Lespeflorin A2

Details

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Internal ID a6425a46-c00b-4e78-977e-01fd31febb58
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 8-prenylated flavans > 8-prenylated flavanones
IUPAC Name (2S)-7-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
SMILES (Canonical) CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)OC)O)C
SMILES (Isomeric) CC(=CCC1=C(C=CC2=C1O[C@@H](CC2=O)C3=CC=C(C=C3)OC)O)C
InChI InChI=1S/C21H22O4/c1-13(2)4-9-16-18(22)11-10-17-19(23)12-20(25-21(16)17)14-5-7-15(24-3)8-6-14/h4-8,10-11,20,22H,9,12H2,1-3H3/t20-/m0/s1
InChI Key PAILWWPOJHGXTM-FQEVSTJZSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H22O4
Molecular Weight 338.40 g/mol
Exact Mass 338.15180918 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.62
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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CHEMBL551902

2D Structure

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2D Structure of Lespeflorin A2

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9964 99.64%
Caco-2 + 0.8738 87.38%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8163 81.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8900 89.00%
OATP1B3 inhibitior + 0.9163 91.63%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7904 79.04%
P-glycoprotein inhibitior + 0.7694 76.94%
P-glycoprotein substrate - 0.8123 81.23%
CYP3A4 substrate + 0.5916 59.16%
CYP2C9 substrate - 0.8006 80.06%
CYP2D6 substrate - 0.7235 72.35%
CYP3A4 inhibition - 0.7858 78.58%
CYP2C9 inhibition + 0.6960 69.60%
CYP2C19 inhibition + 0.9209 92.09%
CYP2D6 inhibition - 0.7812 78.12%
CYP1A2 inhibition + 0.7125 71.25%
CYP2C8 inhibition - 0.7452 74.52%
CYP inhibitory promiscuity + 0.8540 85.40%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9613 96.13%
Carcinogenicity (trinary) Non-required 0.7040 70.40%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.8236 82.36%
Skin irritation - 0.7925 79.25%
Skin corrosion - 0.9683 96.83%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4341 43.41%
Micronuclear - 0.5341 53.41%
Hepatotoxicity - 0.5948 59.48%
skin sensitisation - 0.8254 82.54%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.4884 48.84%
Acute Oral Toxicity (c) III 0.6425 64.25%
Estrogen receptor binding + 0.9105 91.05%
Androgen receptor binding + 0.8044 80.44%
Thyroid receptor binding + 0.7360 73.60%
Glucocorticoid receptor binding + 0.7631 76.31%
Aromatase binding + 0.5234 52.34%
PPAR gamma + 0.7316 73.16%
Honey bee toxicity - 0.8093 80.93%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9838 98.38%

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 99.42% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.85% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.76% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.71% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.35% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.84% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.02% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.34% 99.15%
CHEMBL221 P23219 Cyclooxygenase-1 88.41% 90.17%
CHEMBL4208 P20618 Proteasome component C5 88.33% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.77% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.13% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.88% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.47% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.18% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 82.82% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.68% 96.95%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.80% 86.92%

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.
Lespedeza floribunda

Cross-Links

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PubChem 25243165
NPASS NPC149026
ChEMBL CHEMBL551902
LOTUS LTS0101914
wikiData Q105204544