(+)-mitorubrinic acid B

Details

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Internal ID b6f48d17-c315-46fe-b914-f209795a2d9f
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > p-Hydroxybenzoic acid esters > p-Hydroxybenzoic acid alkyl esters
IUPAC Name (E)-3-[(7R,8R)-8-(2,4-dihydroxy-6-methylbenzoyl)oxy-7-hydroxy-7-methyl-6-oxo-8H-isochromen-3-yl]prop-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H18O9/c1-10-5-12(22)8-15(23)18(10)20(27)30-19-14-9-29-13(3-4-17(25)26)6-11(14)7-16(24)21(19,2)28/h3-9,19,22-23,28H,1-2H3,(H,25,26)/b4-3+/t19-,21+/m1/s1
InChI Key KEFMWOFGFUZREC-MPTWLCKMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H18O9
Molecular Weight 414.40 g/mol
Exact Mass 414.09508215 g/mol
Topological Polar Surface Area (TPSA) 151.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.63
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (+)-mitorubrinic acid B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9562 95.62%
Caco-2 - 0.6942 69.42%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6858 68.58%
OATP2B1 inhibitior - 0.5739 57.39%
OATP1B1 inhibitior + 0.8408 84.08%
OATP1B3 inhibitior + 0.9323 93.23%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8270 82.70%
P-glycoprotein inhibitior - 0.5188 51.88%
P-glycoprotein substrate - 0.6535 65.35%
CYP3A4 substrate + 0.6775 67.75%
CYP2C9 substrate - 0.8036 80.36%
CYP2D6 substrate - 0.8956 89.56%
CYP3A4 inhibition - 0.7664 76.64%
CYP2C9 inhibition + 0.5907 59.07%
CYP2C19 inhibition - 0.5934 59.34%
CYP2D6 inhibition - 0.8605 86.05%
CYP1A2 inhibition - 0.6815 68.15%
CYP2C8 inhibition + 0.7489 74.89%
CYP inhibitory promiscuity + 0.6304 63.04%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9918 99.18%
Carcinogenicity (trinary) Danger 0.4404 44.04%
Eye corrosion - 0.9843 98.43%
Eye irritation - 0.6701 67.01%
Skin irritation - 0.5762 57.62%
Skin corrosion - 0.9207 92.07%
Ames mutagenesis - 0.5654 56.54%
Human Ether-a-go-go-Related Gene inhibition - 0.3808 38.08%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.7131 71.31%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.6383 63.83%
Acute Oral Toxicity (c) III 0.5400 54.00%
Estrogen receptor binding + 0.8137 81.37%
Androgen receptor binding + 0.7353 73.53%
Thyroid receptor binding + 0.6462 64.62%
Glucocorticoid receptor binding + 0.6772 67.72%
Aromatase binding + 0.5677 56.77%
PPAR gamma + 0.6818 68.18%
Honey bee toxicity - 0.7863 78.63%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9807 98.07%

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 98.80% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.45% 86.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.03% 94.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.01% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.99% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 91.24% 94.73%
CHEMBL3194 P02766 Transthyretin 89.91% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.76% 95.56%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 88.87% 81.11%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 87.48% 95.70%
CHEMBL340 P08684 Cytochrome P450 3A4 87.30% 91.19%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.04% 99.23%
CHEMBL1929 P47989 Xanthine dehydrogenase 85.83% 96.12%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.68% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.76% 96.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.90% 91.07%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.35% 94.80%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 163040080
LOTUS LTS0053865
wikiData Q105139939