Paecilomycin K

Details

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Internal ID 368bca6d-0ac5-4960-bbd9-a809a3c2f1b3
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (1S,2R,11S,13Z,15R,16R)-2,7,15-trihydroxy-5-methoxy-11-methyl-10,19-dioxatricyclo[14.2.1.03,8]nonadeca-3(8),4,6,13-tetraen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H24O7/c1-10-4-3-5-13(20)15-6-7-16(26-15)18(22)12-8-11(24-2)9-14(21)17(12)19(23)25-10/h3,5,8-10,13,15-16,18,20-22H,4,6-7H2,1-2H3/b5-3-/t10-,13+,15+,16-,18+/m0/s1
InChI Key MKEUDCZIYBJFFQ-PCYBLXQVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H24O7
Molecular Weight 364.40 g/mol
Exact Mass 364.15220310 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.85
H-Bond Acceptor 7
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 Paecilomycin K

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9738 97.38%
Caco-2 - 0.6321 63.21%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7620 76.20%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8601 86.01%
OATP1B3 inhibitior + 0.8585 85.85%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8821 88.21%
BSEP inhibitior - 0.5857 58.57%
P-glycoprotein inhibitior - 0.6699 66.99%
P-glycoprotein substrate - 0.8873 88.73%
CYP3A4 substrate + 0.6458 64.58%
CYP2C9 substrate + 0.6036 60.36%
CYP2D6 substrate - 0.8260 82.60%
CYP3A4 inhibition - 0.7280 72.80%
CYP2C9 inhibition - 0.7280 72.80%
CYP2C19 inhibition - 0.5510 55.10%
CYP2D6 inhibition - 0.7102 71.02%
CYP1A2 inhibition + 0.6424 64.24%
CYP2C8 inhibition - 0.5646 56.46%
CYP inhibitory promiscuity - 0.6527 65.27%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Danger 0.4347 43.47%
Eye corrosion - 0.9711 97.11%
Eye irritation - 0.9493 94.93%
Skin irritation - 0.7653 76.53%
Skin corrosion - 0.9320 93.20%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5768 57.68%
Micronuclear - 0.5600 56.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.7352 73.52%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.6840 68.40%
Acute Oral Toxicity (c) I 0.4438 44.38%
Estrogen receptor binding + 0.7530 75.30%
Androgen receptor binding + 0.6499 64.99%
Thyroid receptor binding - 0.6286 62.86%
Glucocorticoid receptor binding + 0.7550 75.50%
Aromatase binding + 0.5321 53.21%
PPAR gamma + 0.7190 71.90%
Honey bee toxicity - 0.8137 81.37%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.8504 85.04%

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 99.38% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.20% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.30% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.97% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.25% 99.15%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 91.62% 91.07%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.23% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.54% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.51% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.01% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.26% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.19% 86.33%
CHEMBL4208 P20618 Proteasome component C5 86.72% 90.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.53% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.13% 89.00%
CHEMBL2581 P07339 Cathepsin D 86.07% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 85.95% 94.73%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 84.38% 82.67%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.31% 99.17%
CHEMBL226 P30542 Adenosine A1 receptor 82.91% 95.93%
CHEMBL340 P08684 Cytochrome P450 3A4 82.39% 91.19%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 82.15% 91.79%
CHEMBL2535 P11166 Glucose transporter 82.12% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.95% 94.45%
CHEMBL4530 P00488 Coagulation factor XIII 81.54% 96.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 81.03% 93.40%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.01% 97.14%

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 71683020
LOTUS LTS0124684
wikiData Q75053129