Cyanidin 3-lathyroside

Details

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Internal ID 072e4e49-126d-47ba-9b19-74f04a69eaa8
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Anthocyanins > Anthocyanidin-3-O-glycosides
IUPAC Name (2S,3R,5R)-2-[(2S,5R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol
SMILES (Canonical) C1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)CO)O)O)O)O)O
SMILES (Isomeric) C1[C@H](C([C@H]([C@@H](O1)OC2[C@@H](OC([C@@H](C2O)O)CO)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O
InChI InChI=1S/C26H28O15/c27-7-18-20(34)21(35)24(41-25-22(36)19(33)15(32)8-37-25)26(40-18)39-17-6-11-13(30)4-10(28)5-16(11)38-23(17)9-1-2-12(29)14(31)3-9/h1-6,15,18-22,24-27,32-36H,7-8H2,(H3-,28,29,30,31)/p+1/t15-,18?,19?,20+,21?,22-,24?,25+,26-/m1/s1
InChI Key ZPPQIOUITZSYAO-HVHHODJLSA-O
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H29O15+
Molecular Weight 581.50 g/mol
Exact Mass 581.15064521 g/mol
Topological Polar Surface Area (TPSA) 240.00 Ų
XlogP 0.00
Atomic LogP (AlogP) -1.15
H-Bond Acceptor 14
H-Bond Donor 10
Rotatable Bonds 6

Synonyms

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CHEBI:187411
LMPK12010096
(2S,3R,5R)-2-[(2S,5R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol

2D Structure

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2D Structure of Cyanidin 3-lathyroside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8094 80.94%
Caco-2 - 0.9201 92.01%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Nucleus 0.4922 49.22%
OATP2B1 inhibitior - 0.5579 55.79%
OATP1B1 inhibitior + 0.9120 91.20%
OATP1B3 inhibitior + 0.9359 93.59%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6465 64.65%
P-glycoprotein inhibitior - 0.5875 58.75%
P-glycoprotein substrate - 0.6414 64.14%
CYP3A4 substrate + 0.6494 64.94%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8268 82.68%
CYP3A4 inhibition - 0.9674 96.74%
CYP2C9 inhibition - 0.9451 94.51%
CYP2C19 inhibition - 0.8795 87.95%
CYP2D6 inhibition - 0.8992 89.92%
CYP1A2 inhibition - 0.9079 90.79%
CYP2C8 inhibition + 0.7661 76.61%
CYP inhibitory promiscuity - 0.8848 88.48%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6278 62.78%
Eye corrosion - 0.9930 99.30%
Eye irritation - 0.8897 88.97%
Skin irritation - 0.8130 81.30%
Skin corrosion - 0.9616 96.16%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6799 67.99%
Micronuclear + 0.6259 62.59%
Hepatotoxicity - 0.7998 79.98%
skin sensitisation - 0.9039 90.39%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.9233 92.33%
Acute Oral Toxicity (c) III 0.4867 48.67%
Estrogen receptor binding + 0.8136 81.36%
Androgen receptor binding + 0.6121 61.21%
Thyroid receptor binding + 0.6470 64.70%
Glucocorticoid receptor binding + 0.5508 55.08%
Aromatase binding + 0.7475 74.75%
PPAR gamma + 0.8036 80.36%
Honey bee toxicity - 0.6913 69.13%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.6534 65.34%

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 99.71% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.95% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.98% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.95% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.10% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.32% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.14% 92.94%
CHEMBL2581 P07339 Cathepsin D 89.87% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.43% 97.09%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 89.07% 95.78%
CHEMBL226 P30542 Adenosine A1 receptor 88.59% 95.93%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 88.42% 95.83%
CHEMBL1937 Q92769 Histone deacetylase 2 87.74% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.25% 86.33%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.23% 89.62%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.68% 94.45%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.02% 86.92%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.25% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.39% 99.17%
CHEMBL4208 P20618 Proteasome component C5 83.11% 90.00%
CHEMBL3714130 P46095 G-protein coupled receptor 6 81.49% 97.36%
CHEMBL3194 P02766 Transthyretin 81.00% 90.71%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 80.51% 92.68%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.28% 97.28%

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.
Fatsia japonica

Cross-Links

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PubChem 44256701
LOTUS LTS0110863
wikiData Q105381108