5-O-mycaminosyl tylactone

Details

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Internal ID 77cb1554-6a30-4677-92d2-e6dddc159da5
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Aminosaccharides > Aminoglycosides
IUPAC Name (11E,13E)-6-[4-(dimethylamino)-3,5-dihydroxy-6-methyloxan-2-yl]oxy-7,16-diethyl-4-hydroxy-5,9,13,15-tetramethyl-1-oxacyclohexadeca-11,13-diene-2,10-dione
SMILES (Canonical) CCC1CC(C(=O)C=CC(=CC(C(OC(=O)CC(C(C1OC2C(C(C(C(O2)C)O)N(C)C)O)C)O)CC)C)C)C
SMILES (Isomeric) CCC1CC(C(=O)/C=C/C(=C/C(C(OC(=O)CC(C(C1OC2C(C(C(C(O2)C)O)N(C)C)O)C)O)CC)C)/C)C
InChI InChI=1S/C31H53NO8/c1-10-22-15-18(4)23(33)13-12-17(3)14-19(5)25(11-2)39-26(35)16-24(34)20(6)30(22)40-31-29(37)27(32(8)9)28(36)21(7)38-31/h12-14,18-22,24-25,27-31,34,36-37H,10-11,15-16H2,1-9H3/b13-12+,17-14+
InChI Key BMKVJAXXBOWJEE-MIFVOYFBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H53NO8
Molecular Weight 567.80 g/mol
Exact Mass 567.37711765 g/mol
Topological Polar Surface Area (TPSA) 126.00 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.25
H-Bond Acceptor 9
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-O-mycaminosyl tylactone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6509 65.09%
Caco-2 - 0.7719 77.19%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.8571 85.71%
Subcellular localzation Mitochondria 0.4994 49.94%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8539 85.39%
OATP1B3 inhibitior + 0.9428 94.28%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8275 82.75%
P-glycoprotein inhibitior + 0.6410 64.10%
P-glycoprotein substrate + 0.6478 64.78%
CYP3A4 substrate + 0.6747 67.47%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8480 84.80%
CYP3A4 inhibition - 0.8160 81.60%
CYP2C9 inhibition - 0.8926 89.26%
CYP2C19 inhibition - 0.8134 81.34%
CYP2D6 inhibition - 0.8920 89.20%
CYP1A2 inhibition - 0.8448 84.48%
CYP2C8 inhibition - 0.6291 62.91%
CYP inhibitory promiscuity - 0.9655 96.55%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5324 53.24%
Eye corrosion - 0.9829 98.29%
Eye irritation - 0.9331 93.31%
Skin irritation - 0.7618 76.18%
Skin corrosion - 0.9269 92.69%
Ames mutagenesis - 0.5454 54.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4647 46.47%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.6553 65.53%
skin sensitisation - 0.8521 85.21%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.7056 70.56%
Acute Oral Toxicity (c) III 0.6731 67.31%
Estrogen receptor binding + 0.7931 79.31%
Androgen receptor binding + 0.5770 57.70%
Thyroid receptor binding - 0.5459 54.59%
Glucocorticoid receptor binding + 0.6270 62.70%
Aromatase binding + 0.5576 55.76%
PPAR gamma + 0.6221 62.21%
Honey bee toxicity - 0.6642 66.42%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.7164 71.64%

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 95.62% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.54% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.38% 91.11%
CHEMBL3714130 P46095 G-protein coupled receptor 6 93.07% 97.36%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.62% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.06% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 87.15% 94.73%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.46% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.39% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.34% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.23% 95.89%
CHEMBL5103 Q969S8 Histone deacetylase 10 84.26% 90.08%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 83.67% 95.64%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.25% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Blainvillea acmella
Seriphidium fragrans
Seriphidium gypsaceum

Cross-Links

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PubChem 13255248
LOTUS LTS0196540
wikiData Q104907821