Svetamycin A

Details

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Internal ID c10ef9eb-ff19-4f95-8f4c-87dbe275f6ae
Taxonomy Organic acids and derivatives > Peptidomimetics > Depsipeptides > Cyclic depsipeptides
IUPAC Name (3R,5S,10S,13S,14S,15R,23S,26S)-5-chloro-14,15-dihydroxy-23-(hydroxymethyl)-10,23-dimethyl-21-oxa-1,7,8,11,17,18,24,30-octazatetracyclo[24.4.0.03,8.013,18]triacont-16-ene-2,9,12,19,22,25-hexone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H35ClN8O10/c1-11-21(40)32-14(6-12(25)7-27-32)22(41)31-13(4-3-5-26-31)19(38)30-24(2,10-34)23(42)43-9-16(36)33-17(20(39)29-11)18(37)15(35)8-28-33/h8,11-15,17-18,26-27,34-35,37H,3-7,9-10H2,1-2H3,(H,29,39)(H,30,38)/t11-,12-,13-,14+,15+,17-,18+,24-/m0/s1
InChI Key AKKGAIKLKJWDBP-WECLKIJSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H35ClN8O10
Molecular Weight 631.00 g/mol
Exact Mass 630.2164670 g/mol
Topological Polar Surface Area (TPSA) 243.00 Ų
XlogP -3.10
Atomic LogP (AlogP) -4.96
H-Bond Acceptor 13
H-Bond Donor 7
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Svetamycin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7148 71.48%
Caco-2 - 0.8615 86.15%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5246 52.46%
OATP2B1 inhibitior - 0.7146 71.46%
OATP1B1 inhibitior + 0.8135 81.35%
OATP1B3 inhibitior + 0.9323 93.23%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9218 92.18%
P-glycoprotein inhibitior + 0.6368 63.68%
P-glycoprotein substrate + 0.7177 71.77%
CYP3A4 substrate + 0.7118 71.18%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8423 84.23%
CYP3A4 inhibition - 0.9037 90.37%
CYP2C9 inhibition - 0.7581 75.81%
CYP2C19 inhibition - 0.6570 65.70%
CYP2D6 inhibition - 0.8659 86.59%
CYP1A2 inhibition - 0.7843 78.43%
CYP2C8 inhibition + 0.5875 58.75%
CYP inhibitory promiscuity - 0.9350 93.50%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.4558 45.58%
Eye corrosion - 0.9802 98.02%
Eye irritation - 0.9330 93.30%
Skin irritation - 0.7619 76.19%
Skin corrosion - 0.9198 91.98%
Ames mutagenesis + 0.5152 51.52%
Human Ether-a-go-go-Related Gene inhibition - 0.5690 56.90%
Micronuclear + 0.8700 87.00%
Hepatotoxicity + 0.6053 60.53%
skin sensitisation - 0.8181 81.81%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity + 0.6754 67.54%
Acute Oral Toxicity (c) III 0.5787 57.87%
Estrogen receptor binding + 0.7243 72.43%
Androgen receptor binding + 0.6777 67.77%
Thyroid receptor binding + 0.5716 57.16%
Glucocorticoid receptor binding + 0.6236 62.36%
Aromatase binding + 0.6515 65.15%
PPAR gamma + 0.6334 63.34%
Honey bee toxicity - 0.7502 75.02%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity - 0.4871 48.71%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.04% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 96.31% 97.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.34% 96.77%
CHEMBL2581 P07339 Cathepsin D 94.00% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.84% 94.45%
CHEMBL5103 Q969S8 Histone deacetylase 10 89.83% 90.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.79% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.66% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.53% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.49% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.19% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.80% 99.23%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.60% 86.00%
CHEMBL228 P31645 Serotonin transporter 82.91% 95.51%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.86% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.47% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.90% 95.89%
CHEMBL3310 Q96DB2 Histone deacetylase 11 80.86% 88.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.23% 89.00%

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 139591392
LOTUS LTS0018634
wikiData Q104913686