7-O-Demethylcelesticetin C

Details

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Internal ID ce4b5ca5-906e-44f8-bc70-181fa34365ba
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Proline and derivatives
IUPAC Name 2-[3,4,5-trihydroxy-6-[2-hydroxy-1-[(1-methylpyrrolidine-2-carbonyl)amino]propyl]oxan-2-yl]sulfanylethyl 2-aminobenzoate
SMILES (Canonical) CC(C(C1C(C(C(C(O1)SCCOC(=O)C2=CC=CC=C2N)O)O)O)NC(=O)C3CCCN3C)O
SMILES (Isomeric) CC(C(C1C(C(C(C(O1)SCCOC(=O)C2=CC=CC=C2N)O)O)O)NC(=O)C3CCCN3C)O
InChI InChI=1S/C23H35N3O8S/c1-12(27)16(25-21(31)15-8-5-9-26(15)2)20-18(29)17(28)19(30)23(34-20)35-11-10-33-22(32)13-6-3-4-7-14(13)24/h3-4,6-7,12,15-20,23,27-30H,5,8-11,24H2,1-2H3,(H,25,31)
InChI Key MCXVOLNKDLQSAY-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C23H35N3O8S
Molecular Weight 513.60 g/mol
Exact Mass 513.21448626 g/mol
Topological Polar Surface Area (TPSA) 200.00 Ų
XlogP 0.60
Atomic LogP (AlogP) -1.07
H-Bond Acceptor 11
H-Bond Donor 6
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-O-Demethylcelesticetin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9523 95.23%
Caco-2 - 0.8416 84.16%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.4542 45.42%
OATP2B1 inhibitior - 0.7194 71.94%
OATP1B1 inhibitior + 0.9107 91.07%
OATP1B3 inhibitior + 0.9305 93.05%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.5530 55.30%
P-glycoprotein inhibitior - 0.5560 55.60%
P-glycoprotein substrate + 0.7407 74.07%
CYP3A4 substrate + 0.6973 69.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8173 81.73%
CYP3A4 inhibition - 0.8428 84.28%
CYP2C9 inhibition - 0.6973 69.73%
CYP2C19 inhibition - 0.7689 76.89%
CYP2D6 inhibition - 0.8472 84.72%
CYP1A2 inhibition - 0.8702 87.02%
CYP2C8 inhibition - 0.6887 68.87%
CYP inhibitory promiscuity - 0.8751 87.51%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5964 59.64%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.9666 96.66%
Skin irritation - 0.7685 76.85%
Skin corrosion - 0.9315 93.15%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6455 64.55%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8638 86.38%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.6331 63.31%
Acute Oral Toxicity (c) III 0.6184 61.84%
Estrogen receptor binding + 0.7818 78.18%
Androgen receptor binding - 0.4885 48.85%
Thyroid receptor binding + 0.5344 53.44%
Glucocorticoid receptor binding - 0.5110 51.10%
Aromatase binding + 0.5671 56.71%
PPAR gamma + 0.6781 67.81%
Honey bee toxicity - 0.8164 81.64%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.8514 85.14%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.34% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 98.99% 90.17%
CHEMBL2581 P07339 Cathepsin D 98.13% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 97.77% 83.82%
CHEMBL4208 P20618 Proteasome component C5 94.84% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 93.09% 95.89%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.77% 91.11%
CHEMBL220 P22303 Acetylcholinesterase 92.13% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.74% 97.25%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.60% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.04% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.74% 97.09%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 87.98% 98.33%
CHEMBL3401 O75469 Pregnane X receptor 85.77% 94.73%
CHEMBL4227 P25090 Lipoxin A4 receptor 85.62% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.99% 93.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.76% 94.45%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 82.88% 95.17%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 82.16% 96.47%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.68% 91.07%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.51% 97.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.28% 96.00%
CHEMBL5028 O14672 ADAM10 81.14% 97.50%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.95% 89.62%
CHEMBL1944495 P28065 Proteasome subunit beta type-9 80.48% 97.50%
CHEMBL2535 P11166 Glucose transporter 80.23% 98.75%
CHEMBL2782 P35610 Acyl coenzyme A:cholesterol acyltransferase 1 80.06% 91.65%

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 139587630
LOTUS LTS0119369
wikiData Q77570764