Hosenkoside D

Details

Top
Internal ID 8e13ac87-d92f-4b38-b67b-a976f14c14fd
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (2R,3R,4S,5S,6R)-2-[[(1R,2S,2'S,4aR,4bR,6aS,7R,8S,10aR,10bR,12aR)-7-hydroxy-2'-[(2S)-1-hydroxypropan-2-yl]-1,4a,10a,10b-tetramethyl-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[3,4,4b,5,6,6a,7,9,10,11,12,12a-dodecahydro-2H-chrysene-8,5'-oxane]-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H72O15/c1-21(16-43)23-8-13-42(20-53-23)15-14-40(4)22(35(42)52)6-7-27-38(2)11-10-28(57-37-34(51)32(49)30(47)25(18-45)56-37)39(3,26(38)9-12-41(27,40)5)19-54-36-33(50)31(48)29(46)24(17-44)55-36/h21-37,43-52H,6-20H2,1-5H3/t21-,22+,23-,24+,25+,26+,27+,28-,29+,30+,31-,32-,33+,34+,35+,36+,37-,38-,39-,40+,41+,42+/m0/s1
InChI Key AKYWEEHCEBAGNO-FWNFINTESA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C42H72O15
Molecular Weight 817.00 g/mol
Exact Mass 816.48712159 g/mol
Topological Polar Surface Area (TPSA) 248.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 0.19
H-Bond Acceptor 15
H-Bond Donor 10
Rotatable Bonds 9

Synonyms

Top
156823-94-8
orb1942582
HY-N12050
CS-0891165
H50738

2D Structure

Top
2D Structure of Hosenkoside D

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7127 71.27%
Caco-2 - 0.8771 87.71%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.6987 69.87%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8572 85.72%
OATP1B3 inhibitior + 0.8695 86.95%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.7989 79.89%
P-glycoprotein inhibitior + 0.7366 73.66%
P-glycoprotein substrate - 0.6233 62.33%
CYP3A4 substrate + 0.7232 72.32%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8237 82.37%
CYP3A4 inhibition - 0.9673 96.73%
CYP2C9 inhibition - 0.9196 91.96%
CYP2C19 inhibition - 0.8854 88.54%
CYP2D6 inhibition - 0.9670 96.70%
CYP1A2 inhibition - 0.8866 88.66%
CYP2C8 inhibition + 0.6460 64.60%
CYP inhibitory promiscuity - 0.9670 96.70%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6899 68.99%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9065 90.65%
Skin irritation - 0.7625 76.25%
Skin corrosion - 0.9624 96.24%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6644 66.44%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.8072 80.72%
skin sensitisation - 0.9475 94.75%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.5523 55.23%
Acute Oral Toxicity (c) I 0.3844 38.44%
Estrogen receptor binding + 0.6966 69.66%
Androgen receptor binding + 0.7363 73.63%
Thyroid receptor binding - 0.5844 58.44%
Glucocorticoid receptor binding - 0.4773 47.73%
Aromatase binding + 0.6268 62.68%
PPAR gamma + 0.6881 68.81%
Honey bee toxicity - 0.6934 69.34%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5750 57.50%
Fish aquatic toxicity + 0.7686 76.86%

Targets

Top

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.81% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.67% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.61% 97.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 91.45% 96.61%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.51% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.67% 91.11%
CHEMBL2243 O00519 Anandamide amidohydrolase 87.89% 97.53%
CHEMBL226 P30542 Adenosine A1 receptor 87.88% 95.93%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 87.54% 95.71%
CHEMBL1937 Q92769 Histone deacetylase 2 87.48% 94.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.77% 92.62%
CHEMBL2581 P07339 Cathepsin D 85.77% 98.95%
CHEMBL220 P22303 Acetylcholinesterase 85.39% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.76% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.59% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.24% 97.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.86% 89.00%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 81.26% 100.00%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 81.00% 89.05%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.90% 95.56%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.56% 100.00%
CHEMBL5028 O14672 ADAM10 80.34% 97.50%
CHEMBL3714130 P46095 G-protein coupled receptor 6 80.27% 97.36%

Plants that contains it

Top
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.
Impatiens balsamina

Cross-Links

Top
PubChem 163005572
LOTUS LTS0274397
wikiData Q104913935