2-[3-methoxy-3-oxo-1-[[(1S,2R,7S,10R,11S,14R,15R,16R,19S)-10,14,16-trimethyl-17,20,21-trioxahexacyclo[14.4.1.01,14.02,11.05,10.015,19]henicos-4-en-7-yl]oxy]propoxy]propanoic acid

Details

Top
Internal ID c3d0c0b9-b66c-4f9e-8d95-7c8978cfce32
Taxonomy Organoheterocyclic compounds > Naphthofurans
IUPAC Name 2-[3-methoxy-3-oxo-1-[[(1S,2R,7S,10R,11S,14R,15R,16R,19S)-10,14,16-trimethyl-17,20,21-trioxahexacyclo[14.4.1.01,14.02,11.05,10.015,19]henicos-4-en-7-yl]oxy]propoxy]propanoic acid
SMILES (Canonical) CC(C(=O)O)OC(CC(=O)OC)OC1CCC2(C3CCC4(C5C6COC5(OC4(C3CC=C2C1)O6)C)C)C
SMILES (Isomeric) CC(C(=O)O)OC(CC(=O)OC)O[C@H]1CC[C@@]2([C@H]3CC[C@@]4([C@@H]5[C@H]6CO[C@@]5(O[C@]4([C@@H]3CC=C2C1)O6)C)C)C
InChI InChI=1S/C28H40O9/c1-15(24(30)31)34-22(13-21(29)32-5)35-17-8-10-25(2)16(12-17)6-7-19-18(25)9-11-26(3)23-20-14-33-27(23,4)37-28(19,26)36-20/h6,15,17-20,22-23H,7-14H2,1-5H3,(H,30,31)/t15?,17-,18-,19+,20+,22?,23-,25-,26+,27+,28-/m0/s1
InChI Key LAGKFZXTTOABAX-RAAGZJLXSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C28H40O9
Molecular Weight 520.60 g/mol
Exact Mass 520.26723285 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.79
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-[3-methoxy-3-oxo-1-[[(1S,2R,7S,10R,11S,14R,15R,16R,19S)-10,14,16-trimethyl-17,20,21-trioxahexacyclo[14.4.1.01,14.02,11.05,10.015,19]henicos-4-en-7-yl]oxy]propoxy]propanoic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9803 98.03%
Caco-2 - 0.7255 72.55%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8298 82.98%
OATP2B1 inhibitior - 0.7158 71.58%
OATP1B1 inhibitior + 0.8443 84.43%
OATP1B3 inhibitior + 0.9349 93.49%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5271 52.71%
BSEP inhibitior + 0.6474 64.74%
P-glycoprotein inhibitior + 0.7258 72.58%
P-glycoprotein substrate + 0.6242 62.42%
CYP3A4 substrate + 0.7034 70.34%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8796 87.96%
CYP3A4 inhibition - 0.9172 91.72%
CYP2C9 inhibition - 0.8715 87.15%
CYP2C19 inhibition - 0.9397 93.97%
CYP2D6 inhibition - 0.9393 93.93%
CYP1A2 inhibition - 0.8797 87.97%
CYP2C8 inhibition + 0.7453 74.53%
CYP inhibitory promiscuity - 0.9291 92.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5274 52.74%
Eye corrosion - 0.9877 98.77%
Eye irritation - 0.9395 93.95%
Skin irritation - 0.6003 60.03%
Skin corrosion - 0.9392 93.92%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3674 36.74%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.6266 62.66%
skin sensitisation - 0.8900 89.00%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.5967 59.67%
Acute Oral Toxicity (c) I 0.4432 44.32%
Estrogen receptor binding + 0.6556 65.56%
Androgen receptor binding + 0.7567 75.67%
Thyroid receptor binding + 0.5765 57.65%
Glucocorticoid receptor binding + 0.7282 72.82%
Aromatase binding + 0.6797 67.97%
PPAR gamma + 0.5610 56.10%
Honey bee toxicity - 0.7630 76.30%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6134 61.34%
Fish aquatic toxicity + 0.9579 95.79%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.29% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.76% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.84% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.56% 85.14%
CHEMBL3359 P21462 Formyl peptide receptor 1 91.76% 93.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.06% 97.25%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 88.17% 95.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.99% 99.17%
CHEMBL2581 P07339 Cathepsin D 86.72% 98.95%
CHEMBL5028 O14672 ADAM10 85.80% 97.50%
CHEMBL4227 P25090 Lipoxin A4 receptor 85.72% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.12% 95.89%
CHEMBL2996 Q05655 Protein kinase C delta 85.02% 97.79%
CHEMBL4072 P07858 Cathepsin B 84.53% 93.67%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.08% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.81% 100.00%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 81.29% 91.03%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.78% 92.62%

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.
There are no matching plants.

Cross-Links

Top
PubChem 162982521
LOTUS LTS0178022
wikiData Q105148634