Bioactive Small Molecules
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Filtered Search Results
Cayman Chemical 2-methyl-α-Pyrrolidinoisohexanophenone (hydrochloride), Purity: ≥98%, 5 mg
An analytical reference standard categorized as a cathinone; intended for research and forensic applications
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Medchemexpress LLC HY-17587 500mg Medchemexpress, 4-Methylbenzylidene camphor CAS:36861-47-9 Purity:>98%
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Medchemexpress, HY-17587 500mg 4-Methylbenzylidene camphor CAS:36861-47-9 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-14967 5mg Medchemexpress, NSC 66811 CAS:6964-62-1 Purity:>98%
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Medchemexpress, HY-14967 5mg NSC 66811 CAS:6964-62-1 NSC 66811 is a MDM2-p53 inhibitor, with a Ki of 120 nM for binding to MDM2. 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-131341 5mg Medchemexpress, Syk-IN-4 CAS: Purity:>98%
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Medchemexpress, HY-131341 5mg Syk-IN-4 CAS: Syk-IN-4 is a potent, selective and orally bioavailable SYK inhibitor with an IC50 of 0.31 nM. SYK has emerged as a potential target for autoimmunity and hematological cancers. 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-134334 5mg Medchemexpress, C/EBPα inducer 1 CAS:2374285-52-4 Purity:>98%
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Medchemexpress, HY-134334 5mg C/EBPα inducer 1 CAS:2374285-52-4 C/EBPα inducer 1 (compound 78) is a potent inducer of C/EBPα and myeloid differentiation. 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-133083 5mg Medchemexpress, BAY-474 CAS:1033767-86-0 Purity:>98%
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Medchemexpress, HY-133083 5mg BAY-474 CAS:1033767-86-0 BAY-474 is a tyrosine-protein kinase c-Met inhibitor. BAY-474 acts as an epigenetics probe. 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 TP-021 (BCL6-IN-8c) | 2130878-25-8 | 99.1% | 25 MG
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TP-021 (BCL6-IN-8c) is a chemical probe that inhibits the interaction between B-cell lymphoma 6 (BCL6) and its corepressors. It is a potent, orally active inhibitor with an IC50 of 0.10 μM, supplied as a 25 mg solid for research use.
- Potent BCL6-corepressor interaction inhibitor with IC50 0.10 μM.
- High purity, supporting biochemical and cellular studies.
- Soluble in DMSO at ≥ 50 mg/mL.
- Powder stable at -20°C for long-term storage; solvent stability varies.
- Supplied as a 25 mg solid for laboratory research.
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Cayman Chemical JNJ-26481585 (hydrochloride), Purity: ≥98%, CAS: 875320-31-3, 1 mg
A pan-HDAC inhibitor; inhibits class I (IC50s = 0.11-4.86 nM for HDAC1-3 and HDAC8, respectively), inhibits class IIa (IC50s = 0.64-119 nM for HDAC4-5 and HDAC7-9), and class IIb HDACs (IC50s = 76.8 and 0.46 nM for HDAC6 and HDAC10, respectively), as well as the class IV HDAC HDAC11 (IC50 = 0.37 nM); induces apoptosis, pyroptosis, and ferroptosis in CAL-27 and Tca8113 cells at 200 nM; completely inhibits tumor growth in HCT116 Ras mutant and C170HM2 mouse xenograft models at 10 mg/kg once per day
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Cayman Chemical Tegobuvir, Purity: ≥98%, CAS: 1000787-75-6, 1 mg
A non-nucleoside inhibitor of HCV NS5B; reduces viral infectivity in cells expressing wild-type HCV 1b NS5B but not mutant NS5Bs; selectively inhibits replication of HCV genotypes 1a and 1b over genotype 2a in Huh7-Lunet cells (EC50s = 13.8, 0.8, and 21,900 nM, respectively)
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TARGETMOL CHEMICALS INC ABETA-IN-1 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. A(beta)-IN-1 is a novel potent and orally active (gamma)-secretase modulator (GSM). A(beta)-IN-1 potently reduced A(beta)42 levels with an IC 50 value of 0.091 uM in cultured cells without inhibiting CYP3A4. A(beta)-IN-1 shows a sustained pharmacokinetic profile. purity: 98%
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TARGETMOL CHEMICALS INC MD2-TLR4-IN-1 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. MD2-TLR4-IN-1 is a myeloid differentiation protein 2/toll-like receptor 4 (MD2-TLR4) complex inhibitor. purity: 99%
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Medchemexpress LLC HY-130684 5mg Medchemexpress, MDM2-IN-1 CAS:1410737-09-5 Purity:>98%
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Medchemexpress, HY-130684 5mg MDM2-IN-1 CAS:1410737-09-5 MDM2-IN-1 (Compound 30) is a synthetic MDM2-p53 interaction (MDM2) inhibitor and contains the trans (D-)configuration. 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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Cayman Chemical 6-Methylmercaptopurine-d3, Purity: ≥99% deuterated forms (d1-d3), CAS: 33312-93-5, 5 mg
An internal standard for the quantification of 6-MMP by GC- or LC-MS
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Medchemexpress LLC DfTat | 2035480-78-3 | 99.5% | 4076.83 | 5 MG
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DfTat is a dimer of the prototypical cell-penetrating peptide TAT. It can efficiently deliver small molecules, peptides, and proteins into live cells. When labeled with rhodamine, DfTat can be used as a tracer for easy detection.
- Dimer of cell-penetrating peptide TAT
- Delivers small molecules, peptides, and proteins into live cells
- Offers high efficiency for delivery
- Labeled with rhodamine for easy detection
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Medchemexpress LLC Corilagin, a gallotannin | 23094-69-1 | 634.45 | 20 MG
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Corilagin, a gallotannin, exhibits anti-tumor, anti-inflammatory, and hepatoprotective activities. It inhibits the activity of reverse transcriptase of RNA tumor viruses and the growth of *Staphylococcus aureus* (MIC of 25 μg/mL). Corilagin also demonstrates anti-tumor activity in hepatocellular carcinoma and ovarian cancer models, with low toxicity to normal cells and tissues.
- Purity: 99.96%
- Appearance: Solid
- Color: White to off-white
- Structure classification: Phenols, polyphenols
- Initial source: Plants, Euphorbiaceae, Phyllanthus urinaria Linn.
- Solubility in DMSO: 100 mg/mL (requires ultrasonic)
- Exhibits anti-tumor activity
- Exhibits anti-inflammatory activity
- Exhibits hepatoprotective activities
- Inhibits reverse transcriptase of RNA tumor viruses
- Inhibits growth of Staphylococcus aureus
- Shows low toxicity to normal cells and tissues
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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