Scedapin G

Details

Top
Internal ID afd844ba-f363-4976-978e-7d23c21d0f2e
Taxonomy Lignans, neolignans and related compounds
IUPAC Name N-[(2S)-1-(4-methoxyphenyl)-3-oxo-4-(3,4,5-trimethoxyphenyl)butan-2-yl]formamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H25NO6/c1-25-16-7-5-14(6-8-16)9-17(22-13-23)18(24)10-15-11-19(26-2)21(28-4)20(12-15)27-3/h5-8,11-13,17H,9-10H2,1-4H3,(H,22,23)/t17-/m0/s1
InChI Key ISLZSBCNTPPXAF-KRWDZBQOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C21H25NO6
Molecular Weight 387.40 g/mol
Exact Mass 387.16818752 g/mol
Topological Polar Surface Area (TPSA) 83.10 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.19
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Scedapin G

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.5506 55.06%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7293 72.93%
OATP2B1 inhibitior - 0.8633 86.33%
OATP1B1 inhibitior + 0.8343 83.43%
OATP1B3 inhibitior + 0.9371 93.71%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.8426 84.26%
P-glycoprotein inhibitior + 0.8410 84.10%
P-glycoprotein substrate - 0.7632 76.32%
CYP3A4 substrate + 0.5640 56.40%
CYP2C9 substrate - 0.7778 77.78%
CYP2D6 substrate - 0.7341 73.41%
CYP3A4 inhibition + 0.7687 76.87%
CYP2C9 inhibition - 0.8937 89.37%
CYP2C19 inhibition - 0.6534 65.34%
CYP2D6 inhibition - 0.8520 85.20%
CYP1A2 inhibition + 0.6279 62.79%
CYP2C8 inhibition + 0.6154 61.54%
CYP inhibitory promiscuity + 0.5733 57.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8511 85.11%
Carcinogenicity (trinary) Non-required 0.6347 63.47%
Eye corrosion - 0.9926 99.26%
Eye irritation - 0.9296 92.96%
Skin irritation - 0.8603 86.03%
Skin corrosion - 0.9681 96.81%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8120 81.20%
Micronuclear + 0.7218 72.18%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.9476 94.76%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6810 68.10%
Acute Oral Toxicity (c) III 0.7087 70.87%
Estrogen receptor binding + 0.7891 78.91%
Androgen receptor binding + 0.5656 56.56%
Thyroid receptor binding + 0.6782 67.82%
Glucocorticoid receptor binding + 0.6732 67.32%
Aromatase binding + 0.5426 54.26%
PPAR gamma + 0.8040 80.40%
Honey bee toxicity - 0.8818 88.18%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.8768 87.68%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 97.26% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 96.89% 90.20%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.34% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.51% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.28% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.85% 94.45%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.41% 95.50%
CHEMBL2535 P11166 Glucose transporter 90.38% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.15% 86.33%
CHEMBL1741221 Q9Y4P1 Cysteine protease ATG4B 85.98% 87.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.82% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.75% 85.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.18% 92.62%
CHEMBL4208 P20618 Proteasome component C5 84.16% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.19% 96.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.05% 95.89%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.93% 96.95%
CHEMBL340 P08684 Cytochrome P450 3A4 81.86% 91.19%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.44% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.79% 91.07%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.71% 97.21%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.51% 94.00%

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.
There are no matching plants.

Cross-Links

Top
PubChem 139591089
LOTUS LTS0167753
wikiData Q105119623