Imidazopyridines
![eMolecules 1352305-21-5 | C-Imidazo[1,2-a]pyridin-6-yl-methylamine dihydrochloride | J & W PharmLab, LLC | MFCD20921662 | 220.100 | C8H11Cl2N3 | 96.000 | Cl.Cl.NCc1ccc2nccn2c1 | 5g | 250015497](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502155997.JPG-250.jpg)
eMolecules 1352305-21-5 | C-Imidazo[1,2-a]pyridin-6-yl-methylamine dihydrochloride | J & W PharmLab, LLC | MFCD20921662 | 220.100 | C8H11Cl2N3 | 96.000 | Cl.Cl.NCc1ccc2nccn2c1 | 5g | 250015497
C-Imidazo[1,2-a]pyridin-6-yl-methylamine dihydrochloride | J & W PharmLab, LLC | 1352305-21-5 | MFCD20921662 | 220.100 | C8H11Cl2N3 | 96.000 | Cl.Cl.NCc1ccc2nccn2c1 | 5g | 250015497
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.
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
![eMolecules 66358-23-4 | Imidazo[1,2-a]pyridin-5-amine | AA Blocks LLC | MFCD05863377 | 133.154 | C7H7N3 | 0.000 | Nc1cccc2nccn12 | 1g | 410201223](https://assets.fishersci.com/TFS-Assets/CCG/product-images/NC3966728.jpg-250.jpg)
eMolecules 66358-23-4 | Imidazo[1,2-a]pyridin-5-amine | AA Blocks LLC | MFCD05863377 | 133.154 | C7H7N3 | 0.000 | Nc1cccc2nccn12 | 1g | 410201223
Imidazo[1,2-a]pyridin-5-amine | AA Blocks LLC | 66358-23-4 | MFCD05863377 | 133.154 | C7H7N3 | 0.000 | Nc1cccc2nccn12 | 1g | 410201223
![eMolecules 872362-98-6 | (8-Methyl-imidazo[1,2-a]pyridin-2-yl)-methanol | J & W PharmLab LLC | MFCD08752621 | 162.192 | C9H10N2O | 96.000 | Cc1cccn2cc(CO)nc12 | 25g | 452545803](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502155612.JPG-250.jpg)
eMolecules 872362-98-6 | (8-Methyl-imidazo[1,2-a]pyridin-2-yl)-methanol | J & W PharmLab LLC | MFCD08752621 | 162.192 | C9H10N2O | 96.000 | Cc1cccn2cc(CO)nc12 | 25g | 452545803
(8-Methyl-imidazo[1,2-a]pyridin-2-yl)-methanol | J & W PharmLab LLC | 872362-98-6 | MFCD08752621 | 162.192 | C9H10N2O | 96.000 | Cc1cccn2cc(CO)nc12 | 25g | 452545803
![eMolecules 1265896-03-4 | imidazo[1,2-a]pyrazine-3-carboxylic acid | MFCD18432870 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502157410.JPG-250.jpg)
eMolecules 1265896-03-4 | imidazo[1,2-a]pyrazine-3-carboxylic acid | MFCD18432870 | 1g
AstaTech | ()-SECOISOLARICIRESINOL | 1mg | 718346926 | E87134 | 95.000 | 145265-02-7 | 362.422 | C20H26O6
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(F)(F)(F)F.CN1CC[N+](C)=C1N=[N+]=[N-] | 5g | 571814895](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000567248.jpg-250.jpg)
eMolecules 1266134-54-6 | 2-AZIDO-1,3-DIMETHYLIMIDAZOLINIUM HEXAFLUOROPHOSPHATE | AstaTech | MFCD18782891 | 285.134 | C5H10F6N5P | 95.000 | F[P-](F)(F)(F)(F)F.CN1CC[N+](C)=C1N=[N+]=[N-] | 5g | 571814895
2-AZIDO-1,3-DIMETHYLIMIDAZOLINIUM HEXAFLUOROPHOSPHATE | AstaTech | 1266134-54-6 | MFCD18782891 | 285.134 | C5H10F6N5P | 95.000 | F[P-](F)(F)(F)(F)F.CN1CC[N+](C)=C1N=[N+]=[N-] | 5g | 571814895
Medchemexpress LLC Samatasvir | 1312547-19-5 | 99.4% | 885.06 | 5 MG
Samatasvir is a potent, orally active NS5A inhibitor of HCV replication. It is effective and selective against infectious HCV and replicons, with EC50s ranging from 2 to 24 pM in genotype 1 through 5 replicons.
- Potent, orally active NS5A inhibitor of HCV replication.
- Effective and selective against infectious HCV and replicons.
- Retains full activity in the presence of HIV and hepatitis B virus (HBV) antivirals.
- Not cross-resistant with HCV protease, nucleotide, and nonnucleoside polymerase inhibitor classes.
![eMolecules 1332529-24-4 | (2-Imidazo[2,1-b][1,3]thiazol-6-yl-1-methylethyl)amine dihydrochloride | Combi-Blocks | MFCD18071257 | 254.170 | C8H13Cl2N3S | 95.000 | Cl.Cl.CC(N)Cc1cn2ccsc2n1 | 10g | 401041668](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502193012.JPG-250.jpg)
eMolecules 1332529-24-4 | (2-Imidazo[2,1-b][1,3]thiazol-6-yl-1-methylethyl)amine dihydrochloride | Combi-Blocks | MFCD18071257 | 254.170 | C8H13Cl2N3S | 95.000 | Cl.Cl.CC(N)Cc1cn2ccsc2n1 | 10g | 401041668
(2-Imidazo[2,1-b][1,3]thiazol-6-yl-1-methylethyl)amine dihydrochloride | Combi-Blocks | 1332529-24-4 | MFCD18071257 | 254.170 | C8H13Cl2N3S | 95.000 | Cl.Cl.CC(N)Cc1cn2ccsc2n1 | 10g | 401041668