3-[(2R,3R)-2-(furan-3-yl)-4-[2-[(4R,5R)-4-(2-methoxy-2-oxoethyl)-3,3,5-trimethyl-6-oxocyclohexen-1-yl]acetyl]-3-methyl-6-oxo-2H-pyran-3-yl]propanoic acid

Details

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Internal ID 829a7eee-7e4e-40c8-a21f-a531060ee719
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name 3-[(2R,3R)-2-(furan-3-yl)-4-[2-[(4R,5R)-4-(2-methoxy-2-oxoethyl)-3,3,5-trimethyl-6-oxocyclohexen-1-yl]acetyl]-3-methyl-6-oxo-2H-pyran-3-yl]propanoic acid
SMILES (Canonical) CC1C(C(C=C(C1=O)CC(=O)C2=CC(=O)OC(C2(C)CCC(=O)O)C3=COC=C3)(C)C)CC(=O)OC
SMILES (Isomeric) C[C@@H]1[C@H](C(C=C(C1=O)CC(=O)C2=CC(=O)O[C@H]([C@]2(C)CCC(=O)O)C3=COC=C3)(C)C)CC(=O)OC
InChI InChI=1S/C27H32O9/c1-15-18(11-22(31)34-5)26(2,3)13-17(24(15)33)10-20(28)19-12-23(32)36-25(16-7-9-35-14-16)27(19,4)8-6-21(29)30/h7,9,12-15,18,25H,6,8,10-11H2,1-5H3,(H,29,30)/t15-,18-,25+,27-/m1/s1
InChI Key IYEWDOOFXNMWEJ-BDXWEOCWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H32O9
Molecular Weight 500.50 g/mol
Exact Mass 500.20463259 g/mol
Topological Polar Surface Area (TPSA) 137.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.98
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-[(2R,3R)-2-(furan-3-yl)-4-[2-[(4R,5R)-4-(2-methoxy-2-oxoethyl)-3,3,5-trimethyl-6-oxocyclohexen-1-yl]acetyl]-3-methyl-6-oxo-2H-pyran-3-yl]propanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9867 98.67%
Caco-2 - 0.7261 72.61%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8377 83.77%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior - 0.3748 37.48%
OATP1B3 inhibitior - 0.3132 31.32%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9842 98.42%
P-glycoprotein inhibitior + 0.8323 83.23%
P-glycoprotein substrate + 0.5923 59.23%
CYP3A4 substrate + 0.6735 67.35%
CYP2C9 substrate - 0.5928 59.28%
CYP2D6 substrate - 0.8939 89.39%
CYP3A4 inhibition - 0.5345 53.45%
CYP2C9 inhibition - 0.6753 67.53%
CYP2C19 inhibition - 0.7878 78.78%
CYP2D6 inhibition - 0.9376 93.76%
CYP1A2 inhibition - 0.8911 89.11%
CYP2C8 inhibition + 0.6782 67.82%
CYP inhibitory promiscuity - 0.8007 80.07%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9228 92.28%
Carcinogenicity (trinary) Non-required 0.5695 56.95%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.9328 93.28%
Skin irritation - 0.6821 68.21%
Skin corrosion - 0.9307 93.07%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6628 66.28%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.5177 51.77%
skin sensitisation - 0.8157 81.57%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6845 68.45%
Acute Oral Toxicity (c) I 0.4548 45.48%
Estrogen receptor binding + 0.8115 81.15%
Androgen receptor binding + 0.6221 62.21%
Thyroid receptor binding + 0.5963 59.63%
Glucocorticoid receptor binding + 0.7996 79.96%
Aromatase binding - 0.4877 48.77%
PPAR gamma + 0.8091 80.91%
Honey bee toxicity - 0.8097 80.97%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9814 98.14%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.11% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.07% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.84% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 95.40% 90.17%
CHEMBL4040 P28482 MAP kinase ERK2 92.94% 83.82%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.48% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.12% 96.00%
CHEMBL340 P08684 Cytochrome P450 3A4 86.37% 91.19%
CHEMBL2581 P07339 Cathepsin D 85.80% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.73% 97.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.51% 99.17%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 82.62% 80.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.23% 81.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.39% 99.23%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.31% 91.07%

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.
Xylocarpus granatum

Cross-Links

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PubChem 101848633
LOTUS LTS0010108
wikiData Q105122695