Plicatilisin G

Details

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Internal ID 9be476cb-58d5-4756-b8ea-4dd7c10374f5
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name (1R,2R,3S,4R,5R,6R,9R,12S)-3,4,12-trihydroxy-6,9-dimethyl-5-propan-2-yl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-13(16)-en-14-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H30O5/c1-9(2)12-15(22)16(23)14-17-13-11(18(24)25-17)10(21)5-6-19(13,3)7-8-20(12,14)4/h9-10,12,14-17,21-23H,5-8H2,1-4H3/t10-,12-,14+,15+,16-,17-,19-,20+/m0/s1
InChI Key ADENOZDDISKJRN-MYZCZZDYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O5
Molecular Weight 350.40 g/mol
Exact Mass 350.20932405 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.79
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Plicatilisin G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9824 98.24%
Caco-2 + 0.5288 52.88%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7556 75.56%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.9112 91.12%
OATP1B3 inhibitior + 0.9323 93.23%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6571 65.71%
BSEP inhibitior - 0.8259 82.59%
P-glycoprotein inhibitior - 0.7578 75.78%
P-glycoprotein substrate - 0.8522 85.22%
CYP3A4 substrate + 0.5890 58.90%
CYP2C9 substrate - 0.8027 80.27%
CYP2D6 substrate - 0.8749 87.49%
CYP3A4 inhibition - 0.7190 71.90%
CYP2C9 inhibition - 0.6026 60.26%
CYP2C19 inhibition - 0.6203 62.03%
CYP2D6 inhibition - 0.9436 94.36%
CYP1A2 inhibition + 0.5273 52.73%
CYP2C8 inhibition - 0.9116 91.16%
CYP inhibitory promiscuity - 0.9479 94.79%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5229 52.29%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9383 93.83%
Skin irritation + 0.5865 58.65%
Skin corrosion - 0.9106 91.06%
Ames mutagenesis - 0.6228 62.28%
Human Ether-a-go-go-Related Gene inhibition - 0.5998 59.98%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.6083 60.83%
skin sensitisation - 0.7797 77.97%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.6546 65.46%
Acute Oral Toxicity (c) I 0.3140 31.40%
Estrogen receptor binding + 0.6873 68.73%
Androgen receptor binding + 0.5994 59.94%
Thyroid receptor binding + 0.6292 62.92%
Glucocorticoid receptor binding + 0.6329 63.29%
Aromatase binding + 0.5701 57.01%
PPAR gamma - 0.5229 52.29%
Honey bee toxicity - 0.7657 76.57%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9868 98.68%

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
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 96.25% 96.38%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.81% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.32% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.66% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.60% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.59% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.27% 99.23%
CHEMBL204 P00734 Thrombin 88.27% 96.01%
CHEMBL221 P23219 Cyclooxygenase-1 86.85% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.49% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.33% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.96% 100.00%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 80.94% 92.88%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.88% 93.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.82% 96.77%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.73% 93.03%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.43% 97.09%

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 102584157
LOTUS LTS0142515
wikiData Q77515750