Dichotomoside A

Details

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Internal ID 313ae8e1-bb2c-4126-b5e5-ff56a4af76b7
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name 3-[3-[5-(2-carboxyethyl)-3-methoxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-4-hydroxy-5-methoxyphenyl]propanoic acid
SMILES (Canonical) COC1=CC(=CC(=C1O)C2=C(C(=CC(=C2)CCC(=O)O)OC)OC3C(C(C(C(O3)CO)O)O)O)CCC(=O)O
SMILES (Isomeric) COC1=CC(=CC(=C1O)C2=C(C(=CC(=C2)CCC(=O)O)OC)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)CCC(=O)O
InChI InChI=1S/C26H32O13/c1-36-16-9-12(3-5-19(28)29)7-14(21(16)32)15-8-13(4-6-20(30)31)10-17(37-2)25(15)39-26-24(35)23(34)22(33)18(11-27)38-26/h7-10,18,22-24,26-27,32-35H,3-6,11H2,1-2H3,(H,28,29)(H,30,31)/t18-,22-,23+,24-,26+/m1/s1
InChI Key CMWSNZIIKSIMDM-OKOABTSWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C26H32O13
Molecular Weight 552.50 g/mol
Exact Mass 552.18429107 g/mol
Topological Polar Surface Area (TPSA) 213.00 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.29
H-Bond Acceptor 11
H-Bond Donor 7
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Dichotomoside A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6909 69.09%
Caco-2 - 0.8708 87.08%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7222 72.22%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.7825 78.25%
OATP1B3 inhibitior + 0.9320 93.20%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8942 89.42%
P-glycoprotein inhibitior - 0.4323 43.23%
P-glycoprotein substrate - 0.7707 77.07%
CYP3A4 substrate + 0.6176 61.76%
CYP2C9 substrate - 0.8044 80.44%
CYP2D6 substrate - 0.8453 84.53%
CYP3A4 inhibition - 0.8151 81.51%
CYP2C9 inhibition - 0.7922 79.22%
CYP2C19 inhibition - 0.9289 92.89%
CYP2D6 inhibition - 0.9332 93.32%
CYP1A2 inhibition - 0.8613 86.13%
CYP2C8 inhibition + 0.7099 70.99%
CYP inhibitory promiscuity - 0.9078 90.78%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.7938 79.38%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.9240 92.40%
Skin irritation - 0.8431 84.31%
Skin corrosion - 0.9474 94.74%
Ames mutagenesis - 0.7570 75.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4774 47.74%
Micronuclear - 0.5567 55.67%
Hepatotoxicity - 0.7948 79.48%
skin sensitisation - 0.9213 92.13%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.9239 92.39%
Acute Oral Toxicity (c) III 0.7522 75.22%
Estrogen receptor binding + 0.8206 82.06%
Androgen receptor binding - 0.5453 54.53%
Thyroid receptor binding - 0.5382 53.82%
Glucocorticoid receptor binding + 0.7246 72.46%
Aromatase binding + 0.5269 52.69%
PPAR gamma + 0.6466 64.66%
Honey bee toxicity - 0.8430 84.30%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7704 77.04%
Fish aquatic toxicity + 0.6697 66.97%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.69% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.71% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.58% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 97.13% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.76% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.98% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 87.55% 90.20%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.81% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.05% 89.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.75% 95.50%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.95% 95.89%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.61% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 81.85% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.43% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.26% 95.56%

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.
Stellaria dichotoma

Cross-Links

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PubChem 11203673
NPASS NPC197063
LOTUS LTS0237001
wikiData Q104965307