Lyngbyabellin G

Details

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Internal ID 72f08dc8-7fb7-41cc-91fa-c8aa2fa5b4c6
Taxonomy Organic acids and derivatives > Peptidomimetics > Depsipeptides > Cyclic depsipeptides
IUPAC Name (5R,12S,13S,16S)-12-(4,4-dichloropentyl)-5-hydroxy-16-(2-hydroxypropan-2-yl)-13-methyl-3,11,15-trioxa-7,18-dithia-20,21-diazatricyclo[15.2.1.16,9]henicosa-1(19),6(21),8,17(20)-tetraene-2,10,14-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H28Cl2N2O8S2/c1-11-15(6-5-7-23(4,24)25)34-21(31)13-10-36-17(26-13)14(28)8-33-20(30)12-9-37-18(27-12)16(22(2,3)32)35-19(11)29/h9-11,14-16,28,32H,5-8H2,1-4H3/t11-,14+,15-,16+/m0/s1
InChI Key HPCFVGQULNKVOH-BJKJVOPESA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C23H28Cl2N2O8S2
Molecular Weight 595.50 g/mol
Exact Mass 594.0664136 g/mol
Topological Polar Surface Area (TPSA) 202.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.38
H-Bond Acceptor 12
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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CHEMBL4163844
DTXSID301335249

2D Structure

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2D Structure of Lyngbyabellin G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8815 88.15%
Caco-2 - 0.8063 80.63%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.4475 44.75%
OATP2B1 inhibitior - 0.8572 85.72%
OATP1B1 inhibitior + 0.8942 89.42%
OATP1B3 inhibitior + 0.9272 92.72%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.8392 83.92%
P-glycoprotein inhibitior + 0.7532 75.32%
P-glycoprotein substrate + 0.5309 53.09%
CYP3A4 substrate + 0.6468 64.68%
CYP2C9 substrate - 0.5998 59.98%
CYP2D6 substrate - 0.8636 86.36%
CYP3A4 inhibition - 0.7842 78.42%
CYP2C9 inhibition - 0.7606 76.06%
CYP2C19 inhibition - 0.6370 63.70%
CYP2D6 inhibition - 0.8977 89.77%
CYP1A2 inhibition - 0.6902 69.02%
CYP2C8 inhibition - 0.5616 56.16%
CYP inhibitory promiscuity - 0.9393 93.93%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.4818 48.18%
Eye corrosion - 0.9833 98.33%
Eye irritation - 0.9389 93.89%
Skin irritation - 0.7513 75.13%
Skin corrosion - 0.8953 89.53%
Ames mutagenesis - 0.5654 56.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6659 66.59%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.6801 68.01%
skin sensitisation - 0.8118 81.18%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.4788 47.88%
Acute Oral Toxicity (c) III 0.6169 61.69%
Estrogen receptor binding + 0.6820 68.20%
Androgen receptor binding + 0.6335 63.35%
Thyroid receptor binding + 0.5233 52.33%
Glucocorticoid receptor binding + 0.6195 61.95%
Aromatase binding + 0.6156 61.56%
PPAR gamma + 0.5922 59.22%
Honey bee toxicity - 0.8524 85.24%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.8825 88.25%

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
CHEMBL2581 P07339 Cathepsin D 96.35% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.46% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.42% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 92.34% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.96% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.35% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.36% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.23% 95.56%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 85.12% 100.00%
CHEMBL3891 P07384 Calpain 1 83.70% 93.04%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.13% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.21% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 82.03% 89.63%
CHEMBL226 P30542 Adenosine A1 receptor 81.18% 95.93%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.88% 93.03%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.52% 96.90%

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 11699930
LOTUS LTS0111285
wikiData Q77493633