15-[(4,5-Dihydroxy-3-methoxy-6-methyloxan-2-yl)oxymethyl]-6-[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-16-ethyl-5,7,9-trimethyl-1-oxacyclohexadeca-3,11,13-triene-2,10-dione

Details

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Internal ID 1baa13cd-c1ff-40f0-b488-278af691d066
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Aminosaccharides > Aminoglycosides
IUPAC Name 15-[(4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl)oxymethyl]-6-[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-16-ethyl-5,7,9-trimethyl-1-oxacyclohexadeca-3,11,13-triene-2,10-dione
SMILES (Canonical) CCC1C(C=CC=CC(=O)C(CC(C(C(C=CC(=O)O1)C)OC2C(C(CC(O2)C)N(C)C)O)C)C)COC3C(C(C(C(O3)C)O)O)OC
SMILES (Isomeric) CCC1C(C=CC=CC(=O)C(CC(C(C(C=CC(=O)O1)C)OC2C(C(CC(O2)C)N(C)C)O)C)C)COC3C(C(C(C(O3)C)O)O)OC
InChI InChI=1S/C36H59NO11/c1-10-28-25(19-44-36-34(43-9)32(42)30(40)24(6)46-36)13-11-12-14-27(38)21(3)17-22(4)33(20(2)15-16-29(39)47-28)48-35-31(41)26(37(7)8)18-23(5)45-35/h11-16,20-26,28,30-36,40-42H,10,17-19H2,1-9H3
InChI Key FPIDCOOKEJFXFI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C36H59NO11
Molecular Weight 681.90 g/mol
Exact Mass 681.40881170 g/mol
Topological Polar Surface Area (TPSA) 153.00 Ų
XlogP 3.60
Atomic LogP (AlogP) 2.78
H-Bond Acceptor 12
H-Bond Donor 3
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 15-[(4,5-Dihydroxy-3-methoxy-6-methyloxan-2-yl)oxymethyl]-6-[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-16-ethyl-5,7,9-trimethyl-1-oxacyclohexadeca-3,11,13-triene-2,10-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6172 61.72%
Caco-2 - 0.8489 84.89%
Blood Brain Barrier - 0.8750 87.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.5823 58.23%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8708 87.08%
OATP1B3 inhibitior + 0.8719 87.19%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.7621 76.21%
P-glycoprotein inhibitior + 0.7203 72.03%
P-glycoprotein substrate + 0.7100 71.00%
CYP3A4 substrate + 0.7037 70.37%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8800 88.00%
CYP3A4 inhibition - 0.5439 54.39%
CYP2C9 inhibition - 0.9067 90.67%
CYP2C19 inhibition - 0.8781 87.81%
CYP2D6 inhibition - 0.9084 90.84%
CYP1A2 inhibition - 0.9128 91.28%
CYP2C8 inhibition - 0.5592 55.92%
CYP inhibitory promiscuity - 0.9626 96.26%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5339 53.39%
Eye corrosion - 0.9878 98.78%
Eye irritation - 0.9281 92.81%
Skin irritation - 0.8008 80.08%
Skin corrosion - 0.9374 93.74%
Ames mutagenesis + 0.5046 50.46%
Human Ether-a-go-go-Related Gene inhibition + 0.6559 65.59%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.7073 70.73%
skin sensitisation - 0.8903 89.03%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.9138 91.38%
Acute Oral Toxicity (c) III 0.7341 73.41%
Estrogen receptor binding + 0.7044 70.44%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.5459 54.59%
Glucocorticoid receptor binding + 0.6323 63.23%
Aromatase binding - 0.4897 48.97%
PPAR gamma + 0.6593 65.93%
Honey bee toxicity - 0.6337 63.37%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.8742 87.42%

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 98.33% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.16% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.25% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.93% 89.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.72% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.57% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 87.90% 94.73%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.33% 96.77%
CHEMBL226 P30542 Adenosine A1 receptor 83.96% 95.93%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 83.43% 96.21%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.30% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.21% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.70% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 81.60% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.38% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.08% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.01% 99.17%

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 3056298
LOTUS LTS0240899
wikiData Q104999206