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Filtered Search Results
![eMolecules Medchem Express / (SRS)-AHPC-PEG3-NH2 (hydrochloride) / 10mg / 475641365 / HY-103602 / / 2097971-11-2 / [null] / 656.240 / C30H46ClN5O7S](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502452016.PNG-250.jpg)
eMolecules Medchem Express / (SRS)-AHPC-PEG3-NH2 (hydrochloride) / 10mg / 475641365 / HY-103602 / / 2097971-11-2 / [null] / 656.240 / C30H46ClN5O7S
Medchem Express / (SRS)-AHPC-PEG3-NH2 (hydrochloride) / 10mg / 475641365 / HY-103602 / / 2097971-11-2 / [null] / 656.240 / C30H46ClN5O7S
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Medchemexpress LLC Mal-C6-α-amanitin | 1578249-76-9 | 98.5% | 1211.34 | C55H78N12O17S | 2 MG
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Mal-C6-α-amanitin is an antibody-drug conjugate (ADC) payload consisting of α-amanitin covalently linked via a maleimide C6 (Mal-C6) linker. It is supplied as a solid for research use and acts as an RNA polymerase II inhibitor to provide targeted cytotoxicity.
- Drug-linker conjugate for ADC research and payload development.
- High purity: 98.5%.
- Molecular weight 1211.34 Da.
- Molecular formula C55H78N12O17S.
- White to light yellow solid appearance.
- Store at -20°C; in solvent, store at -80°C up to 6 months (protect from light).
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Medchemexpress LLC 1,2,4-trideoxy-4-(methylamino)-1-(4-pentylphenyl)-D-erythro-pent-1-enitol hydrochloride | 1072443-89-0 | >=98.0% | 313.86 g/mol | C17H27NO2.HCl | 10 MG
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SK1-I is a sphingosine analog and a selective, competitive inhibitor of sphingosine kinase 1 (SPHK1) with a reported Ki of approximately 10 μM. It is supplied for research use and is used in biochemical and cell-based studies to modulate sphingolipid signaling, enhance autophagy, and evaluate antitumor activity.
- Selective SPHK1 inhibitor (Ki ≈ 10 μM).
- Sphingosine analog used in biochemical and cellular assays.
- Reported to enhance autophagy and show antitumor effects in preclinical studies.
- Supplied in small milligram quantities for research use only.
- Common applications include pathway modulation, proliferation, and apoptosis studies.
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Medchemexpress LLC HY-100972 1mg Medchemexpress, ARV-771 CAS:1949837-12-0 Purity:>98%
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Medchemexpress, HY-100972 1mg ARV-771 CAS:1949837-12-0 ARV-771 is a potent BET degrader based on PROTAC technology with Kds of 34 nM, 4.7 nM, 8.3 nM, 7.6 nM, 9.6 nM, and 7.6 nM for BRD2(1), BRD2(2), BRD3(1), BRD3(2), BRD4(1), and BRD4(2), 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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Medchemexpress LLC SM-164 | 957135-43-2 | MFCD28167763 | 5 mg
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SM-164 | Purity: 98.42% | Mol Wt: 1121.42 | 957135-43-2 | MFCD28167763 | 5 mg
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Medchemexpress LLC Neuraminidase-IN-1 | 2379438-80-7 | 98.9% | 317.25 | 50 MG
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Neuraminidase-IN-1 is a neuraminidase inhibitor with an IC50 of 0.21 μM. It exhibits excellent activity against the H1N1 influenza virus.
- Neuraminidase inhibitor
- Excellent activity against H1N1 influenza virus
- Good inhibitory effect on A/WSN/33H1N1 virus strains
- Low toxicity and good druggability
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Medchemexpress LLC HY-13534A 5mg Medchemexpress, Abarelix (Acetate) CAS: Purity:>98%
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Medchemexpress, HY-13534A 5mg Abarelix (Acetate) CAS: Abarelix Acetate (PPI 149 Acetate; R 3827 Acetate) is a potent gonadotrophin-releasing hormone (GnRH) antagonist, used for prostate cancer research. 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 Vh-298 10Mg | HY-100947-10MG
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Vh-298 10Mg
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![eMolecules Medchem Express / (SRS)-AHPC-propargyl / 10mg / 495800262 / HY-126456 / / 2098799-78-9 / [null] / 526.650 / C27H34N4O5S](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502460062.PNG-250.jpg)
eMolecules Medchem Express / (SRS)-AHPC-propargyl / 10mg / 495800262 / HY-126456 / / 2098799-78-9 / [null] / 526.650 / C27H34N4O5S
Medchem Express / (SRS)-AHPC-propargyl / 10mg / 495800262 / HY-126456 / / 2098799-78-9 / [null] / 526.650 / C27H34N4O5S
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Medchemexpress LLC Terlipressin diacetate | 1884420-36-3 | 99.8% | 1347.48 | C56H82N16O19S2 | 25MG
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Terlipressin diacetate is a synthetic vasopressin V1 receptor agonist provided as a high-purity solid peptide for laboratory research. It is typically used to investigate vasoconstriction, portal pressure modulation, and related pharmacological effects. The product includes storage and stability guidance for both powder and solution forms.
- High purity (99.76%) suitable for research use.
- Molecular weight 1347.48 and defined molecular formula.
- Available in multiple pack sizes from 5 mg to 500 mg.
- Storage conditions and stability provided for powder and in-solution forms.
- Supplied as a solid peptide salt appropriate for pharmacology studies.
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![eMolecules Medchem Express / MV1 / 5mg / 459606864 / HY-113534 / / 1001600-54-9 / [null] / 576.738 / C33H44N4O5](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502468537.JPG-250.jpg)
eMolecules Medchem Express / MV1 / 5mg / 459606864 / HY-113534 / / 1001600-54-9 / [null] / 576.738 / C33H44N4O5
Medchem Express / MV1 / 5mg / 459606864 / HY-113534 / / 1001600-54-9 / [null] / 576.738 / C33H44N4O5
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Innovative Research Inc Hmn PAI1 Rcmb WT Act 500ug
Human PAI-1 Recombinant Wild Type Active 500 ug - Human PAI-1 Recombinant Wild Type Active from Innovative Research has been recombinantly produced in E. coli and purified by affinity chromatography. This is a Frozen liquid buffered in 0.05M Sodium Phosphate; 0.1M NaCl; 1mM EDTA; pH 6.6 and a purity of >95% as determined by SDS-PAGE. More Details Species Human Target PAI-1 Purification Method Affinity purified Purity >95% as determined by SDS-PAGE Analysis Source E. coli Storage Conditions -70C Additional Information Gentle purification conditions create an active fraction that is greater than 99% pure and 98% active. This product can be used as a control in applications like ELISA and Western Blot. It can be used in a wide range of in vitro applications, including blocking/inhibition, fibrinolysis, plasminogen activation, receptor binding, in hypertension studies, for protein-protein interactions, and more.
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Medchemexpress LLC Protac BRD4 degrader-9 | 2417370-42-2 | 98.2% | 1312.50 g/mol | C59H71F2N9O15S4 | 1 MG
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PROTAC BRD4 Degrader-9 is a proteolysis-targeting chimera (PROTAC) that induces selective degradation of BRD4 in cellular assays. Supplied as a solid research compound for in vitro use only; not for human or clinical use.
- Targets BRD4 in cellular assays
- Cas number: 2417370-42-2
- Molecular formula: C59H71F2N9O15S4
- Molecular weight: 1312.50 g/mol
- Purity: 98.2%
- Storage: powder at -20°C; in solvent: -80°C for 6 months, -20°C for 1 month
- Available in mg-scale quantities suitable for research use
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Medchemexpress LLC HY-15298A 10mg Medchemexpress, Grazoprevir potassium salt CAS:1206524-86-8 Purity:>98%
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Medchemexpress, HY-15298A 10mg Grazoprevir potassium salt CAS:1206524-86-8 Grazoprevir potassium salt (MK-5172 potassium salt) is a selective inhibitor of Hepatitis C virus NS3/4a protease with broad activity across genotypes and resistant variants, with Kis of 0.01 nM (gt1b), 0.01 nM (gt1a), 0.08 nM (gt2a), 0.15 nM (gt2b), 0.90 nM (gt3a), 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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Medchemexpress LLC HY-10235 100mg , Telaprevir VX-950 CAS:402957-28-2 Purity:98%
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Medchemexpress, HY-10235 100mg Telaprevir VX-950 CAS:402957-28-2 Formula:C36H53N7O6 Ki: 7 nM (genotype 1 HCV NS3-4A protease) Purity:98% Telaprevir is a highly selective, reversible, and potent peptidomimetic inhibitor of the HCV NS3-4A protease , the steady-state inhibitory constant ( K i ) of Telaprevir is 7 nM against a genotype 1 (H strain) NS3 protease domain plus a NS4A cofactor peptide. 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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