Curculigine A

Details

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Internal ID 55ad678b-3e43-47dd-b272-27f93f0e8c93
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name (2R,3R,4S,5S,6R)-2-[[(2R,3S,4S,5R,6S)-6-(2,4-dichloro-5-methoxy-3-methylphenoxy)-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H28Cl2O12/c1-6-11(21)7(30-2)3-8(12(6)22)32-20-18(29)16(27)14(25)10(34-20)5-31-19-17(28)15(26)13(24)9(4-23)33-19/h3,9-10,13-20,23-29H,4-5H2,1-2H3/t9-,10-,13-,14-,15+,16+,17-,18-,19-,20-/m1/s1
InChI Key XBVNHJLYWKRWAX-RPDXMDMVSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C20H28Cl2O12
Molecular Weight 531.30 g/mol
Exact Mass 530.0957817 g/mol
Topological Polar Surface Area (TPSA) 188.00 Ų
XlogP -0.80
Atomic LogP (AlogP) -1.69
H-Bond Acceptor 12
H-Bond Donor 7
Rotatable Bonds 7

Synonyms

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Curculigine A
Curculigin A
DTXSID40911909
2,4-Dichloro-5-methoxy-3-methylphenyl 6-O-hexopyranosylhexopyranoside

2D Structure

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2D Structure of Curculigine A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7299 72.99%
Caco-2 - 0.8603 86.03%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.5845 58.45%
OATP2B1 inhibitior - 0.8612 86.12%
OATP1B1 inhibitior + 0.8698 86.98%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.5447 54.47%
P-glycoprotein inhibitior - 0.7262 72.62%
P-glycoprotein substrate - 0.8638 86.38%
CYP3A4 substrate + 0.5603 56.03%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8154 81.54%
CYP3A4 inhibition - 0.9307 93.07%
CYP2C9 inhibition - 0.8131 81.31%
CYP2C19 inhibition - 0.7035 70.35%
CYP2D6 inhibition - 0.8846 88.46%
CYP1A2 inhibition - 0.8105 81.05%
CYP2C8 inhibition - 0.5861 58.61%
CYP inhibitory promiscuity - 0.5219 52.19%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8177 81.77%
Carcinogenicity (trinary) Non-required 0.5833 58.33%
Eye corrosion - 0.9869 98.69%
Eye irritation - 0.9590 95.90%
Skin irritation - 0.8080 80.80%
Skin corrosion - 0.9396 93.96%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4191 41.91%
Micronuclear - 0.6082 60.82%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.8535 85.35%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.6821 68.21%
Acute Oral Toxicity (c) III 0.6567 65.67%
Estrogen receptor binding + 0.7550 75.50%
Androgen receptor binding - 0.5819 58.19%
Thyroid receptor binding + 0.6276 62.76%
Glucocorticoid receptor binding - 0.5586 55.86%
Aromatase binding + 0.7037 70.37%
PPAR gamma + 0.6997 69.97%
Honey bee toxicity - 0.8713 87.13%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.6391 63.91%

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 96.99% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.21% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 91.47% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.26% 94.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.27% 86.92%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 89.49% 89.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.52% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.02% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.00% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.77% 99.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.38% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.60% 95.56%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.20% 96.90%

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.
Curculigo orchioides

Cross-Links

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PubChem 183146
LOTUS LTS0087213
wikiData Q82882128