CSNpharm
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Moroxydine HCl is an antiviral drug used to treat influenza, active against RNA and DNA viruses. It is also an inhibitor of PTP1B and TCPTP inhibitor with IC50 values of 80-160 nM.
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Moroxydine HCl is an antiviral drug used to treat influenza, active against RNA and DNA viruses. It is also an inhibitor of PTP1B and TCPTP inhibitor with IC50 values of 80-160 nM.
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Morroniside is a naturally occuring iridoid which can regulate hair growth and cycle transition via activation of the Wnt/β-catenin signaling pathway.
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Morroniside is a naturally occuring iridoid which can regulate hair growth and cycle transition via activation of the Wnt/β-catenin signaling pathway.
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CSNpharm
Morroniside is a naturally occuring iridoid which can regulate hair growth and cycle transition via activation of the Wnt/β-catenin signaling pathway.
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CSNpharm
Morroniside is a naturally occuring iridoid which can regulate hair growth and cycle transition via activation of the Wnt/β-catenin signaling pathway.
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Morusin shows suppression of NFκB and STAT3 in many cancer cell lines including HT-29, A549, MCF-7, and MDA-MB-231. It is a flavonoid purified from the root bark of morus alba L. with antitumor activity.
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Morusin shows suppression of NFκB and STAT3 in many cancer cell lines including HT-29, A549, MCF-7, and MDA-MB-231. It is a flavonoid purified from the root bark of morus alba L. with antitumor activity.
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Morusin shows suppression of NFκB and STAT3 in many cancer cell lines including HT-29, A549, MCF-7, and MDA-MB-231. It is a flavonoid purified from the root bark of morus alba L. with antitumor activity.
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CSNpharm
Morusin shows suppression of NFκB and STAT3 in many cancer cell lines including HT-29, A549, MCF-7, and MDA-MB-231. It is a flavonoid purified from the root bark of morus alba L. with antitumor activity.
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Morusinol, a natural product isolated and purified from the root bark of Morus alba L., may significantly inhibit arterial thrombosis in vivo due to antiplatelet activity, may exert beneficial effects on transient ischemic attacks or stroke via the modulation of platelet activation.
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CSNpharm
Morusinol, a natural product isolated and purified from the root bark of Morus alba L., may significantly inhibit arterial thrombosis in vivo due to antiplatelet activity, may exert beneficial effects on transient ischemic attacks or stroke via the modulation of platelet activation.
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Moxalactam sodium is an antibiotic compound more effective against Escherichia coli and Pseudomonas aeruginosathan cephalosporins.
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Moxalactam sodium is an antibiotic compound more effective against Escherichia coli and Pseudomonas aeruginosathan cephalosporins.
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Moxifloxacin is a fourth-generation fluoroquinolone antibiotic with expanded activity against gram-positive bacteria as well as atypical pathogens.
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CSNpharm
Moxifloxacin is a fourth-generation fluoroquinolone antibiotic with expanded activity against gram-positive bacteria as well as atypical pathogens.
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Moxonidine is a selective agonist of imidazoline I1 receptors and alpha-2 receptor used as an antihypertensive drug.
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Moxonidine is a selective agonist of imidazoline I1 receptors and alpha-2 receptor used as an antihypertensive drug.
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Moxonidine is a selective agonist of imidazoline I1 receptors and alpha-2 receptor used as an antihypertensive drug.
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CSNpharm
Moxonidine is a selective agonist of imidazoline I1 receptors and alpha-2 receptor used as an antihypertensive drug.
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Mozavaptan is a competitive vasopressin receptor antagonist for both V1 and V2 receptors with IC50 of 1.2 μM and 14 nM, respectively.
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Mozavaptan is a competitive vasopressin receptor antagonist for both V1 and V2 receptors with IC50 of 1.2 μM and 14 nM, respectively.
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CSNpharm
Mozavaptan is a competitive vasopressin receptor antagonist for both V1 and V2 receptors with IC50 of 1.2 μM and 14 nM, respectively.
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CSNpharm
Mozavaptan is a competitive vasopressin receptor antagonist for both V1 and V2 receptors with IC50 of 1.2 μM and 14 nM, respectively.
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MPEP
25mg
| ≥98%
CSNpharm
MPEP is a potent and highly selective non-competitive antagonist at the mGlu5 receptor subtype (IC50 = 36 nM) and a positive allosteric modulator at mGlu4 receptors.
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MPEP
10mg
| ≥98%
CSNpharm
MPEP is a potent and highly selective non-competitive antagonist at the mGlu5 receptor subtype (IC50 = 36 nM) and a positive allosteric modulator at mGlu4 receptors.
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MPEP
50mg
| ≥98%
CSNpharm
MPEP is a potent and highly selective non-competitive antagonist at the mGlu5 receptor subtype (IC50 = 36 nM) and a positive allosteric modulator at mGlu4 receptors.
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CSNpharm
MPEP HCl is a potent and highly selective non-competitive antagonist at the mGlu5 receptor subtype with IC50 of 36 nM.
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CSNpharm
MPEP HCl is a potent and highly selective non-competitive antagonist at the mGlu5 receptor subtype with IC50 of 36 nM.
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CSNpharm
MPEP HCl is a potent and highly selective non-competitive antagonist at the mGlu5 receptor subtype with IC50 of 36 nM.
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