Stipulin

Details

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Internal ID 8fcec099-7907-4c74-9363-21555994f03e
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > 3-prenylated chalcones
IUPAC Name (E)-1-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]prop-2-en-1-one
SMILES (Canonical) CC(=CCC1=CC(=C(C=C1O)O)C(=O)C=CC2=CC(=C(C=C2)O)CC=C(C)C)C
SMILES (Isomeric) CC(=CCC1=CC(=C(C=C1O)O)C(=O)/C=C/C2=CC(=C(C=C2)O)CC=C(C)C)C
InChI InChI=1S/C25H28O4/c1-16(2)5-9-19-13-18(7-11-22(19)26)8-12-23(27)21-14-20(10-6-17(3)4)24(28)15-25(21)29/h5-8,11-15,26,28-29H,9-10H2,1-4H3/b12-8+
InChI Key UENVXGIVHQSJHZ-XYOKQWHBSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C25H28O4
Molecular Weight 392.50 g/mol
Exact Mass 392.19875937 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 7.00
Atomic LogP (AlogP) 5.72
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

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SCHEMBL633709
CHEMBL1169874
LMPK12120060
(E)-1-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]prop-2-en-1-one
1-[2,4-Dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]prop-2-en-1-one

2D Structure

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2D Structure of Stipulin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.4938 49.38%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7934 79.34%
OATP2B1 inhibitior + 0.5695 56.95%
OATP1B1 inhibitior + 0.9473 94.73%
OATP1B3 inhibitior + 0.9138 91.38%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9264 92.64%
P-glycoprotein inhibitior + 0.6722 67.22%
P-glycoprotein substrate - 0.8855 88.55%
CYP3A4 substrate - 0.6269 62.69%
CYP2C9 substrate - 0.7861 78.61%
CYP2D6 substrate - 0.8509 85.09%
CYP3A4 inhibition + 0.5746 57.46%
CYP2C9 inhibition + 0.9246 92.46%
CYP2C19 inhibition + 0.9412 94.12%
CYP2D6 inhibition - 0.7114 71.14%
CYP1A2 inhibition + 0.9313 93.13%
CYP2C8 inhibition - 0.7356 73.56%
CYP inhibitory promiscuity + 0.9233 92.33%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7872 78.72%
Carcinogenicity (trinary) Non-required 0.7577 75.77%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.6526 65.26%
Skin irritation - 0.7601 76.01%
Skin corrosion - 0.9035 90.35%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8357 83.57%
Micronuclear - 0.5700 57.00%
Hepatotoxicity - 0.5718 57.18%
skin sensitisation + 0.6235 62.35%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6654 66.54%
Acute Oral Toxicity (c) III 0.7107 71.07%
Estrogen receptor binding + 0.9289 92.89%
Androgen receptor binding + 0.8396 83.96%
Thyroid receptor binding + 0.7345 73.45%
Glucocorticoid receptor binding + 0.8787 87.87%
Aromatase binding + 0.7989 79.89%
PPAR gamma + 0.9058 90.58%
Honey bee toxicity - 0.9271 92.71%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.7300 73.00%
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 98.90% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.89% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.60% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 90.93% 94.73%
CHEMBL1929 P47989 Xanthine dehydrogenase 90.51% 96.12%
CHEMBL2581 P07339 Cathepsin D 90.37% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.89% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.29% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 86.65% 91.49%
CHEMBL3194 P02766 Transthyretin 86.19% 90.71%
CHEMBL221 P23219 Cyclooxygenase-1 85.12% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.55% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.34% 99.17%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.91% 91.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.28% 95.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.30% 89.00%
CHEMBL2535 P11166 Glucose transporter 80.96% 98.75%

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.
Dalbergia stipulacea
Dorstenia barteri
Dorstenia dinklagei
Dorstenia kameruniana

Cross-Links

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PubChem 10069091
LOTUS LTS0104411
wikiData Q104399028