23-O-butyrylbafilomycin D

Details

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Internal ID 7b6f4b72-e1b6-4bba-829c-a2f3d29eb5b2
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name [(E,3R,4S,8S,9R,10S)-9-hydroxy-10-[(2R,3S,4E,6E,9R,10S,11R,12E,14Z)-10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl]-2,4,8-trimethyl-7-oxoundec-5-en-3-yl] butanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C39H62O9/c1-13-15-34(41)47-37(23(2)3)26(6)18-19-31(40)29(9)36(43)30(10)38-32(45-11)17-14-16-24(4)20-27(7)35(42)28(8)21-25(5)22-33(46-12)39(44)48-38/h14,16-19,21-23,26-30,32,35-38,42-43H,13,15,20H2,1-12H3/b17-14+,19-18+,24-16+,25-21+,33-22-/t26-,27+,28+,29+,30-,32-,35-,36-,37+,38+/m0/s1
InChI Key MBPAMCVOCHDMNK-CIFCEQHNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C39H62O9
Molecular Weight 674.90 g/mol
Exact Mass 674.43938355 g/mol
Topological Polar Surface Area (TPSA) 129.00 Ų
XlogP 7.20
Atomic LogP (AlogP) 6.69
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 23-O-butyrylbafilomycin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9305 93.05%
Caco-2 - 0.8329 83.29%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7246 72.46%
OATP2B1 inhibitior - 0.5683 56.83%
OATP1B1 inhibitior + 0.8203 82.03%
OATP1B3 inhibitior + 0.9260 92.60%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9486 94.86%
P-glycoprotein inhibitior + 0.7878 78.78%
P-glycoprotein substrate + 0.7306 73.06%
CYP3A4 substrate + 0.6824 68.24%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9032 90.32%
CYP3A4 inhibition - 0.7435 74.35%
CYP2C9 inhibition - 0.7795 77.95%
CYP2C19 inhibition - 0.6056 60.56%
CYP2D6 inhibition - 0.8972 89.72%
CYP1A2 inhibition - 0.8715 87.15%
CYP2C8 inhibition + 0.7397 73.97%
CYP inhibitory promiscuity - 0.9211 92.11%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8002 80.02%
Carcinogenicity (trinary) Non-required 0.5964 59.64%
Eye corrosion - 0.9696 96.96%
Eye irritation - 0.9150 91.50%
Skin irritation - 0.7511 75.11%
Skin corrosion - 0.9458 94.58%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4006 40.06%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.5073 50.73%
skin sensitisation - 0.7755 77.55%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.8598 85.98%
Acute Oral Toxicity (c) III 0.6004 60.04%
Estrogen receptor binding + 0.7365 73.65%
Androgen receptor binding + 0.5457 54.57%
Thyroid receptor binding + 0.5132 51.32%
Glucocorticoid receptor binding + 0.7691 76.91%
Aromatase binding + 0.5617 56.17%
PPAR gamma + 0.6809 68.09%
Honey bee toxicity - 0.6408 64.08%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.7904 79.04%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.67% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.60% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.42% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.66% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.29% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.82% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 92.29% 93.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.95% 86.33%
CHEMBL2535 P11166 Glucose transporter 91.79% 98.75%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 90.96% 94.80%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.77% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.04% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 89.00% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.06% 97.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.99% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.30% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.39% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 85.10% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.08% 96.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.84% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.45% 90.71%

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 156581574
LOTUS LTS0216490
wikiData Q105160880