methyl (2S)-2-[(1S,2R,5R,6R,10R,11S,13S,16S)-6-(furan-3-yl)-11-hydroxy-1,5,15,15-tetramethyl-8,14,17-trioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadecan-16-yl]-2-hydroxyacetate

Details

Top
Internal ID b795e2b7-50aa-4487-b603-61bf1941a5ea
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids > Limonoids
IUPAC Name methyl (2S)-2-[(1S,2R,5R,6R,10R,11S,13S,16S)-6-(furan-3-yl)-11-hydroxy-1,5,15,15-tetramethyl-8,14,17-trioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadecan-16-yl]-2-hydroxyacetate
SMILES (Canonical) CC1(C(C2(C3CCC4(C(C3(CC(C1=O)C2=O)O)CC(=O)OC4C5=COC=C5)C)C)C(C(=O)OC)O)C
SMILES (Isomeric) C[C@@]12CC[C@@H]3[C@@]4([C@H](C(C(=O)[C@@H](C4=O)C[C@@]3([C@@H]1CC(=O)O[C@H]2C5=COC=C5)O)(C)C)[C@@H](C(=O)OC)O)C
InChI InChI=1S/C27H34O9/c1-24(2)19(18(29)23(32)34-5)26(4)15-6-8-25(3)16(27(15,33)11-14(20(24)30)21(26)31)10-17(28)36-22(25)13-7-9-35-12-13/h7,9,12,14-16,18-19,22,29,33H,6,8,10-11H2,1-5H3/t14-,15+,16+,18-,19-,22-,25+,26+,27+/m0/s1
InChI Key GKXWKJLURBIZRZ-HTQKDQDZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C27H34O9
Molecular Weight 502.60 g/mol
Exact Mass 502.22028266 g/mol
Topological Polar Surface Area (TPSA) 140.00 Ų
XlogP 1.70
Atomic LogP (AlogP) 2.39
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of methyl (2S)-2-[(1S,2R,5R,6R,10R,11S,13S,16S)-6-(furan-3-yl)-11-hydroxy-1,5,15,15-tetramethyl-8,14,17-trioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadecan-16-yl]-2-hydroxyacetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9648 96.48%
Caco-2 - 0.7501 75.01%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.8104 81.04%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior - 0.3807 38.07%
OATP1B3 inhibitior - 0.2233 22.33%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8321 83.21%
BSEP inhibitior + 0.6528 65.28%
P-glycoprotein inhibitior + 0.6282 62.82%
P-glycoprotein substrate + 0.5248 52.48%
CYP3A4 substrate + 0.7128 71.28%
CYP2C9 substrate - 0.8002 80.02%
CYP2D6 substrate - 0.8392 83.92%
CYP3A4 inhibition + 0.5526 55.26%
CYP2C9 inhibition - 0.8366 83.66%
CYP2C19 inhibition - 0.8759 87.59%
CYP2D6 inhibition - 0.9408 94.08%
CYP1A2 inhibition - 0.8488 84.88%
CYP2C8 inhibition + 0.6439 64.39%
CYP inhibitory promiscuity - 0.9549 95.49%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4981 49.81%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.9229 92.29%
Skin irritation - 0.6703 67.03%
Skin corrosion - 0.9117 91.17%
Ames mutagenesis - 0.7070 70.70%
Human Ether-a-go-go-Related Gene inhibition - 0.3679 36.79%
Micronuclear - 0.7500 75.00%
Hepatotoxicity - 0.5623 56.23%
skin sensitisation - 0.9035 90.35%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.7462 74.62%
Acute Oral Toxicity (c) I 0.6329 63.29%
Estrogen receptor binding + 0.8217 82.17%
Androgen receptor binding + 0.7363 73.63%
Thyroid receptor binding + 0.5703 57.03%
Glucocorticoid receptor binding + 0.8693 86.93%
Aromatase binding + 0.7193 71.93%
PPAR gamma + 0.6708 67.08%
Honey bee toxicity - 0.7867 78.67%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9748 97.48%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.06% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.90% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.98% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.49% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.34% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 92.24% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.68% 97.25%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.20% 97.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.92% 89.00%
CHEMBL2581 P07339 Cathepsin D 85.71% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.40% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.05% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.32% 92.62%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.66% 100.00%
CHEMBL5028 O14672 ADAM10 80.76% 97.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.62% 86.33%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 80.57% 91.24%
CHEMBL340 P08684 Cytochrome P450 3A4 80.12% 91.19%

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.
Khaya senegalensis

Cross-Links

Top
PubChem 10940063
LOTUS LTS0025346
wikiData Q105010454