Sakisacaulon A

Details

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Internal ID cb67bfe6-933a-428c-9846-ede4a68c2b5e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Diarylethers
IUPAC Name 3-butyl-7-(2,4-dihydroxy-6-pentylphenoxy)-3-hydroxy-5-methoxy-2-benzofuran-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H30O7/c1-4-6-8-9-15-11-16(25)12-19(26)22(15)30-20-14-17(29-3)13-18-21(20)23(27)31-24(18,28)10-7-5-2/h11-14,25-26,28H,4-10H2,1-3H3
InChI Key PDZXHKSZUJKQQU-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C24H30O7
Molecular Weight 430.50 g/mol
Exact Mass 430.19915329 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 5.60
Atomic LogP (AlogP) 5.14
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 10

Synonyms

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CHEMBL563581
SCHEMBL17301646
BDBM50340636

2D Structure

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2D Structure of Sakisacaulon A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9525 95.25%
Caco-2 - 0.5766 57.66%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.6088 60.88%
OATP2B1 inhibitior - 0.7200 72.00%
OATP1B1 inhibitior + 0.8341 83.41%
OATP1B3 inhibitior + 0.7880 78.80%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9399 93.99%
P-glycoprotein inhibitior + 0.7704 77.04%
P-glycoprotein substrate - 0.6179 61.79%
CYP3A4 substrate + 0.6558 65.58%
CYP2C9 substrate - 0.5962 59.62%
CYP2D6 substrate - 0.7992 79.92%
CYP3A4 inhibition + 0.6878 68.78%
CYP2C9 inhibition - 0.6994 69.94%
CYP2C19 inhibition - 0.7251 72.51%
CYP2D6 inhibition - 0.8883 88.83%
CYP1A2 inhibition - 0.5171 51.71%
CYP2C8 inhibition + 0.8339 83.39%
CYP inhibitory promiscuity - 0.5690 56.90%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5988 59.88%
Eye corrosion - 0.9925 99.25%
Eye irritation - 0.7073 70.73%
Skin irritation - 0.6988 69.88%
Skin corrosion - 0.9193 91.93%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3869 38.69%
Micronuclear - 0.7500 75.00%
Hepatotoxicity - 0.6143 61.43%
skin sensitisation - 0.8844 88.44%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.7624 76.24%
Acute Oral Toxicity (c) II 0.3850 38.50%
Estrogen receptor binding + 0.7966 79.66%
Androgen receptor binding + 0.6792 67.92%
Thyroid receptor binding + 0.5438 54.38%
Glucocorticoid receptor binding + 0.8108 81.08%
Aromatase binding + 0.7419 74.19%
PPAR gamma + 0.8223 82.23%
Honey bee toxicity - 0.8932 89.32%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6461 64.61%
Fish aquatic toxicity + 0.9895 98.95%

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
CHEMBL240 Q12809 HERG 99.74% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.49% 91.11%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 96.60% 95.17%
CHEMBL2581 P07339 Cathepsin D 95.25% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.59% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.56% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.22% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.01% 95.56%
CHEMBL4208 P20618 Proteasome component C5 91.94% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.40% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.94% 94.00%
CHEMBL230 P35354 Cyclooxygenase-2 88.59% 89.63%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.01% 92.62%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.94% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 87.49% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.41% 93.99%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.67% 96.95%
CHEMBL2535 P11166 Glucose transporter 83.25% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.68% 99.23%
CHEMBL1907 P15144 Aminopeptidase N 82.07% 93.31%
CHEMBL1929 P47989 Xanthine dehydrogenase 80.95% 96.12%

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 45273035
LOTUS LTS0121541
wikiData Q77506440