(4R,7E,9R,10S,13S,16S)-13-ethoxy-9-hydroxy-4,10,16-trimethyl-1,5,11-trioxacyclohexadec-7-ene-2,6,12,15-tetrone

Details

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Internal ID 6e66d9a6-1536-46ab-939a-d364b310ed85
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (4R,7E,9R,10S,13S,16S)-13-ethoxy-9-hydroxy-4,10,16-trimethyl-1,5,11-trioxacyclohexadec-7-ene-2,6,12,15-tetrone
SMILES (Canonical) CCOC1CC(=O)C(OC(=O)CC(OC(=O)C=CC(C(OC1=O)C)O)C)C
SMILES (Isomeric) CCO[C@H]1CC(=O)[C@@H](OC(=O)C[C@H](OC(=O)/C=C/[C@H]([C@@H](OC1=O)C)O)C)C
InChI InChI=1S/C18H26O9/c1-5-24-15-9-14(20)12(4)26-17(22)8-10(2)25-16(21)7-6-13(19)11(3)27-18(15)23/h6-7,10-13,15,19H,5,8-9H2,1-4H3/b7-6+/t10-,11+,12+,13-,15+/m1/s1
InChI Key FRSLVQFQUNGOIH-DWMWETKCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H26O9
Molecular Weight 386.40 g/mol
Exact Mass 386.15768240 g/mol
Topological Polar Surface Area (TPSA) 125.00 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.47
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4R,7E,9R,10S,13S,16S)-13-ethoxy-9-hydroxy-4,10,16-trimethyl-1,5,11-trioxacyclohexadec-7-ene-2,6,12,15-tetrone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9503 95.03%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7583 75.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8531 85.31%
OATP1B3 inhibitior + 0.8967 89.67%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6219 62.19%
P-glycoprotein inhibitior + 0.5777 57.77%
P-glycoprotein substrate - 0.6008 60.08%
CYP3A4 substrate + 0.5731 57.31%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8924 89.24%
CYP3A4 inhibition - 0.6498 64.98%
CYP2C9 inhibition - 0.8934 89.34%
CYP2C19 inhibition - 0.8369 83.69%
CYP2D6 inhibition - 0.9370 93.70%
CYP1A2 inhibition - 0.8971 89.71%
CYP2C8 inhibition - 0.8387 83.87%
CYP inhibitory promiscuity - 0.9628 96.28%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.6098 60.98%
Eye corrosion - 0.9702 97.02%
Eye irritation - 0.9314 93.14%
Skin irritation - 0.7021 70.21%
Skin corrosion - 0.9615 96.15%
Ames mutagenesis - 0.5754 57.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5428 54.28%
Micronuclear - 0.7126 71.26%
Hepatotoxicity - 0.5051 50.51%
skin sensitisation - 0.7308 73.08%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.7672 76.72%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.6859 68.59%
Acute Oral Toxicity (c) III 0.7277 72.77%
Estrogen receptor binding + 0.5329 53.29%
Androgen receptor binding - 0.5185 51.85%
Thyroid receptor binding - 0.6581 65.81%
Glucocorticoid receptor binding - 0.4843 48.43%
Aromatase binding - 0.8212 82.12%
PPAR gamma - 0.6406 64.06%
Honey bee toxicity - 0.8103 81.03%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5150 51.50%
Fish aquatic toxicity + 0.9415 94.15%

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 94.48% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.27% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.48% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.05% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.43% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.60% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.78% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.53% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 81.32% 94.73%

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 162880368
LOTUS LTS0190116
wikiData Q104952683