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Filtered Search Results
Medchemexpress LLC HY-N0674 5mg Medchemexpress, Dehydrocorydaline CAS:30045-16-0 Purity:>98%
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Medchemexpress, HY-N0674 5mg Dehydrocorydaline CAS:30045-16-0 Dehydrocorydaline (13-Methylpalmatine) is an alkaloid isolated from traditional Chinese herb Corydalis yanhusuo W.T. Wang. Dehydrocorydaline regulates protein expression of Bax , Bcl-2 ; activates caspase-7 , caspase-8 , and inactivates PARP . Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC Amphotericin B methyl ester | 36148-89-7 | MFCD30719782 | 83.4% | 938.11 | C48H75NO17 | 5 MG
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Amphotericin B methyl ester is the methyl ester derivative of the polyene antibiotic Amphotericin B. It is a cholesterol-binding antifungal compound reported to disrupt HIV-1 particle production and inhibit HIV-1 replication. The material is supplied as a solid for research use.
- Methyl ester derivative of Amphotericin B.
- Cholesterol-binding antifungal activity.
- Reported to disrupt HIV-1 particle production and inhibit replication.
- Solid, light yellow to yellow appearance.
- Molecular weight approximately 938.11; formula C48H75NO17.
- Purity approximately 83.4%.
- Store at -20°C and protect from light; in solvent store at -80°C up to 6 months.
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Medchemexpress LLC HY-B2157 100mg Medchemexpress, Robenidine hydrochloride CAS:25875-50-7 Purity:>98%
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Medchemexpress, HY-B2157 100mg Robenidine hydrochloride CAS:25875-50-7 Robenidine hydrochloride is an anticoccidial agent which is also active against MRSA and VRE with MIC 50 s of 8.1 and 4.7 μM, respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Selleck Chemical LLC Tigecycline S1403-200mg
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Tigecycline is bacteriostatic and is a protein synthesis inhibitor by binding to the 30S ribosomal subunit of bacteria and thereby blocking entry of Aminoacyl-tRNA into the A site of the ribosome during prokaryotic translation Tigecycline induces autophagy by downregulating the PI3K-AKT-mTOR pathway
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Selleck Chemical LLC BX-912 S1275-2mg
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BX912 is a potent and specific PDK1 inhibitor with IC50 of 12 nM 9- and 105- fold greater selectivity for PDK1 than PKA and PKC in cell-free assays respectively In comparison to GSK3 selectivity for PDK1 is 600-fold
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Selleck Chemical LLC Chloroquine diphosphate S4157-200mg
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Chloroquine diphosphate is a 4-aminoquinoline anti-malarial and anti-rheumatoid agent also acting as an ATM activator Chloroquine is also an inhibitor of toll-like receptors (TLRs)
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Medchemexpress LLC HY-B2226 1g Medchemexpress, Sodium copper chlorophyllin B CAS:28302-36-5 Purity:>98%
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Medchemexpress, HY-B2226 1g Sodium copper chlorophyllin B CAS:28302-36-5 Sodium copper chlorophyllin B exerts antiviral activities against Influenza virus and HIV with IC 50 s of 50 to 100 μM for both of them. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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VECTOR LABORATORIES LLC BTTAA 100 MG
502387035 BTTAA 100 MG
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MEDCHEMEXPRESS LLC CB 300919 5MG
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501873023 CB 300919 5MG
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MEDCHEMEXPRESS LLC ISAVUCONAZOLE 5MG
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501873017 ISAVUCONAZOLE 5MG
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Medchemexpress LLC HY-12169 10mg Medchemexpress, Marimastat CAS:154039-60-8 Purity:>98%
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Medchemexpress, HY-12169 10mg Marimastat CAS:154039-60-8 Marimastat (BB2516) is a broad spectrum and orally bioavailable inhibitor of MMPs, with potent activity against MMP-9 (IC50=3 nM), MMP-1 (IC50=5 nM), MMP-2 (IC50=6 nM), MMP-14 (IC50=9 nM) and MMP-7 (IC50=13 nM), used in the treatment of cancer. Marimastat (BB2516) is an angiogenesis and metastasis inhibitor, which limits the growth and production of blood vessels. As an antimetatstatic agent it prevents malignant cells from breaching the basement membranes[2]. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-12683 10mg Medchemexpress, BPTES CAS:314045-39-1 Purity:>98%
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Medchemexpress, HY-12683 10mg BPTES CAS:314045-39-1 BPTES is an allosteric and selective glutaminase inhibitor with an IC50 of 0.16 μM. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC SAR405 | 1523406-39-4 | MFCD28411361 | >98.0% | 443.9 | C19H21ClF3N5O2 | 2MG
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SAR405 is a research-grade small-molecule inhibitor of the class III phosphatidylinositol 3-kinase (Vps34/PIK3C3). It potently inhibits Vps34 activity (reported IC50 = 1.2 nM; Kd = 1.5 nM) and is used in cellular and biochemical studies to block autophagosome formation and alter vesicle trafficking. Supplied as a high-purity solid suitable for laboratory research.
- Potent Vps34 inhibitor (IC50 = 1.2 nM).
- Blocks autophagosome formation and inhibits autophagy.
- Useful for cellular and biochemical studies of vesicle trafficking.
- Supplied as a high-purity solid or powder for research use.
- Available in small, research-scale quantities suitable for assay development.
- Characterized in peer-reviewed publications for target engagement.
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Medchemexpress LLC L-homocysteine, S-[2-[(1-iminoethyl)amino]ethyl]-, phosphate (1:1) | 438542-15-5 | 98.0% | 100 MG
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GW274150 phosphate is a potent, selective, orally active NADPH-dependent inhibitor of inducible nitric oxide synthase (iNOS) used in research to probe iNOS-mediated signaling and inflammatory responses (human IC50 = 2.19 μM; Kd = 40 nM).
- Potent iNOS inhibitor with reported human IC50 2.19 μM and Kd 40 nM.
- High reported purity: 98.0% (LCMS).
- Molecular weight 317.30; formula C8H20N3O6PS.
- White to off-white solid; soluble in water and PBS with ultrasonic or heating assistance.
- Storage recommendations: keep dry at 4°C; in solution store -80°C (6 months) or -20°C (1 month).
- For research use only; not for human or clinical use.
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Medchemexpress LLC Retro-2 | 1201652-50-7 | 98.0% | 50 MG
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Retro-2 is a small-molecule inhibitor that selectively blocks retrograde protein trafficking at the endosome-trans-Golgi network interface and shows reported antiviral activity in cellular studies.
- Selective inhibitor of retrograde protein trafficking.
- Reported antiviral activity in cell-based assays.
- Induces autophagy in treated cells.
- High purity (98.0%).
- Solid form; recommended storage at 4°C and protection from light.
- Available in a 50 mg pack size for research use.
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