[8-Hydroxy-5-(3-hydroxy-3-methylbutanoyl)oxy-10-methyl-11-oxo-4,12-dioxapentacyclo[7.7.0.01,6.02,13.010,15]hexadec-2-en-14-yl] 2,3-dimethyloxirane-2-carboxylate

Details

Top
Internal ID 5eef174c-c998-4411-be50-b09893972b26
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name [8-hydroxy-5-(3-hydroxy-3-methylbutanoyl)oxy-10-methyl-11-oxo-4,12-dioxapentacyclo[7.7.0.01,6.02,13.010,15]hexadec-2-en-14-yl] 2,3-dimethyloxirane-2-carboxylate
SMILES (Canonical) CC1C(O1)(C)C(=O)OC2C3CC45C6CC(C4C3(C(=O)OC2C5=COC6OC(=O)CC(C)(C)O)C)O
SMILES (Isomeric) CC1C(O1)(C)C(=O)OC2C3CC45C6CC(C4C3(C(=O)OC2C5=COC6OC(=O)CC(C)(C)O)C)O
InChI InChI=1S/C25H32O10/c1-10-24(5,35-10)21(29)34-16-12-7-25-11-6-14(26)18(25)23(12,4)20(28)33-17(16)13(25)9-31-19(11)32-15(27)8-22(2,3)30/h9-12,14,16-19,26,30H,6-8H2,1-5H3
InChI Key MTSOBXIXNFODRC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C25H32O10
Molecular Weight 492.50 g/mol
Exact Mass 492.19954721 g/mol
Topological Polar Surface Area (TPSA) 141.00 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.97
H-Bond Acceptor 10
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of [8-Hydroxy-5-(3-hydroxy-3-methylbutanoyl)oxy-10-methyl-11-oxo-4,12-dioxapentacyclo[7.7.0.01,6.02,13.010,15]hexadec-2-en-14-yl] 2,3-dimethyloxirane-2-carboxylate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9689 96.89%
Caco-2 - 0.7987 79.87%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7176 71.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8044 80.44%
OATP1B3 inhibitior + 0.9116 91.16%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5715 57.15%
P-glycoprotein inhibitior + 0.6251 62.51%
P-glycoprotein substrate + 0.6384 63.84%
CYP3A4 substrate + 0.7072 70.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8589 85.89%
CYP3A4 inhibition - 0.5809 58.09%
CYP2C9 inhibition - 0.8391 83.91%
CYP2C19 inhibition - 0.8868 88.68%
CYP2D6 inhibition - 0.9406 94.06%
CYP1A2 inhibition - 0.8685 86.85%
CYP2C8 inhibition - 0.5629 56.29%
CYP inhibitory promiscuity - 0.9006 90.06%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5285 52.85%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.9301 93.01%
Skin irritation - 0.5161 51.61%
Skin corrosion - 0.9277 92.77%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3646 36.46%
Micronuclear - 0.5300 53.00%
Hepatotoxicity + 0.6372 63.72%
skin sensitisation - 0.7943 79.43%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.6765 67.65%
Acute Oral Toxicity (c) I 0.7147 71.47%
Estrogen receptor binding + 0.7382 73.82%
Androgen receptor binding + 0.6918 69.18%
Thyroid receptor binding + 0.5185 51.85%
Glucocorticoid receptor binding + 0.6891 68.91%
Aromatase binding + 0.6544 65.44%
PPAR gamma + 0.6024 60.24%
Honey bee toxicity - 0.7775 77.75%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9906 99.06%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.91% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.01% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.80% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.26% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.96% 97.09%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 91.84% 91.07%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 91.56% 97.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.74% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.71% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 89.65% 83.82%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.12% 86.33%
CHEMBL2996 Q05655 Protein kinase C delta 86.30% 97.79%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.94% 99.23%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.54% 82.69%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.44% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 83.62% 94.73%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 82.66% 97.33%
CHEMBL299 P17252 Protein kinase C alpha 82.37% 98.03%
CHEMBL5028 O14672 ADAM10 80.97% 97.50%

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.
Salvia apiana
Trixis grisebachii

Cross-Links

Top
PubChem 14355445
LOTUS LTS0198829
wikiData Q105302942