase 89.74% 96.12%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.33% 93.99%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.05% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.63% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 86.77% 91.49%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.20% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.99% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.86% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.20% 85.14%
CHEMBL2535 P11166 Glucose transporter 82.37% 98.75%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.63% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.57% 92.62%
CHEMBL3401 O75469 Pregnane X receptor 81.44% 94.73%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.10% 97.14%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.09% 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.
Gelasia cretica

Cross-Links

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PubChem 10913129
LOTUS LTS0047873
wikiData Q105346789