5-O-beta-D-mycaminosyl-20-oxotylonolide

Details

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Internal ID 8f352fd0-f84f-46a0-bca3-4e106b9b35bc
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Aminosaccharides > Aminoglycosides
IUPAC Name 2-[(4R,5S,6S,7R,9R,11E,13E,15S,16R)-6-[(2R,3R,4S,5S,6R)-4-(dimethylamino)-3,5-dihydroxy-6-methyloxan-2-yl]oxy-16-ethyl-4-hydroxy-5,9,13,15-tetramethyl-2,10-dioxo-1-oxacyclohexadeca-11,13-dien-7-yl]acetaldehyde
SMILES (Canonical) CCC1C(C=C(C=CC(=O)C(CC(C(C(C(CC(=O)O1)O)C)OC2C(C(C(C(O2)C)O)N(C)C)O)CC=O)C)C)C
SMILES (Isomeric) CC[C@@H]1[C@H](/C=C(/C=C/C(=O)[C@@H](C[C@@H]([C@@H]([C@H]([C@@H](CC(=O)O1)O)C)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)C)O)N(C)C)O)CC=O)C)\C)C
InChI InChI=1S/C31H51NO9/c1-9-25-19(4)14-17(2)10-11-23(34)18(3)15-22(12-13-33)30(20(5)24(35)16-26(36)40-25)41-31-29(38)27(32(7)8)28(37)21(6)39-31/h10-11,13-14,18-22,24-25,27-31,35,37-38H,9,12,15-16H2,1-8H3/b11-10+,17-14+/t18-,19+,20+,21-,22+,24-,25-,27+,28-,29-,30-,31+/m1/s1
InChI Key FERSDKADYZRIAA-CQGKBTLCSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C31H51NO9
Molecular Weight 581.70 g/mol
Exact Mass 581.35638220 g/mol
Topological Polar Surface Area (TPSA) 143.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.43
H-Bond Acceptor 10
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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CHEBI:77009
20-oxo-5-O-beta-mycaminosyltylactone
23-Deoxy-5-O-beta-mycaminosyltylonolide
(4R,5S,6S,7R,9R,11E,13E,15S,16R)-16-ethyl-4-hydroxy-5,9,13,15-tetramethyl-2,10-dioxo-7-(2-oxoethyl)-1-oxacyclohexadeca-11,13-dien-6-yl 3,6-dideoxy-3-(dimethylamino)-beta-D-glucopyranoside
20-oxo-5-O-beta-D-mycaminosyltylonolide
CHEMBL43197
CHEBI:134191
C20760
Q27146533
(4R,5S,6S,7R,9R,11E,13E,15S,16R)-16-ethyl-4-hydroxy-5,9,13,15-tetramethyl-2,10-dioxo-7-(2-oxoethyl)oxacyclohexadeca-11,13-dien-6-yl 3,6-dideoxy-3-(dimethylamino)-beta-D-glucopyranoside
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 5-O-beta-D-mycaminosyl-20-oxotylonolide

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 - 0.7944 79.44%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.9143 91.43%
Subcellular localzation Mitochondria 0.4994 49.94%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8530 85.30%
OATP1B3 inhibitior + 0.9428 94.28%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7506 75.06%
P-glycoprotein inhibitior + 0.6657 66.57%
P-glycoprotein substrate + 0.6964 69.64%
CYP3A4 substrate + 0.6777 67.77%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8495 84.95%
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 + 0.4832 48.32%
CYP inhibitory promiscuity - 0.9655 96.55%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5324 53.24%
Eye corrosion - 0.9829 98.29%
Eye irritation - 0.9390 93.90%
Skin irritation - 0.7618 76.18%
Skin corrosion - 0.9269 92.69%
Ames mutagenesis - 0.5354 53.54%
Human Ether-a-go-go-Related Gene inhibition - 0.3714 37.14%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.6928 69.28%
skin sensitisation - 0.8521 85.21%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.6789 67.89%
Acute Oral Toxicity (c) III 0.6731 67.31%
Estrogen receptor binding + 0.8243 82.43%
Androgen receptor binding + 0.6027 60.27%
Thyroid receptor binding - 0.5533 55.33%
Glucocorticoid receptor binding + 0.6562 65.62%
Aromatase binding + 0.5265 52.65%
PPAR gamma + 0.6780 67.80%
Honey bee toxicity - 0.6457 64.57%
Biodegradation - 0.7750 77.50%
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 95.25% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.15% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.71% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.21% 91.11%
CHEMBL3714130 P46095 G-protein coupled receptor 6 91.35% 97.36%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.61% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 89.36% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.89% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.73% 99.17%
CHEMBL5103 Q969S8 Histone deacetylase 10 87.42% 90.08%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.28% 89.34%
CHEMBL1937 Q92769 Histone deacetylase 2 84.11% 94.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.69% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.36% 97.09%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 82.13% 82.38%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.80% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.78% 97.25%

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 13042283
LOTUS LTS0034235
wikiData Q27146533