Bioactive Small Molecules
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Filtered Search Results
Medchemexpress LLC N1,N5-Bis-boc-spermidine | 68076-39-1 | 99.8% | 345.48 | 100 MG
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N1,N5-Bis-Boc-spermidine is a linker that features an amino group along with two Boc-protected amino groups. This amino group is reactive with various substances such as carboxylic acids, activated NHS esters, and carbonyls like ketone and aldehyde. The Boc group can be deprotected when exposed to mild acidic conditions, resulting in the formation of a free amine.
- Linker containing an amino group with two Boc-protected amino groups.
- Amino group is reactive with carboxylic acids, activated NHS esters, and carbonyls (ketone, aldehyde).
- Boc group can be deprotected under mild acidic conditions to form the free amine.
- Soluble in DMSO at a concentration of at least 100 mg/mL (289.45 mM).
- Store at 4°C, protected from light.
- When in solvent, store at -80°C for 6 months or -20°C for 1 month (protect from light).
- Purity is 99.78%.
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Apexbio Technology LLC Sivelestat sodium tetrahydrate, 10mg CAS# 201677-61-4
Sivelestat sodium tetrahydrate is a potent competitive inhibitor of human neutrophil elastase (HNE) with IC50 of 44 nM and Ki of 0.2 M. It is also known as ONO5046, LY544349 and EI546. It can also inhibit leukocyte elastase in rabbit, rat, hamster and mouse. Other sizes are also available. Please inqury us for quote.
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Cayman Chemical MPP-PICA, Purity: ≥98%, 1 mg
An analytical reference standard that is structurally similar to known synthetic cannabinoids; intended for research and forensic applications
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AdipoGen 7-Amino-NBD
Chemical. CAS 10199-91-4. Formula C6H4N4O3. MW 180.12. Synthetic. Fluorogenic amine. Building block and reagent for synthesis of fluorescent probes. Used for the preparation of fluorogenic substrates, chemosensors and probes, in which NBD-amine is the high fluoresence component after release. Shows constant fluorescence intensity from pH2-9. Spectral data Ex=472nm, Em=555nm TRIS buffer, pH7.8
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TARGETMOL CHEMICALS INC PNZ5 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. PNZ5 is a potent and isoxazole-based pan-BET inhibitor with high selectivity and potency similar to the well-established (+)-JQ1 with a KD of 5.43 nM for BRD4(1). purity: 99%
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Cayman Chemical TA-02, Purity: ≥98%, CAS: 1784751-19-4, 10 mg
An inducer of cardiomyocyte differentiation; increases expression of the cardiomyocyte marker NKX2-5 by >2-fold and decreases expression of mesoderm markers and the pre-cardiac marker Isl-1 in HES-3 NKX2-5eGFP/w cells at 5 μM; inhibits CK1ε and CK1D and reduces expression of Wnt/β-catenin signaling pathway members
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Cayman Chemical RAF709, Purity: ≥98%, CAS: 1628838-42-5, 1 mg
A potent inhibitor of B-RAF and C-RAF (IC50s = 0.4 and 0.5 nM, respectively); selective for RAF kinases exhibiting >99% inhibition of only B-RAF, B-RAFV600E, and C-RAF in a panel of 456 kinases; DDR1, DDR2, FRK, and PDGFRβ are also inhibited by >80% at a concentration of 1 μM; inhibits phosphorylation of MEK and ERK (EC50s = 0.02 and 0.1 μM, respectively) with minimal paradoxical activation, stabilizes BRAF-CRAF dimers (EC50 = 0.8 μM), and reduces proliferation of Calu-6 RAS mutant cells (EC50 = 0.95 μM); reduces ERK phosphorylation and decreases tumor volume without affecting total body weight in a Calu-6 mouse NSCLC xenograft model when administered at doses ranging from 10-200 mg/kg
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Medchemexpress LLC KIR2DL1 Human Biot 20ug | 20ug
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KIR2DL1 found on NK cells serves as a receptor for specific HLA-C alleles inhibiting NK cell activity to prevent cell lysis This regulatory function involves interactions with ARRB2 and additionally engages PTPN6 and PTPN11 The interaction s enhancement by ARRB2 underscores KIR2DL1 s role in complex signaling networks that modulate NK cell function KIR2DL1 Protein Human (Biotinylated HEK293 His-Avi) is the recombinant human-derived KIR2DL1 protein expressed by HEK293 with C-Avi C-His labeled tag
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Medchemexpress LLC Amilo-5MER TFA (5-MP TFA) | 99.6% | 576.66 (free base) | 5 MG
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Amilo-5MER TFA (5-MP) is an orally active and selective Serum Amyloid A (SAA) inhibitor. It specifically inhibits the release of pro-inflammatory cytokines IL-6 and IL-1β from SAA-activated cells. This compound has shown the ability to reduce chronic inflammation and alleviate symptoms associated with diseases like rheumatoid arthritis (RA), inflammatory bowel disease (IBD), and multiple sclerosis (MS). It is considered promising for research in autoimmune and chronic inflammatory diseases.
- Orally active and selective Serum Amyloid A (SAA) inhibitor.
- Specifically inhibits the release of pro-inflammatory cytokines IL-6 and IL-1β from SAA-activated cells.
- Reduces chronic inflammation.
- Relieves symptoms of diseases such as rheumatoid arthritis (RA), inflammatory bowel disease (IBD), and multiple sclerosis (MS).
- Promising for research of autoimmune diseases and chronic inflammatory diseases.
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eMolecules 1416881-52-1 | 4CzIPN | ChemScene788.914 | C56H32N6 | 98.000 | N#Cc1c(c(C#N)c(c(c1-n1c2ccccc2c2ccccc12)-n1c2ccccc2c2ccccc12)-n1c2ccccc2c2ccccc12)-n1c2ccccc2c2ccccc12 | 1g | 572189573
4CzIPN | ChemScene | 1416881-52-1788.914 | C56H32N6 | 98.000 | N#Cc1c(c(C#N)c(c(c1-n1c2ccccc2c2ccccc12)-n1c2ccccc2c2ccccc12)-n1c2ccccc2c2ccccc12)-n1c2ccccc2c2ccccc12 | 1g | 572189573
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eMolecules 79756-69-7 | Medchem Express | TPI-1 | 5mg | 446255535 | HY-100463 | MFCD00448731 | 253.08 | C12H6Cl2O2
Medchem Express | TPI-1 | 5mg | 446255535 | HY-100463 | 79756-69-7 | MFCD00448731 | 253.080 | C12H6Cl2O2
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Cayman Chemical Didecanoin, Purity: ≥98%, CAS: 53988-07-1, 250 mg
A diacylglycerol
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Medchemexpress LLC [D-Ala2]leucine-enkephalin | 64963-01-5 | 98.6% | 569.65 | 1 ML
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[D-Ala2]leucine-enkephalin is a delta opioid agonist and a degradation-resistant, long-acting Leu-enkephalin analog. It is used to study the signaling pathway of delta opioid receptors. It is widely distributed in the human body and possesses vital physiological functions.
- Activates dormant brain cells and facilitates recovery of sequelae from brain damage.
- Enhances immune system activity, including T lymphocytes, NK cells, and macrophages.
- Exerts antiviral effects and promotes gamma-interferon secretion.
- Participates in immune regulation by stimulating endocrine cell secretion, influencing gene regulation and DNA expression.
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Cayman Chemical BAY 12-17389, Purity: ≥95%, CAS: 1554458-53-5, 1 mg
An Mps1 inhibitor (IC50 = 0.63 nM); selective for Mps1 over a panel of kinases at 10 nM; promotes mitosis progression in metaphase-arrested HeLa cells (IC50 = 11 nM); enhances paclitaxel-induced inhibition of tumor growth in a SUM149 TNBC mouse xenograft model
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Medchemexpress LLC [D-Leu-4]-OB3 | 289056-32-2 | 98.9% | 734.82 | 5 MG
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[D-Leu-4]-OB3 is an agent that inhibits the expression of pro-inflammatory, proliferative, and metastatic genes, as well as PD-L1 expression. It also stimulates the expression of pro-apoptotic genes.
- Inhibits pro-inflammatory genes
- Inhibits proliferative genes
- Inhibits metastatic genes
- Inhibits PD-L1 expression
- Stimulates pro-apoptotic genes
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