Imidazopyridines
Medchemexpress LLC Cxcr7 antagonist-1 | 1613021-99-0 | 99.9% | 390.41 | 50 MG
CXCR7 antagonist-1 is a CXCR7 antagonist that inhibits the binding of the SDF-1 chemokine (also known as the CXCL12 chemokine) or I-TAC (also known as CXCL11) to the chemokine receptor CXCR7. It is useful in preventing tumor cell proliferation, tumor formation, inflammatory diseases, and many other diseases.
- Inhibits binding of SDF-1 (CXCL12) or I-TAC (CXCL11) to the chemokine receptor CXCR7.
- Useful in preventing tumor cell proliferation and formation.
- Applied in inflammatory diseases.
- Restores CXCL11 or RSV infection-induced β2-adrenergic receptor (β2AR) downregulation in infant airway smooth muscle cells.
- Inhibits airway smooth muscle relaxation induced by RSV-infection in BALB/c mouse models.
![eMolecules 1404480-51-8 | 6-Bromoimidazo[1,2-a]pyrazine-3-carboxylic acid | MFCD27635053 | 250mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502133328.JPG-250.jpg)
eMolecules 1404480-51-8 | 6-Bromoimidazo[1,2-a]pyrazine-3-carboxylic acid | MFCD27635053 | 250mg
Ambeed | 1-(Trifluoromethylthio)pyrrolidine-25-dione | 1g | 714089801 | A986831 | 183267-04-1 | MFCD30187362 | 199.150 | C5H4F3NO2S
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![eMolecules 1221791-93-0 | 8-Bromoimidazo[1,2-a]pyridine-6-carbonitrile | Apollo Scientific | MFCD14584821 | 222.045 | C8H4BrN3 | 95.000 | Brc1cc(cn2ccnc12)C#N | 1g | 562429762](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502152137.JPG-250.jpg)
eMolecules 1221791-93-0 | 8-Bromoimidazo[1,2-a]pyridine-6-carbonitrile | Apollo Scientific | MFCD14584821 | 222.045 | C8H4BrN3 | 95.000 | Brc1cc(cn2ccnc12)C#N | 1g | 562429762
8-Bromoimidazo[1,2-a]pyridine-6-carbonitrile | Apollo Scientific | 1221791-93-0 | MFCD14584821 | 222.045 | C8H4BrN3 | 95.000 | Brc1cc(cn2ccnc12)C#N | 1g | 562429762
Medchemexpress LLC Odoroside A | 12738-19-1 | 10 MG
Odoroside A is an active ingredient extracted from the leaves of Nerium oleander Linn. It exhibits anti-cancer activity by inducing apoptosis and cell cycle arrest through the ROS/p53 signaling pathway, leading to tumor cell death.
- Active ingredient extracted from Nerium oleander Linn
- Exhibits anti-cancer activity
- Induces apoptosis and cell cycle arrest
- Works via the ROS/p53 signaling pathway
- Leads to tumor cell death
- High purity of 99.73%
- Molecular weight: 518.68
- Molecular formula: C₃₀H₄₆O₇
- Appearance: White to off-white solid
- Soluble in DMSO
- Targeted pathway: Apoptosis
- For research use only
Medchemexpress LLC CXCR7 antagonist-1 | 1613021-99-0 | 99.85% | 390.41 | 100 MG
CXCR7 antagonist-1 is a CXCR7 antagonist that inhibits the binding of the SDF-1 chemokine (CXCL12) or I-TAC (CXCL11) to the chemokine receptor CXCR7. It is useful in preventing tumor cell proliferation, tumor formation, inflammatory diseases, and many other diseases.
- Inhibits SDF-1 and I-TAC chemokine binding
- Useful in preventing tumor cell proliferation
- Useful in preventing tumor formation
- Useful in preventing inflammatory diseases
- Useful in preventing many other diseases
![eMolecules 133240-06-9 | 2-Ethyl-5,7-dimethyl-1H-imidazo[4,5-b]pyridine | AA Blocks LLC | MFCD01632103 | 175.235 | C10H13N3 | 0.000 | CCc1nc2c(C)cc(C)nc2[nH]1 | 250mg | 586001880](https://assets.fishersci.com/TFS-Assets/CCG/product-images/NC3963055.jpg-250.jpg)
eMolecules 133240-06-9 | 2-Ethyl-5,7-dimethyl-1H-imidazo[4,5-b]pyridine | AA Blocks LLC | MFCD01632103 | 175.235 | C10H13N3 | 0.000 | CCc1nc2c(C)cc(C)nc2[nH]1 | 250mg | 586001880
2-Ethyl-5,7-dimethyl-1H-imidazo[4,5-b]pyridine | AA Blocks LLC | 133240-06-9 | MFCD01632103 | 175.235 | C10H13N3 | 0.000 | CCc1nc2c(C)cc(C)nc2[nH]1 | 250mg | 586001880
eMolecules 163105-89-3 | 6-Methoxy-pyridine-3-boronic acid | J & W PharmLab LLC | MFCD02093044 | 152.940 | C6H8BNO3 | 96.000 | COc1ccc(cn1)B(O)O | 25g | 304166044
6-Methoxy-pyridine-3-boronic acid | J & W PharmLab LLC | 163105-89-3 | MFCD02093044 | 152.940 | C6H8BNO3 | 96.000 | COc1ccc(cn1)B(O)O | 25g | 304166044
Medchemexpress LLC Elsulfavirine | 868046-19-9 | MFCD32215300 | 99.9% | 629.28 g·mol⁻¹ | C24H17BrCl2FN3O5S | 5 MG
Elsulfavirine is a non-nucleoside reverse transcriptase inhibitor (NNRTI) investigated for treatment of HIV-1. This listing is a research-grade reference compound supplied as a small solid amount for laboratory in vitro and in vivo studies; it is not intended for clinical use.
- Non-nucleoside reverse transcriptase inhibitor activity.
- Research-grade compound for laboratory use.
- High reported purity: 99.9%.
- Supplied as a 5 mg solid.
- Molecular weight approximately 629.28 g·mol⁻¹; formula C24H17BrCl2FN3O5S.
- Powder storage: -20°C; solution storage guidance available.
- Soluble in DMSO (~62.5 mg/mL); may require sonication.
- Not for human or veterinary use.