tricin 7-O-neohesperidoside

Details

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Internal ID 5adefc07-f302-4ee1-96d8-36c8ce086e47
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name 7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)chromen-4-one
SMILES (Canonical) CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C(=C5)OC)O)OC)O)CO)O)O)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]2[C@H]([C@@H]([C@H](O[C@H]2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C(=C5)OC)O)OC)O)CO)O)O)O)O)O
InChI InChI=1S/C29H34O16/c1-10-21(33)24(36)26(38)28(41-10)45-27-25(37)23(35)19(9-30)44-29(27)42-12-6-13(31)20-14(32)8-15(43-16(20)7-12)11-4-17(39-2)22(34)18(5-11)40-3/h4-8,10,19,21,23-31,33-38H,9H2,1-3H3/t10-,19+,21-,23+,24+,25-,26+,27+,28-,29+/m0/s1
InChI Key AIBMPOJXBGZIPQ-QWNFCSOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C29H34O16
Molecular Weight 638.60 g/mol
Exact Mass 638.18468499 g/mol
Topological Polar Surface Area (TPSA) 244.00 Ų
XlogP -0.30
Atomic LogP (AlogP) -1.08
H-Bond Acceptor 16
H-Bond Donor 8
Rotatable Bonds 8

Synonyms

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53766-40-8
Tricin 7-neohesperidoside
CHEBI:131777
DTXSID001309918
7-O-[alpha-L-rhamnosyl-(1->2)-beta-D-glucosyl]tricin
7-O-[alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranosyl]tricin
5-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-4-oxo-4H-1-benzopyran-7-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside
7-[(2-O-alpha-L-Rhamnopyranosyl-beta-D-glucopyranosyl)oxy]-4',5-dihydroxy-3',5'-dimethoxyflavone

2D Structure

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2D Structure of tricin 7-O-neohesperidoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5088 50.88%
Caco-2 - 0.8884 88.84%
Blood Brain Barrier - 0.8750 87.50%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.6030 60.30%
OATP2B1 inhibitior - 0.5795 57.95%
OATP1B1 inhibitior + 0.9214 92.14%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.6338 63.38%
P-glycoprotein inhibitior - 0.5572 55.72%
P-glycoprotein substrate + 0.6128 61.28%
CYP3A4 substrate + 0.6229 62.29%
CYP2C9 substrate - 0.8740 87.40%
CYP2D6 substrate - 0.8547 85.47%
CYP3A4 inhibition - 0.9371 93.71%
CYP2C9 inhibition - 0.9410 94.10%
CYP2C19 inhibition - 0.9438 94.38%
CYP2D6 inhibition - 0.9518 95.18%
CYP1A2 inhibition - 0.9134 91.34%
CYP2C8 inhibition + 0.6469 64.69%
CYP inhibitory promiscuity - 0.7474 74.74%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7050 70.50%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9238 92.38%
Skin irritation - 0.8406 84.06%
Skin corrosion - 0.9638 96.38%
Ames mutagenesis - 0.5364 53.64%
Human Ether-a-go-go-Related Gene inhibition + 0.7108 71.08%
Micronuclear + 0.6433 64.33%
Hepatotoxicity - 0.8250 82.50%
skin sensitisation - 0.9409 94.09%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.9366 93.66%
Acute Oral Toxicity (c) III 0.6685 66.85%
Estrogen receptor binding + 0.8204 82.04%
Androgen receptor binding - 0.4816 48.16%
Thyroid receptor binding + 0.5561 55.61%
Glucocorticoid receptor binding + 0.6284 62.84%
Aromatase binding + 0.6026 60.26%
PPAR gamma + 0.7552 75.52%
Honey bee toxicity - 0.6377 63.77%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.7605 76.05%

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 99.63% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.55% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.62% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.48% 85.14%
CHEMBL3714130 P46095 G-protein coupled receptor 6 96.40% 97.36%
CHEMBL1951 P21397 Monoamine oxidase A 96.31% 91.49%
CHEMBL2581 P07339 Cathepsin D 93.73% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.03% 86.33%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 89.46% 96.21%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.92% 86.92%
CHEMBL3194 P02766 Transthyretin 88.89% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.63% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.15% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.06% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 87.32% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.83% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.11% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.97% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.12% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.97% 97.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.77% 96.00%

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.
Phoenix dactylifera
Phoenix loureiroi var. loureiroi

Cross-Links

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PubChem 102158614
NPASS NPC180664
LOTUS LTS0188916
wikiData Q104912614