Gancaonin S

Details

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Internal ID 4fed32ef-7978-4be3-bd43-372231dfbb31
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 5-[2-(3,4-dihydroxyphenyl)ethyl]-2,4-bis(3-methylbut-2-enyl)benzene-1,3-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H30O4/c1-15(2)5-10-19-18(9-7-17-8-12-21(25)23(27)13-17)14-22(26)20(24(19)28)11-6-16(3)4/h5-6,8,12-14,25-28H,7,9-11H2,1-4H3
InChI Key VLJOWGMLRJTNDQ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C24H30O4
Molecular Weight 382.50 g/mol
Exact Mass 382.21440943 g/mol
Topological Polar Surface Area (TPSA) 80.90 Ų
XlogP 6.60
Atomic LogP (AlogP) 5.31
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 7

Synonyms

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134958-54-6
4-(2-(2,4-Bis((2E)-3-methylbut-2-enyl)-3,5-dihydroxyphenyl)ethyl)benzene-1,2-diol
DTXSID30159156
5-[2-(3,4-dihydroxyphenyl)ethyl]-2,4-bis(3-methylbut-2-enyl)benzene-1,3-diol
4-{2-[2,4-Bis((2E)-3-methylbut-2-enyl)-3,5-dihydroxyphenyl]ethyl}benzene-1,2-diol
5-(2-(3,4-dihydroxyphenyl)ethyl)-2,4-bis(3-methylbut-2-enyl)benzene-1,3-diol
RefChem:142385
DTXCID9081647
SCHEMBL22579982
SCHEMBL30499856

2D Structure

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2D Structure of Gancaonin S

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9588 95.88%
Caco-2 + 0.4901 49.01%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8218 82.18%
OATP2B1 inhibitior - 0.5625 56.25%
OATP1B1 inhibitior + 0.8973 89.73%
OATP1B3 inhibitior + 0.9310 93.10%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9389 93.89%
P-glycoprotein inhibitior + 0.7132 71.32%
P-glycoprotein substrate - 0.8234 82.34%
CYP3A4 substrate - 0.5631 56.31%
CYP2C9 substrate - 0.7912 79.12%
CYP2D6 substrate + 0.3482 34.82%
CYP3A4 inhibition - 0.5879 58.79%
CYP2C9 inhibition + 0.7343 73.43%
CYP2C19 inhibition + 0.6640 66.40%
CYP2D6 inhibition - 0.7140 71.40%
CYP1A2 inhibition + 0.7232 72.32%
CYP2C8 inhibition - 0.6725 67.25%
CYP inhibitory promiscuity + 0.6619 66.19%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8623 86.23%
Carcinogenicity (trinary) Non-required 0.7430 74.30%
Eye corrosion - 0.9863 98.63%
Eye irritation + 0.5615 56.15%
Skin irritation - 0.7580 75.80%
Skin corrosion - 0.8455 84.55%
Ames mutagenesis - 0.5354 53.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7717 77.17%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.6947 69.47%
skin sensitisation - 0.5554 55.54%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.8481 84.81%
Acute Oral Toxicity (c) III 0.6334 63.34%
Estrogen receptor binding + 0.9298 92.98%
Androgen receptor binding + 0.8958 89.58%
Thyroid receptor binding + 0.7692 76.92%
Glucocorticoid receptor binding + 0.7785 77.85%
Aromatase binding + 0.7416 74.16%
PPAR gamma + 0.9202 92.02%
Honey bee toxicity - 0.8012 80.12%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 1.0000 100.00%

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 99.36% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.30% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 93.69% 91.49%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 92.97% 95.17%
CHEMBL3401 O75469 Pregnane X receptor 92.17% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.20% 94.45%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 87.67% 92.68%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.85% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.52% 96.95%
CHEMBL4208 P20618 Proteasome component C5 84.02% 90.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.39% 90.24%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.16% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.84% 99.17%
CHEMBL3194 P02766 Transthyretin 81.35% 90.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.10% 99.15%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 80.75% 83.57%

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.
Glycyrrhiza
Glycyrrhiza uralensis
Glycyrrhiza uralensis
Mitracarpus hirtus

Cross-Links

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PubChem 480816
NPASS NPC147696
LOTUS LTS0263003
wikiData Q83027474