Dendromoniliside B

Details

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Internal ID 46b11e3f-fe07-4288-b93b-1bb5325038ea
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name (1S,2R,5S,6S,7R,8S,11R)-11-(2-hydroxypropan-2-yl)-6-methyl-10-oxo-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9-oxatricyclo[6.2.1.02,6]undecane-5-carboxylic acid
SMILES (Canonical) CC12C(CCC1C(=O)O)C3C(C(C2OC4C(C(C(C(O4)CO)O)O)O)OC3=O)C(C)(C)O
SMILES (Isomeric) C[C@]12[C@H](CC[C@@H]1C(=O)O)[C@H]3[C@H]([C@@H]([C@@H]2O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)OC3=O)C(C)(C)O
InChI InChI=1S/C21H32O11/c1-20(2,29)11-10-7-4-5-8(17(26)27)21(7,3)16(15(11)31-18(10)28)32-19-14(25)13(24)12(23)9(6-22)30-19/h7-16,19,22-25,29H,4-6H2,1-3H3,(H,26,27)/t7-,8-,9-,10+,11-,12-,13+,14-,15+,16+,19+,21+/m1/s1
InChI Key VGJYMRIOASNQIL-DFKMWCPOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H32O11
Molecular Weight 460.50 g/mol
Exact Mass 460.19446183 g/mol
Topological Polar Surface Area (TPSA) 183.00 Ų
XlogP -1.20
Atomic LogP (AlogP) -1.77
H-Bond Acceptor 10
H-Bond Donor 6
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Dendromoniliside B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4877 48.77%
Caco-2 - 0.8589 85.89%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7701 77.01%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8755 87.55%
OATP1B3 inhibitior + 0.9295 92.95%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7171 71.71%
P-glycoprotein inhibitior - 0.6685 66.85%
P-glycoprotein substrate - 0.7351 73.51%
CYP3A4 substrate + 0.6704 67.04%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8915 89.15%
CYP3A4 inhibition - 0.9167 91.67%
CYP2C9 inhibition - 0.8288 82.88%
CYP2C19 inhibition - 0.8941 89.41%
CYP2D6 inhibition - 0.9526 95.26%
CYP1A2 inhibition - 0.8997 89.97%
CYP2C8 inhibition - 0.6011 60.11%
CYP inhibitory promiscuity - 0.9285 92.85%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6522 65.22%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.9533 95.33%
Skin irritation - 0.7230 72.30%
Skin corrosion - 0.9031 90.31%
Ames mutagenesis - 0.6754 67.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5249 52.49%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.9074 90.74%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.4660 46.60%
Acute Oral Toxicity (c) III 0.5672 56.72%
Estrogen receptor binding + 0.7015 70.15%
Androgen receptor binding + 0.6058 60.58%
Thyroid receptor binding - 0.5693 56.93%
Glucocorticoid receptor binding + 0.5462 54.62%
Aromatase binding - 0.4899 48.99%
PPAR gamma + 0.6433 64.33%
Honey bee toxicity - 0.8142 81.42%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.6685 66.85%

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 97.42% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.53% 97.25%
CHEMBL220 P22303 Acetylcholinesterase 95.12% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.54% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.88% 97.09%
CHEMBL2581 P07339 Cathepsin D 88.09% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.96% 86.33%
CHEMBL5255 O00206 Toll-like receptor 4 86.87% 92.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.29% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.91% 95.89%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.50% 96.61%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.08% 93.04%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.13% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.32% 97.14%
CHEMBL237 P41145 Kappa opioid receptor 82.58% 98.10%
CHEMBL3714130 P46095 G-protein coupled receptor 6 82.02% 97.36%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.71% 95.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.58% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.35% 94.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.35% 100.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 80.07% 96.21%

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.
Dendrobium moniliforme
Dendrobium nobile

Cross-Links

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PubChem 11005030
NPASS NPC197754
LOTUS LTS0157827
wikiData Q105285842