Trisdechloronornidulin

Details

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Internal ID 00cd6e07-1926-43ac-bde9-44ec30772eff
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name 1-but-2-en-2-yl-3,9-dihydroxy-4,7-dimethylbenzo[b][1,4]benzodioxepin-6-one
SMILES (Canonical) CC=C(C)C1=CC(=C(C2=C1OC3=C(C(=CC(=C3)O)C)C(=O)O2)C)O
SMILES (Isomeric) CC=C(C)C1=CC(=C(C2=C1OC3=C(C(=CC(=C3)O)C)C(=O)O2)C)O
InChI InChI=1S/C19H18O5/c1-5-9(2)13-8-14(21)11(4)17-18(13)23-15-7-12(20)6-10(3)16(15)19(22)24-17/h5-8,20-21H,1-4H3
InChI Key ZPPIKBUIYSSQEH-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18O5
Molecular Weight 326.30 g/mol
Exact Mass 326.11542367 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.46
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Trisdechloronornidulin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9855 98.55%
Caco-2 + 0.8186 81.86%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6401 64.01%
OATP2B1 inhibitior - 0.5764 57.64%
OATP1B1 inhibitior + 0.8034 80.34%
OATP1B3 inhibitior + 0.8402 84.02%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6147 61.47%
P-glycoprotein inhibitior - 0.6951 69.51%
P-glycoprotein substrate - 0.9181 91.81%
CYP3A4 substrate - 0.5364 53.64%
CYP2C9 substrate - 0.5858 58.58%
CYP2D6 substrate - 0.8673 86.73%
CYP3A4 inhibition - 0.7805 78.05%
CYP2C9 inhibition - 0.6272 62.72%
CYP2C19 inhibition + 0.5858 58.58%
CYP2D6 inhibition - 0.8884 88.84%
CYP1A2 inhibition - 0.6848 68.48%
CYP2C8 inhibition + 0.4744 47.44%
CYP inhibitory promiscuity + 0.6183 61.83%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Danger 0.5054 50.54%
Eye corrosion - 0.9909 99.09%
Eye irritation + 0.9175 91.75%
Skin irritation - 0.5968 59.68%
Skin corrosion - 0.9622 96.22%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4803 48.03%
Micronuclear + 0.8300 83.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.6828 68.28%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5618 56.18%
Acute Oral Toxicity (c) II 0.4050 40.50%
Estrogen receptor binding + 0.8367 83.67%
Androgen receptor binding + 0.5998 59.98%
Thyroid receptor binding + 0.6448 64.48%
Glucocorticoid receptor binding + 0.7065 70.65%
Aromatase binding + 0.6637 66.37%
PPAR gamma + 0.7065 70.65%
Honey bee toxicity - 0.8278 82.78%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9935 99.35%

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 97.77% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 95.80% 94.73%
CHEMBL2581 P07339 Cathepsin D 95.67% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.85% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.83% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.76% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.17% 94.00%
CHEMBL2535 P11166 Glucose transporter 85.53% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.12% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.47% 95.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.27% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.16% 99.15%
CHEMBL4040 P28482 MAP kinase ERK2 81.68% 83.82%
CHEMBL1951 P21397 Monoamine oxidase A 81.48% 91.49%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 81.25% 82.38%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.22% 93.40%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.18% 94.42%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 71437316
LOTUS LTS0214518
wikiData Q77501350