[(5R,7R,8R,9R,10S,11S,12R,13S,17R)-7-acetyloxy-12-hydroxy-17-(2-hydroxy-5-oxo-2H-furan-4-yl)-4,4,8,10,13-pentamethyl-3-oxo-5,6,7,9,11,12,16,17-octahydrocyclopenta[a]phenanthren-11-yl] 2-hydroxy-2-methylpropanoate

Details

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Internal ID 7d3b4cdb-8497-4e80-8d52-6d11efe3aa1b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids > Limonoids
IUPAC Name [(5R,7R,8R,9R,10S,11S,12R,13S,17R)-7-acetyloxy-12-hydroxy-17-(2-hydroxy-5-oxo-2H-furan-4-yl)-4,4,8,10,13-pentamethyl-3-oxo-5,6,7,9,11,12,16,17-octahydrocyclopenta[a]phenanthren-11-yl] 2-hydroxy-2-methylpropanoate
SMILES (Canonical) CC(=O)OC1CC2C(C(=O)C=CC2(C3C1(C4=CCC(C4(C(C3OC(=O)C(C)(C)O)O)C)C5=CC(OC5=O)O)C)C)(C)C
SMILES (Isomeric) CC(=O)O[C@@H]1C[C@@H]2[C@](C=CC(=O)C2(C)C)([C@@H]3[C@@]1(C4=CC[C@H]([C@@]4([C@H]([C@H]3OC(=O)C(C)(C)O)O)C)C5=CC(OC5=O)O)C)C
InChI InChI=1S/C32H42O10/c1-15(33)40-21-14-19-28(2,3)20(34)11-12-30(19,6)24-23(42-27(38)29(4,5)39)25(36)31(7)17(9-10-18(31)32(21,24)8)16-13-22(35)41-26(16)37/h10-13,17,19,21-25,35-36,39H,9,14H2,1-8H3/t17-,19-,21+,22?,23-,24+,25-,30-,31-,32+/m0/s1
InChI Key BQVRARANLWBOLS-IXTPREFVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C32H42O10
Molecular Weight 586.70 g/mol
Exact Mass 586.27779753 g/mol
Topological Polar Surface Area (TPSA) 157.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.54
H-Bond Acceptor 10
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(5R,7R,8R,9R,10S,11S,12R,13S,17R)-7-acetyloxy-12-hydroxy-17-(2-hydroxy-5-oxo-2H-furan-4-yl)-4,4,8,10,13-pentamethyl-3-oxo-5,6,7,9,11,12,16,17-octahydrocyclopenta[a]phenanthren-11-yl] 2-hydroxy-2-methylpropanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9875 98.75%
Caco-2 - 0.7832 78.32%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7798 77.98%
OATP2B1 inhibitior - 0.7173 71.73%
OATP1B1 inhibitior + 0.7869 78.69%
OATP1B3 inhibitior + 0.8282 82.82%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8768 87.68%
P-glycoprotein inhibitior + 0.7368 73.68%
P-glycoprotein substrate + 0.5488 54.88%
CYP3A4 substrate + 0.7282 72.82%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8992 89.92%
CYP3A4 inhibition - 0.7213 72.13%
CYP2C9 inhibition - 0.7188 71.88%
CYP2C19 inhibition - 0.8299 82.99%
CYP2D6 inhibition - 0.9185 91.85%
CYP1A2 inhibition - 0.7804 78.04%
CYP2C8 inhibition + 0.5958 59.58%
CYP inhibitory promiscuity - 0.5741 57.41%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Danger 0.4903 49.03%
Eye corrosion - 0.9870 98.70%
Eye irritation - 0.9188 91.88%
Skin irritation - 0.5785 57.85%
Skin corrosion - 0.9071 90.71%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.5499 54.99%
skin sensitisation - 0.7689 76.89%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.5927 59.27%
Acute Oral Toxicity (c) III 0.4124 41.24%
Estrogen receptor binding + 0.7407 74.07%
Androgen receptor binding + 0.6896 68.96%
Thyroid receptor binding + 0.5971 59.71%
Glucocorticoid receptor binding + 0.7138 71.38%
Aromatase binding + 0.6814 68.14%
PPAR gamma + 0.7233 72.33%
Honey bee toxicity - 0.6464 64.64%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9827 98.27%

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 98.55% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.67% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.65% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.45% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.41% 97.25%
CHEMBL2581 P07339 Cathepsin D 89.64% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.89% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.01% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.87% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.00% 95.56%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.34% 91.07%
CHEMBL5028 O14672 ADAM10 84.31% 97.50%
CHEMBL2996 Q05655 Protein kinase C delta 84.23% 97.79%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.05% 99.23%
CHEMBL340 P08684 Cytochrome P450 3A4 82.14% 91.19%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.64% 99.17%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.44% 97.14%
CHEMBL3401 O75469 Pregnane X receptor 80.34% 94.73%

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.
Azadirachta indica

Cross-Links

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PubChem 13875774
LOTUS LTS0136045
wikiData Q104944590