SMA-245
SMA-245 is an inhibitor of Filovirus glycoproteins, acting on Ebola virus (EBOV) and Marburg virus (MARV). SMA-245 blocks the endosomal membrane fusion step of filoviruses by binding to the EBOV GP1/GP2 fusion loop. SMA-245 inhibits MARV viral entry. SMA-245 can be used in research related to filovirus infections.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 分子式: C29H32N2O2
- 分子量:440.58
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
製品説明
IC50 & Target
[1]|
EBOV |
MARV |
Cellular Effect
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A549 | CC50 |
6.8 μM
|
Cytotoxicity against human A549 lung epithelial cells measured via CellTiter-Glo Luminescent Cell Viability Assay after 48 h incubation.
Cytotoxicity against human A549 lung epithelial cells measured via CellTiter-Glo Luminescent Cell Viability Assay after 48 h incubation.
|
42475249 |
| HeLa | CC50 |
4.6 μM
|
Cytotoxicity against human HeLa cervical cancer cells measured via CellTiter-Glo Luminescent Cell Viability Assay after 48 h incubation.
Cytotoxicity against human HeLa cervical cancer cells measured via CellTiter-Glo Luminescent Cell Viability Assay after 48 h incubation.
|
42475249 |
体外実験
SMA-245 (compound 41) (48 h) potently inhibits pEBOV entry in A549 cells with an EC50 of 0.040 μM, also inhibits pMARV, pSUDV, and pTAFV entry, shows no activity against pBDBV, and has low activity against non-filovirus pseudoviruses[1].
SMA-245 (40 h infection incubation; 48 h cytotoxicity incubation) potently inhibits infectious EBOV replication in HeLa cells with an EC50 of 0.04 μM and infectious MARV replication with an EC50 of 0.38 μM, with selectivity indices of 120 and 12, respectively[1].
SMA-245 moderately inhibits hERG potassium channels with an IC50 of 2.93 μM, representing a potential cardiac safety concern[1].
SMA-245 has excellent plasma stability in human and mouse, high stability in human liver microsomes, moderate stability in mouse liver microsomes, and low to moderate inhibition of major CYP450 isoforms at 10 μM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Parmacokinetics
体内実験
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
化学情報
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分子量 440.58
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分子式 C29H32N2O2
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SMILES
COC1=CC2=C(C(C(CC2)C3=CC=CC=C3)C4=CC=C(C=C4)NC(C5CCNCC5)=O)C=C1
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)