Lasianthionoside B

Details

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Internal ID 9704c36b-1ed4-481b-b549-4915bcd63c20
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name (E)-4-[(1R,4S,5S,6R)-1,5-dihydroxy-2,2,6-trimethyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexyl]but-3-en-2-one
SMILES (Canonical) CC1C(C(CC(C1(C=CC(=O)C)O)(C)C)OC2C(C(C(C(O2)CO)O)O)O)O
SMILES (Isomeric) C[C@@H]1[C@@H]([C@H](CC([C@]1(/C=C/C(=O)C)O)(C)C)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)O
InChI InChI=1S/C19H32O9/c1-9(21)5-6-19(26)10(2)13(22)11(7-18(19,3)4)27-17-16(25)15(24)14(23)12(8-20)28-17/h5-6,10-17,20,22-26H,7-8H2,1-4H3/b6-5+/t10-,11+,12-,13+,14-,15+,16-,17-,19-/m1/s1
InChI Key GCTRVWYCEKAVDX-IGFYDYTQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H32O9
Molecular Weight 404.50 g/mol
Exact Mass 404.20463259 g/mol
Topological Polar Surface Area (TPSA) 157.00 Ų
XlogP -1.30
Atomic LogP (AlogP) -1.53
H-Bond Acceptor 9
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 Lasianthionoside B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6463 64.63%
Caco-2 - 0.7487 74.87%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.8240 82.40%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8993 89.93%
OATP1B3 inhibitior + 0.9171 91.71%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9383 93.83%
P-glycoprotein inhibitior - 0.7666 76.66%
P-glycoprotein substrate - 0.8498 84.98%
CYP3A4 substrate + 0.6518 65.18%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8863 88.63%
CYP3A4 inhibition - 0.8157 81.57%
CYP2C9 inhibition - 0.7962 79.62%
CYP2C19 inhibition - 0.8870 88.70%
CYP2D6 inhibition - 0.9450 94.50%
CYP1A2 inhibition - 0.8335 83.35%
CYP2C8 inhibition - 0.8753 87.53%
CYP inhibitory promiscuity - 0.8345 83.45%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6501 65.01%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.9728 97.28%
Skin irritation - 0.8355 83.55%
Skin corrosion - 0.9594 95.94%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6986 69.86%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.7906 79.06%
skin sensitisation - 0.8207 82.07%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.7079 70.79%
Acute Oral Toxicity (c) III 0.7344 73.44%
Estrogen receptor binding + 0.6064 60.64%
Androgen receptor binding - 0.5052 50.52%
Thyroid receptor binding + 0.6943 69.43%
Glucocorticoid receptor binding + 0.5805 58.05%
Aromatase binding + 0.6614 66.14%
PPAR gamma - 0.5283 52.83%
Honey bee toxicity - 0.7001 70.01%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7555 75.55%
Fish aquatic toxicity + 0.7661 76.61%

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 97.49% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.27% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.29% 97.25%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 90.45% 91.24%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.81% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.21% 96.95%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.55% 91.07%
CHEMBL340 P08684 Cytochrome P450 3A4 82.78% 91.19%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.48% 89.00%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 82.31% 97.34%
CHEMBL5255 O00206 Toll-like receptor 4 82.21% 92.50%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.76% 85.14%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.00% 95.50%

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.
Lasianthus fordii
Taxus baccata
Taxus canadensis
Taxus cuspidata
Taxus mairei

Cross-Links

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PubChem 101338642
LOTUS LTS0126573
wikiData Q105100430