Bioactive Small Molecules
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Filtered Search Results
Selleck Chemical LLC Pexidartinib Hydrochloride E6007-1G
Pexidartinib Hydrochloride is an oral tyrosine kinase inhibitor of colony-stimulating factor 1 receptor (CSF1R) It significantly reduces macrophage levels in adipose tissue without altering overall myeloid cell counts in mice It also induces developmental and immunotoxic effects in zebrafish embryos by hyperactivating Wnt signaling
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TARGETMOL CHEMICALS INC BMS-794833 10MG
Also available in 1 mg 2 mg 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. BMS-794833 is a potent ATP competitive inhibitor of Met/VEGFR2; a prodrug of BMS-817378. purity: 99%
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TARGETMOL CHEMICALS INC YNT-185 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. YNT-185 is a nonpeptide selective agonist of the orexin type-2 receptor (OX2R) demonstrating EC50 values of 0.028 uM and 2.75 uM for OX2R and OX1R respectively. Furthermore YNT-185 effectively alleviates symptoms of narcolepsy-cataplexy in mouse models. purity: 98%
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eMolecules 788146-37-2 | SY-21 NHS ester | Broadpharm815.340 | C45H39ClN4O7S | 0.000 | [Cl-].O=C(ON1C(=O)CCC1=O)C1CCN(CC1)S(=O)(=O)c1ccccc1-c1c2ccc(cc2oc2c\c(ccc12)=[N+]1/CCc2ccccc12)N1CCc2ccccc12 | 5mg | 713699975
SY-21 NHS ester | Broadpharm | 788146-37-2815.340 | C45H39ClN4O7S | 0.000 | [Cl-].O=C(ON1C(=O)CCC1=O)C1CCN(CC1)S(=O)(=O)c1ccccc1-c1c2ccc(cc2oc2c\c(ccc12)=[N+]1/CCc2ccccc12)N1CCc2ccccc12 | 5mg | 713699975
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Medchemexpress LLC (S)-XY-05 | 3024030-10-9 | 99.8% | 447.41 g·mol⁻¹ | C20H20F3N7O2 | 10 MG
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PARP7-IN-17 is a potent small-molecule inhibitor of PARP7 with an IC50 of 4.5 nM. It demonstrates oral bioavailability and reported antitumor activity. Supplied as a white to off-white solid for research use, it is commonly used in cellular and in vivo studies of PARP7 biology and anticancer mechanisms.
- Potent PARP7 inhibition (IC50 4.5 nM).
- Reported oral bioavailability and antitumor activity.
- High purity (≈99.8%) suitable for research applications.
- Solid, white to off-white appearance for ease of handling.
- Recommended storage: powder -20°C (up to 3 years) or 4°C (up to 2 years).
- Available in small milligram pack sizes for preclinical studies.
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Medchemexpress LLC Simufilam (PTI-125) | 1224591-33-6 | 99.8% | 259.35 | 1 ML
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Simufilam (PTI-125) is an orally active FLNA modulator. It restores NMDAR signaling and Arc expression, inhibits overactive mTOR signaling by restoring the normal conformation of FLNA, improves insulin sensitivity, and reduces Aβ42-induced neuroinflammation and tau protein hyperphosphorylation. This modulator can be used for research of Alzheimer's disease.
- Restores NMDAR signaling and Arc expression
- Inhibits overactive mTOR signaling
- Improves insulin sensitivity
- Reduces Aβ42-induced neuroinflammation
- Reduces tau protein hyperphosphorylation
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Medchemexpress LLC 5'-O-TBDMS-Bz-dA | 51549-39-4 | 98.37% | 469.61 | 1 ML
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5'-O-TBDMS-Bz-dA is a nucleoside that acts as a protective and modification agent. This white to off-white solid is for research purposes only, not for human use.
- Protective and modification effects
- Used in DNA/RNA synthesis research
- Classified as a nucleoside analog and adenosine derivative
- Related to cancer, blood, and cardio-cerebrovascular disease research
- Soluble in DMSO: 100 mg/mL
- Formulatable for in vivo experiments
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eMolecules 41797-88-0 | ChemScene | 233-Trimethyl-3H-indol-5-ol | 100mg | 768994307 | CS-0617004 | 175.231 | C11H13NO
Medchem Express | Osilodrostat | 2mg | 446267317 | HY-16276 | 928134-65-0 | MFCD25976825 | 227.242 | C13H10FN3
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link:
eMolecules Building Block Tool
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Cayman Chemical CVT-12012, Purity: ≥98%, CAS: 1018675-35-8, 25 mg
An SCD inhibitor (IC50 = 6.1 nM in HepG2 cells); dose-dependently reduces levels of palmitoleic acid and vaccenic acid in the plasma and liver of rats fed a high-sucrose diet; reduces hepatic triglyceride levels in sucrose-fed rats at 20 mg/kg
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Medchemexpress LLC Cxcr2 antagonist 8 | 182498-30-2 | 98.38% | 303.27 | 5 MG
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CXCR2 antagonist 8 is a potent and selective CXCR2 antagonist. It can be used for insulin resistance research.
- Potent and selective CXCR2 antagonist
- Used for insulin resistance research
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Medchemexpress LLC Atg7-IN-2 | 2226227-75-2 | 99.3% | 376.35 | 50 MG
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ATG7-IN-2 (compound 1) is a potent ATG7 inhibitor, with an IC50 of 0.089 μM. It inhibits the autophagy marker LC3B. This product is for research use only and is not sold to patients.
- Potent ATG7 inhibitor with an IC50 of 0.089 μM.
- Inhibits autophagy marker LC3B.
- Inhibits the formation of the ATG7-ATG8 thioester in HEK293 cells with an IC50 of 0.335 μM.
- Suppresses LC3B lipidation in H4 cells with an IC50 of 2.6 μM.
- Reduces cell viability in H1650 cells with an EC50 of 2.6 μM.
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Cayman Chemical 3,4-trimethylene-α-Piperidinovalerophenone (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 Stearoyl glutamic acid sodium | 38517-23-6 | C23H42NNaO5 | 500 MG
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Stearoyl glutamic acid sodium, also known as Sodium stearoyl glutamate, is an anionic emulsifier suitable for cosmetic applications. It also functions as an anionic surfactant and an amino acid alkyl amide sensitizer, which may potentially lead to allergic contact dermatitis.
- Anionic emulsifier for cosmetics.
- Functions as an anionic surfactant.
- An amino acid alkyl amide sensitizer.
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Cayman Chemical Rosavin, Purity: ≥98%, CAS: 84954-92-7, 5 mg
A diglycoside with diverse biological activities; scavenges DPPH radicals in a cell-free assay (IC50 = 5.86 µg/ml); inhibits the proliferation of NCI H69, NCI H526, and NCI H446 SCLC cells at 5-100 µM; inhibits concanavalin A- or anti-CD3 and anti-CD28 antibody-induced growth of Jurkat T cells (IC50s = 80 and 74 µM, respectively) and reduces TRAIL levels in isolated mouse splenic T cells at 0.5, 5, and 50 µM; reduces ferroptosis-related mitochondrial changes and increased levels of 4-HNE and MDA in type II alveolar epithelial cells, as well as reduces lung tissue iron levels, in a rat model of intratracheal PM2.5-induced lung injury at 100 µM
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Medchemexpress LLC GPR84 antagonist 2 | 2244269-74-5 | 99.06% | C28H16Cl2NaO4PS2 | 1 ML
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GPR84 antagonist 2 (compound 33) is a potent, selective, and orally active GPR84 antagonist (IC50=8.95 nM). It demonstrates improved potency in calcium mobilization assays and inhibits neutrophil and macrophage chemotaxis upon GPR84 activation, showing potential for ulcerative colitis research.
- Potent and selective GPR84 antagonist
- Orally active with an IC50 of 8.95 nM
- Improves potency in calcium mobilization assays
- Inhibits neutrophil and macrophage chemotaxis
- Potential for ulcerative colitis research
- Solid storage: -20°C, sealed, away from moisture
- In solvent storage: -80°C for 6 months; -20°C for 1 month, sealed, away from moisture
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