Noricaritin

Details

Top
Internal ID 35cc7ec7-0c14-4a31-8f8a-eb99706bbe0a
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > 8-prenylated flavones
IUPAC Name 3,5,7-trihydroxy-8-(3-hydroxy-3-methylbutyl)-2-(4-hydroxyphenyl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H20O7/c1-20(2,26)8-7-12-13(22)9-14(23)15-16(24)17(25)18(27-19(12)15)10-3-5-11(21)6-4-10/h3-6,9,21-23,25-26H,7-8H2,1-2H3
InChI Key CTGVBHDTGZUEJZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H20O7
Molecular Weight 372.40 g/mol
Exact Mass 372.12090297 g/mol
Topological Polar Surface Area (TPSA) 127.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.99
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 4

Synonyms

Top
3,5,7-trihydroxy-8-(3-hydroxy-3-methylbutyl)-2-(4-hydroxyphenyl)chromen-4-one
RefChem:1092584
5240-95-9
NOR-ICARITIN
3,5,7-trihydroxy-8-(3-hydroxy-3-methylbutyl)-2-(4-hydroxyphenyl)-4h-chromen-4-one
MFCD28975884
orb1698423
SCHEMBL4213916
SCHEMBL29754704
FAA24095
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Noricaritin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9625 96.25%
Caco-2 - 0.5419 54.19%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7107 71.07%
OATP2B1 inhibitior + 0.5838 58.38%
OATP1B1 inhibitior + 0.7804 78.04%
OATP1B3 inhibitior + 0.9268 92.68%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.9037 90.37%
BSEP inhibitior + 0.7396 73.96%
P-glycoprotein inhibitior - 0.6156 61.56%
P-glycoprotein substrate - 0.5403 54.03%
CYP3A4 substrate + 0.5602 56.02%
CYP2C9 substrate - 0.5797 57.97%
CYP2D6 substrate - 0.8350 83.50%
CYP3A4 inhibition + 0.5912 59.12%
CYP2C9 inhibition - 0.7073 70.73%
CYP2C19 inhibition - 0.7711 77.11%
CYP2D6 inhibition - 0.8293 82.93%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition + 0.8066 80.66%
CYP inhibitory promiscuity - 0.7355 73.55%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6767 67.67%
Eye corrosion - 0.9915 99.15%
Eye irritation + 0.6358 63.58%
Skin irritation - 0.7141 71.41%
Skin corrosion - 0.8894 88.94%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5245 52.45%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.5967 59.67%
skin sensitisation - 0.8432 84.32%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.8367 83.67%
Acute Oral Toxicity (c) III 0.5875 58.75%
Estrogen receptor binding + 0.8909 89.09%
Androgen receptor binding + 0.8548 85.48%
Thyroid receptor binding + 0.6387 63.87%
Glucocorticoid receptor binding + 0.8886 88.86%
Aromatase binding + 0.7891 78.91%
PPAR gamma + 0.9180 91.80%
Honey bee toxicity - 0.8777 87.77%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9445 94.45%

Targets

Top

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 99.16% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.63% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.82% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 93.76% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.59% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.76% 94.00%
CHEMBL242 Q92731 Estrogen receptor beta 88.30% 98.35%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.52% 86.92%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.44% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.26% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.24% 94.45%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 83.97% 90.93%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 82.21% 95.64%
CHEMBL3194 P02766 Transthyretin 81.59% 90.71%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.47% 91.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.39% 99.17%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 80.54% 92.68%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.21% 93.65%

Plants that contains it

Top
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.
Epimedium brevicornu
Phellodendron amurense

Cross-Links

Top
PubChem 14427423
NPASS NPC150939
LOTUS LTS0160977
wikiData Q104969783