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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences Bafilomycin A1 from Streptomyces griseus | 88899-55-2 | MFCD06795130 | 2 ug
Bafilomycin A1 from Streptomyces griseus | Purity: 90% | Mol Wt: 622.83 | 88899-55-2 | MFCD06795130 | 2 ug
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Sigma Aldrich Fine Chemicals Biosciences 4-Hexylresorcinol analytical standard | 136-77-6 | MFCD00002284 | 25MG
4-Hexylresorcinol analytical standard | Purity: >=98.0% (GC) | Mol Wt: 194.27 | 136-77-6 | MFCD00002284 | 25MG
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Medchemexpress LLC Fenbendazole-d3 | 1228182-47-5 | MFCD16652570 | 99.7% | 302.37 g/mol | C15H10D3N3O2S | 10 MG
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Fenbendazole-d3 is a deuterium-labeled analogue of fenbendazole used as an analytical reference standard and tracer in research. It is applied in pharmacokinetic and metabolism studies and shows microtubule destabilizing and antiparasitic activity, with reported antitumor effects in preclinical models.
- Deuterium-labeled reference standard for analytical studies.
- High purity: 99.7% as supplied.
- Suitable for pharmacokinetic and metabolism tracing.
- Exhibits microtubule destabilizing activity and antiparasitic effects.
- Available in small quantities for laboratory use (e.g., 10 mg).
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC MC-Val-Cit-PAB-Auristatin E | 2055896-77-8 | 97.0% | 1287.65 | C68H108N11O13 | 5 MG
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MC-Val-Cit-PAB-Auristatin E is an antibody-drug conjugate (ADC) linker-payload conjugate for research use. It links the cytotoxic tubulin inhibitor auristatin E to an MC-Val-Cit-PAB cleavable linker, enabling enzymatic release of the payload in target cells. The material is provided as a solid for preclinical and ADC development studies.
- cleavable val-cit dipeptide linker enabling enzymatic payload release
- contains auristatin E tubulin inhibitor as the payload
- molecular formula C68H108N11O13 and molecular weight 1287.65
- purity ~97.0% by HPLC (batch-specific certificate of analysis available)
- supplied as a solid with good solubility in DMSO for formulation
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Sigma Aldrich Fine Chemicals Biosciences Chlortetracycline hydrochloride >=91.0% dry basis (HPLC) | 64-72-2 | MFCD00082440 | 25G
Chlortetracycline hydrochloride >=91.0% dry basis (HPLC) | Purity: >=91.0% dry basis (HPLC) | Mol Wt: 515.34 | 64-72-2 | MFCD00082440 | 25G
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Medchemexpress LLC Thz1 (hydrochloride) | 1604810-83-4 | MFCD28167785 | 99.1% | 602.51 g/mol | C31H29Cl2N7O2 | 10 MG
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THZ1 (hydrochloride) is the hydrochloride salt of THZ1, a selective, covalent inhibitor of cyclin-dependent kinase 7 (CDK7) with low-nanomolar potency. It also inhibits CDK12 and CDK13 and is used in preclinical studies to probe transcriptional regulation, cell-cycle control, and oncology models.
- Selective covalent CDK7 inhibitor (IC50 ~3.2 nM).
- Hydrochloride salt form for improved handling.
- Molecular formula C31H29Cl2N7O2; molecular weight 602.51 g/mol.
- High purity (~99.06%) suitable for research applications.
- Supplied in small research sizes, including 10 MG.
- Certificate of analysis and safety data sheet available.
- Common applications: transcriptional regulation, cell-cycle, and oncology research.
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![Medchemexpress LLC [4-[[5-chloro-4-(methylamino)-7H-pyrrolo[2,3-d]pyrimidin-2-yl]amino]-3-methoxyphenyl]-4-morpholinyl- | 1700693-08-8 | MFCD29472241 | 98.0% | 416.86 g/mol | C19H21ClN6O3 | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000298359.png-250.jpg)
Medchemexpress LLC [4-[[5-chloro-4-(methylamino)-7H-pyrrolo[2,3-d]pyrimidin-2-yl]amino]-3-methoxyphenyl]-4-morpholinyl- | 1700693-08-8 | MFCD29472241 | 98.0% | 416.86 g/mol | C19H21ClN6O3 | 10 MG
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JH-II-127 is an orally active, highly potent, selective, and brain-permeable inhibitor of leucine-rich repeat kinase 2 (LRRK2) used in preclinical research to probe LRRK2 signaling and Parkinson's disease models. It shows low-nanomolar activity against wild-type and mutant LRRK2 and has characterized solubility and storage profiles for in vitro and in vivo studies.
- Highly potent LRRK2 inhibition (low-nanomolar IC50 values).
- Selective activity against wild-type and mutant LRRK2 variants.
- Brain permeable, suitable for central nervous system studies.
- High purity solid with defined storage conditions for stability.
- Documented solubility protocols for in vitro and in vivo use.
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Medchemexpress LLC Chloramphenicol palmitate | 530-43-8 | 98.25% | 25 MG
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Chloramphenicol palmitate is an orally active prodrug of Chloramphenicol, formed by the esterification of the agent with Palmitic acid. It is rapidly and completely hydrolyzed by intestinal esterase, releasing Chloramphenicol, which is an orally effective broad-spectrum antibiotic. For research use only. MedChemExpress (MCE) does not sell to patients.
- Orally active prodrug of Chloramphenicol.
- Rapidly and completely hydrolyzed by intestinal esterase.
- Releases Chloramphenicol, an orally effective broad-spectrum antibiotic.
- In vivo, chloramphenicol palmitate (10% dry formulation; p.o.; four doses) achieves steady-state plasma chloramphenicol concentrations of 5-6 μg/mL in four female beef-type calves, with an elimination half-life of 4.5 hours (chloramphenicol).
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Sigma Aldrich Fine Chemicals Biosciences Streptomycin sulfate salt powder | 3810-74-0 | MFCD00037023 | 25G
Streptomycin sulfate salt powder | Mol Wt: 728.69 | 3810-74-0 | MFCD00037023 | 25G
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Medchemexpress LLC Sodium copper chlorophyllin B | 28302-36-5 | 500 MG
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Sodium copper chlorophyllin B is a compound that demonstrates antiviral activities against Influenza virus and HIV, with IC50s ranging from 50 to 100 μM for both. It is intended for research use only and exhibits inhibition of influenza virus adsorption at 200 μM and HIV adsorption at 2.5 mM.
- Antiviral activity against influenza virus and HIV.
- IC50s of 50 to 100 μM for both influenza virus and HIV.
- Inhibits influenza virus adsorption at 200 μM.
- Inhibits HIV adsorption at 2.5 mM.
- Intended for research use only.
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Santa Cruz Biotechnology Puromycin dihydrochloride | 58-58-2 | MFCD00012691 | 25 mg
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Puromycin dihydrochloride | Purity: ≥98% | Mol Wt: 544.43 | 58-58-2 | MFCD00012691 | 25 mg
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Sigma Aldrich Fine Chemicals Biosciences Mitomycin C from Streptomyces Caespitosus | 50-07-7 | MFCD00078109 | 2mg
Mitomycin C from Streptomyces Caespitosus | Purity: 98% | Mol Wt: 334.33 | 50-07-7 | MFCD00078109 | 2mg ** For R&D use only. Not for drug, household, or other uses.
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Apexbio Technology LLC APEXBIO TECHNOLOGY LLC
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5000570432 CLINDAMYCIN-ALCOHOLATE-1G
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Biolegend PUROMYCIN DIHYDROCHLORIDE
5000125902 PUROMYCIN DIHYDROCHLORIDE
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![Medchemexpress LLC Thioperoxydicarbonic acid ([(HO)C(S)]2S2), OC, OC'-diethyl ester | 502-55-6 | 98.0% | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000412096-logo.png-250.jpg){kind=logo}
Medchemexpress LLC Thioperoxydicarbonic acid ([(HO)C(S)]2S2), OC, OC'-diethyl ester | 502-55-6 | 98.0% | 100 MG
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Dixanthogen is a dimer formed by the oxidation of xanthate. It can indirectly reflect the residual level of xanthates in water bodies. Xanthates are commonly used collectors in flotation processes but are highly toxic to the aquatic environment.
- Dimer formed by oxidation of xanthate
- Can indirectly reflect residual xanthate levels in water
- For research use only
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