Lespeflorin C3

Details

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Internal ID a8e21de4-bc33-4608-b567-73c44276edac
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-hydroxyphenyl)propan-1-one
SMILES (Canonical) CC(=CCC1=CC(=C(C=C1O)OC)C(=O)C(CC2=CC=C(C=C2)O)O)C
SMILES (Isomeric) CC(=CCC1=CC(=C(C=C1O)OC)C(=O)[C@H](CC2=CC=C(C=C2)O)O)C
InChI InChI=1S/C21H24O5/c1-13(2)4-7-15-11-17(20(26-3)12-18(15)23)21(25)19(24)10-14-5-8-16(22)9-6-14/h4-6,8-9,11-12,19,22-24H,7,10H2,1-3H3/t19-/m0/s1
InChI Key XTDORSAGLFPXGX-IBGZPJMESA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H24O5
Molecular Weight 356.40 g/mol
Exact Mass 356.16237386 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.40
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

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CHEBI:66564
(2S)-2-hydroxy-1-[4-hydroxy-2-methoxy-5-(3-methylbut-2-en-1-yl)phenyl]-3-(4-hydroxyphenyl)propan-1-one
CHEMBL560625
DTXSID901112598
Q27135177
(2S)-2-Hydroxy-1-[4-hydroxy-2-methoxy-5-(3-methyl-2-buten-1-yl)phenyl]-3-(4-hydroxyphenyl)-1-propanone
(2S)-2-hydroxy-1-[4-hydroxy-2-methoxy-5-(3-methylbut-2-enyl)phenyl]-3-(4-hydroxyphenyl)propan-1-one
1108717-59-4

2D Structure

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2D Structure of Lespeflorin C3

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 + 0.6390 63.90%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7585 75.85%
OATP2B1 inhibitior - 0.5765 57.65%
OATP1B1 inhibitior + 0.9074 90.74%
OATP1B3 inhibitior + 0.9119 91.19%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9776 97.76%
P-glycoprotein inhibitior + 0.6819 68.19%
P-glycoprotein substrate - 0.6498 64.98%
CYP3A4 substrate + 0.5126 51.26%
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 + 0.5220 52.20%
CYP inhibitory promiscuity + 0.5861 58.61%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8571 85.71%
Carcinogenicity (trinary) Non-required 0.7438 74.38%
Eye corrosion - 0.9906 99.06%
Eye irritation + 0.5415 54.15%
Skin irritation - 0.8035 80.35%
Skin corrosion - 0.9615 96.15%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4260 42.60%
Micronuclear - 0.5282 52.82%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.6402 64.02%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.6238 62.38%
Acute Oral Toxicity (c) III 0.5897 58.97%
Estrogen receptor binding + 0.9304 93.04%
Androgen receptor binding + 0.6689 66.89%
Thyroid receptor binding + 0.6737 67.37%
Glucocorticoid receptor binding + 0.8810 88.10%
Aromatase binding + 0.7250 72.50%
PPAR gamma + 0.7837 78.37%
Honey bee toxicity - 0.7927 79.27%
Biodegradation - 0.9000 90.00%
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
CHEMBL2581 P07339 Cathepsin D 97.66% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.37% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.53% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.51% 99.17%
CHEMBL2535 P11166 Glucose transporter 95.34% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.29% 94.45%
CHEMBL1255126 O15151 Protein Mdm4 94.56% 90.20%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.53% 85.14%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 91.07% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.04% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 90.76% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 90.53% 97.21%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 88.19% 95.89%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 88.07% 91.71%
CHEMBL3401 O75469 Pregnane X receptor 86.57% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.17% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.07% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 83.79% 91.19%
CHEMBL2413 P32246 C-C chemokine receptor type 1 83.21% 89.50%
CHEMBL4208 P20618 Proteasome component C5 82.74% 90.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 82.50% 90.24%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.81% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.35% 92.62%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 80.59% 92.29%

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 25243322
NPASS NPC245482
ChEMBL CHEMBL560625
LOTUS LTS0191976
wikiData Q27135177