12-Epi-2-O-deacetyltrichilin B

Details

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Internal ID d4576ead-e6fc-4da3-a5f9-f18565434b4e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids > Limonoids
IUPAC Name [(1S,2R,4S,5R,6S,8R,10S,11S,12R,14R,15S,19R,20R,21S)-21-acetyloxy-6-(furan-3-yl)-4,12,19,20-tetrahydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.01,14.02,11.05,10.08,10]henicosan-16-yl] 2-methylbutanoate
SMILES (Canonical) CCC(C)C(=O)OC1C2(C3CC(C4(C(C3(CO1)C(C(C2OC(=O)C)O)O)C(=O)C(C5(C46C(O6)CC5C7=COC=C7)C)O)C)O)C
SMILES (Isomeric) CCC(C)C(=O)OC1[C@]2([C@@H]3C[C@H]([C@@]4([C@@H]([C@@]3(CO1)[C@H]([C@H]([C@H]2OC(=O)C)O)O)C(=O)[C@H]([C@@]5([C@]46[C@H](O6)C[C@H]5C7=COC=C7)C)O)C)O)C
InChI InChI=1S/C33H44O12/c1-7-14(2)27(40)44-28-29(4)18-11-19(35)31(6)23(32(18,13-42-28)25(39)22(37)26(29)43-15(3)34)21(36)24(38)30(5)17(16-8-9-41-12-16)10-20-33(30,31)45-20/h8-9,12,14,17-20,22-26,28,35,37-39H,7,10-11,13H2,1-6H3/t14?,17-,18-,19+,20+,22+,23-,24+,25-,26+,28?,29-,30+,31+,32-,33+/m0/s1
InChI Key UILDHUYKTXNKSK-WAGXAHHKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C33H44O12
Molecular Weight 632.70 g/mol
Exact Mass 632.28327683 g/mol
Topological Polar Surface Area (TPSA) 186.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.46
H-Bond Acceptor 12
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 12-Epi-2-O-deacetyltrichilin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9424 94.24%
Caco-2 - 0.8221 82.21%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7233 72.33%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7105 71.05%
OATP1B3 inhibitior + 0.8337 83.37%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8632 86.32%
P-glycoprotein inhibitior + 0.7120 71.20%
P-glycoprotein substrate + 0.6826 68.26%
CYP3A4 substrate + 0.7057 70.57%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8370 83.70%
CYP3A4 inhibition + 0.6312 63.12%
CYP2C9 inhibition - 0.7958 79.58%
CYP2C19 inhibition - 0.8353 83.53%
CYP2D6 inhibition - 0.9459 94.59%
CYP1A2 inhibition - 0.8526 85.26%
CYP2C8 inhibition + 0.6939 69.39%
CYP inhibitory promiscuity - 0.8706 87.06%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5520 55.20%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.9144 91.44%
Skin irritation - 0.7056 70.56%
Skin corrosion - 0.9364 93.64%
Ames mutagenesis - 0.5201 52.01%
Human Ether-a-go-go-Related Gene inhibition + 0.7279 72.79%
Micronuclear - 0.5600 56.00%
Hepatotoxicity + 0.6126 61.26%
skin sensitisation - 0.8861 88.61%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.5411 54.11%
Acute Oral Toxicity (c) III 0.3936 39.36%
Estrogen receptor binding + 0.7894 78.94%
Androgen receptor binding + 0.7516 75.16%
Thyroid receptor binding + 0.5488 54.88%
Glucocorticoid receptor binding + 0.7580 75.80%
Aromatase binding + 0.6965 69.65%
PPAR gamma + 0.7508 75.08%
Honey bee toxicity - 0.7051 70.51%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9842 98.42%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.36% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.25% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.16% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.13% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.97% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 96.51% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.64% 97.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 90.50% 96.77%
CHEMBL3922 P50579 Methionine aminopeptidase 2 89.02% 97.28%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.92% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.60% 95.56%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 87.16% 98.75%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 86.44% 95.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.33% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.72% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 84.22% 94.73%
CHEMBL2996 Q05655 Protein kinase C delta 84.21% 97.79%
CHEMBL340 P08684 Cytochrome P450 3A4 84.04% 91.19%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.75% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.17% 94.00%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 82.09% 91.24%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.05% 92.62%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.31% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.60% 100.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.37% 93.00%

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.
Melia azedarach

Cross-Links

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PubChem 102156448
NPASS NPC200793