Lespeflorin C4

Details

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Internal ID ed01feb8-d918-4610-b6e7-5580e5e62191
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Cinnamylphenols
IUPAC Name (2S)-2-hydroxy-1-[4-hydroxy-2-methoxy-5-(3-methylbut-2-enyl)phenyl]-3-(4-methoxyphenyl)propan-1-one
SMILES (Canonical) CC(=CCC1=CC(=C(C=C1O)OC)C(=O)C(CC2=CC=C(C=C2)OC)O)C
SMILES (Isomeric) CC(=CCC1=CC(=C(C=C1O)OC)C(=O)[C@H](CC2=CC=C(C=C2)OC)O)C
InChI InChI=1S/C22H26O5/c1-14(2)5-8-16-12-18(21(27-4)13-19(16)23)22(25)20(24)11-15-6-9-17(26-3)10-7-15/h5-7,9-10,12-13,20,23-24H,8,11H2,1-4H3/t20-/m0/s1
InChI Key GHGQPDUKAGNTSF-FQEVSTJZSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H26O5
Molecular Weight 370.40 g/mol
Exact Mass 370.17802393 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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CHEMBL556260

2D Structure

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2D Structure of Lespeflorin C4

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.7465 74.65%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7585 75.85%
OATP2B1 inhibitior - 0.8613 86.13%
OATP1B1 inhibitior + 0.9212 92.12%
OATP1B3 inhibitior + 0.9119 91.19%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9843 98.43%
P-glycoprotein inhibitior + 0.8752 87.52%
P-glycoprotein substrate - 0.7221 72.21%
CYP3A4 substrate + 0.5203 52.03%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7232 72.32%
CYP3A4 inhibition - 0.7876 78.76%
CYP2C9 inhibition - 0.5102 51.02%
CYP2C19 inhibition + 0.8298 82.98%
CYP2D6 inhibition - 0.5925 59.25%
CYP1A2 inhibition + 0.7223 72.23%
CYP2C8 inhibition - 0.6212 62.12%
CYP inhibitory promiscuity + 0.5861 58.61%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8571 85.71%
Carcinogenicity (trinary) Non-required 0.7438 74.38%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.6553 65.53%
Skin irritation - 0.8035 80.35%
Skin corrosion - 0.9615 96.15%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7052 70.52%
Micronuclear - 0.5282 52.82%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.6402 64.02%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.7051 70.51%
Acute Oral Toxicity (c) III 0.5897 58.97%
Estrogen receptor binding + 0.9371 93.71%
Androgen receptor binding + 0.6547 65.47%
Thyroid receptor binding + 0.6903 69.03%
Glucocorticoid receptor binding + 0.9298 92.98%
Aromatase binding + 0.7169 71.69%
PPAR gamma + 0.7442 74.42%
Honey bee toxicity - 0.8468 84.68%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9895 98.95%

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 98.29% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.75% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.56% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.51% 99.17%
CHEMBL2535 P11166 Glucose transporter 95.06% 98.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 93.31% 95.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.22% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.77% 85.14%
CHEMBL3492 P49721 Proteasome Macropain subunit 91.05% 90.24%
CHEMBL4208 P20618 Proteasome component C5 90.96% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.93% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 90.84% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 90.32% 96.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.11% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.04% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.25% 92.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.09% 99.15%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 88.41% 97.21%
CHEMBL1255126 O15151 Protein Mdm4 87.93% 90.20%
CHEMBL3401 O75469 Pregnane X receptor 86.05% 94.73%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.29% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.15% 94.00%
CHEMBL340 P08684 Cytochrome P450 3A4 84.01% 91.19%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.27% 95.89%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.96% 91.71%
CHEMBL3714130 P46095 G-protein coupled receptor 6 81.14% 97.36%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.21% 91.07%

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 25243323
LOTUS LTS0259352
wikiData Q105008519