Macrolactin O

Details

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Internal ID 168f2471-7865-423d-b5fc-e30a7d88bfac
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (3Z,5E,8S,9E,11Z,14S,19E,24R)-14-hydroxy-24-methyl-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-oxacyclotetracosa-3,5,9,11,19-pentaene-2,16-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H44O10/c1-21-13-7-3-2-4-8-14-22(32)19-23(33)15-9-5-10-16-24(17-11-6-12-18-26(34)38-21)39-30-29(37)28(36)27(35)25(20-31)40-30/h2,4-6,9-12,16,18,21,23-25,27-31,33,35-37H,3,7-8,13-15,17,19-20H2,1H3/b4-2+,9-5-,11-6+,16-10+,18-12-/t21-,23+,24-,25-,27-,28+,29-,30-/m1/s1
InChI Key WPGAONUYAGVAII-BEAZUXIFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H44O10
Molecular Weight 564.70 g/mol
Exact Mass 564.29344760 g/mol
Topological Polar Surface Area (TPSA) 163.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 1.95
H-Bond Acceptor 10
H-Bond Donor 5
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Macrolactin O

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7485 74.85%
Caco-2 - 0.8669 86.69%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.8571 85.71%
Subcellular localzation Mitochondria 0.8722 87.22%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8447 84.47%
OATP1B3 inhibitior + 0.9104 91.04%
MATE1 inhibitior - 0.9012 90.12%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.8503 85.03%
P-glycoprotein inhibitior + 0.6101 61.01%
P-glycoprotein substrate - 0.6406 64.06%
CYP3A4 substrate + 0.6746 67.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8940 89.40%
CYP3A4 inhibition - 0.8071 80.71%
CYP2C9 inhibition - 0.9343 93.43%
CYP2C19 inhibition - 0.9068 90.68%
CYP2D6 inhibition - 0.9347 93.47%
CYP1A2 inhibition - 0.9031 90.31%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.9872 98.72%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7813 78.13%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.9422 94.22%
Skin irritation - 0.7333 73.33%
Skin corrosion - 0.9615 96.15%
Ames mutagenesis - 0.6270 62.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7917 79.17%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.7771 77.71%
skin sensitisation - 0.9131 91.31%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6708 67.08%
Acute Oral Toxicity (c) III 0.6065 60.65%
Estrogen receptor binding + 0.7157 71.57%
Androgen receptor binding + 0.5754 57.54%
Thyroid receptor binding - 0.6288 62.88%
Glucocorticoid receptor binding - 0.4802 48.02%
Aromatase binding - 0.5844 58.44%
PPAR gamma + 0.5215 52.15%
Honey bee toxicity - 0.7486 74.86%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.8451 84.51%

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 98.58% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.85% 98.95%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 94.41% 96.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.79% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.48% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.17% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.81% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.45% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.83% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.30% 86.33%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.61% 91.07%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.44% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 83.07% 92.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.03% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.26% 99.23%

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 23655941
LOTUS LTS0270476
wikiData Q77419887