Carboximidamides
Medchemexpress LLC Smap-2 (DT-1154) | 1809068-70-9 | 99.5% | 5 MG
SMAP-2 (DT-1154) is a small-molecule, orally active activator of protein phosphatase 2A (PP2A) with demonstrated anti-cancer activity in preclinical studies. It is supplied as a white to off-white solid and includes manufacturer-reported solubility and storage guidance.
- Orally bioavailable PP2A activator with anticancer activity.
- High purity: 99.53% (manufacturer reported).
- Molecular weight 532.57; formula C27H27F3N2O4S.
- Soluble in DMSO (300 mg/mL); in vivo formulation guidance provided.
- Powder storage: -20°C (3 years) or 4°C (2 years); in solvent: -80°C (2 years).
Medchemexpress LLC β-cryptoxanthin ((3R)-β-cryptoxanthin) | 472-70-8 | MFCD09763658 | ≥99.0% | 552.9 g/mol | C40H56O | 1 MG
β-Cryptoxanthin is an oxygenated carotenoid (C40H56O) found in citrus fruits, red peppers, and pumpkin. It exhibits potent antioxidant activity and reported anti-stress effects, and is provided as a research-grade reagent for studies of antioxidant function, carotenoid metabolism, and nutritional biochemistry.
- Oxygenated carotenoid with antioxidant activity.
- Isolated from fruits and vegetables such as tangerines, red peppers, and pumpkin.
- Used in antioxidant assays and carotenoid biology studies.
- Available in small milligram pack sizes for research use.
- Molecular weight 552.9 g/mol; chemical formula C40H56O.
Medchemexpress LLC Fluorizoline 10mg | 1362243-70-6 | 10 MG
Fluorizoline is a small-molecule research compound that induces apoptosis by selectively binding prohibitin proteins (PHB1 and PHB2) and upregulating pro-apoptotic factors such as NOXA and BIM. It is supplied as a high-purity solid and as a DMSO solution for use in in vitro cellular and biochemical studies.
- Induces apoptosis via prohibitin 1 and 2 binding.
- High purity (99.77%).
- Available in small solid quantities and as a 10 mM DMSO solution.
- White to off-white solid appearance for easy identification.
- Stable when stored under recommended conditions.
eMolecules 134865-70-6 | Medchem Express | 8-M-PDOT | 5mg | 752822498 | HY-101358 | MFCD00901636 | 233.311 | C14H19NO2
ChemScene | (S)-1-(m-Tolyl)ethanamine hydrochloride | 100mg | 632322474 | CS-0153235 | 1630984-18-7 | MFCD11101252 | 171.670 | C9H14ClN
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eMolecules 1321546-70-6 | Medchem Express | (S)-(-)-5-Fluorowillardiine (hydrochloride) | 10mg | 446267739 | HY-16713A | MFCD28385871 | 253.61 | C7H9ClFN3O4
Medchem Express | Chitinase-IN-1 | 5mg | 446269099 | HY-18598 | 1579991-61-9 | MFCD28385840 | 352.410 | C18H16N4O2S
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Medchemexpress LLC 1-tert-butyl N-(5R)-substituted triazole-4-carboxamide (BIIB091) | 2247614-80-6 | 99.9% | 542.64 g/mol | C28H34N10O2 | 5 MG
BIIB091 is a potent, selective, orally active, reversible Bruton tyrosine kinase (BTK) inhibitor supplied for laboratory research. It shows sub-nanomolar enzymatic potency and is provided as solid material or as a DMSO solution for in vitro and preclinical studies; refer to the manufacturer datasheet for safety, handling, and the certificate of analysis.
- Sub-nanomolar BTK potency (IC50 <0.5 nM).
- Reversible and highly selective BTK inhibition.
- Chemical formula C28H34N10O2; molecular weight 542.64 g/mol.
- Available as solid quantities and as a 10 mM solution in DMSO.
- High purity (>99.8% by HPLC) suitable for research applications.
eMolecules 50-01-1 | Guanidine hydrochloride | Chem-Impex | MFCD00013026 | 95.530 | CH6ClN3 | 99.000 | Cl.NC(N)=N | 250g | 322126115
Guanidine hydrochloride | Chem-Impex | 50-01-1 | MFCD00013026 | 95.530 | CH6ClN3 | 99.000 | Cl.NC(N)=N | 250g | 322126115
eMolecules 996-70-3 | TETRAKIS(DIMETHYLAMINO)ETHYLENE | AstaTech | MFCD00009601 | 200.330 | C10H24N4 | 95.000 | CN(C)C(N(C)C)=C(N(C)C)N(C)C | 0.25g | 718059648
TETRAKIS(DIMETHYLAMINO)ETHYLENE | AstaTech | 996-70-3 | MFCD00009601 | 200.330 | C10H24N4 | 95.000 | CN(C)C(N(C)C)=C(N(C)C)N(C)C | 0.25g | 718059648
![eMolecules 479028-70-1 | ChemScene | 4-Fluorobenzo[d]thiazole-2-carboxylic acid | 250mg | 536788692 | CS-0042879 | MFCD11217267 | 197.18 | C8H4FNO2S](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502445391.PNG-250.jpg)
eMolecules 479028-70-1 | ChemScene | 4-Fluorobenzo[d]thiazole-2-carboxylic acid | 250mg | 536788692 | CS-0042879 | MFCD11217267 | 197.18 | C8H4FNO2S
Ambeed | (S)-4-Cyclohexyl-2-(6-(dicyclopentylmethyl)pyridin-2-yl)-45-dihydrooxazole | 100mg | 722704400 | A1519863 | | 380.576 | C25H36N2O
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Medchemexpress LLC Ser-(2,3-Bispalmitoyloxypropyl)-Cys-Gly-Asp-Pro-Lys-His-Pro-Lys-Ser-Phe | 322455-70-9 | 99.2% | 1666.16 | 1 MG
FSL-1 is a bacterial-derived toll-like receptor 2/6 (TLR2/6) agonist that enhances resistance to experimental HSV-2 infection. It significantly reduces HSV-2 replication in vitro and in human vaginal epithelial cells, and induces resistance to experimental genital HSV-2 infection via a specific cytokine response. FSL-1 also enhances phagocytosis of bacteria by macrophages through a Toll-like receptor 2-mediated signaling pathway.
- Enhances resistance to experimental HSV-2 infection.
- Reduces HSV-2 replication in vitro and in human vaginal epithelial cells.
- Induces resistance to genital HSV-2 infection through specific cytokine response.
- Enhances phagocytosis of bacteria by macrophages.
- Functions as a TLR2/6 agonist.
Apexbio Technology LLC Guanidine HCl 50-01-1 10mM (in 1mL H2O)
Guanidine hydrochloride (Guanidine HCl CAS 50-01-1) is a highly alkaline crystalline compound derived from the oxidative metabolism of guanine Functioning primarily as a strong chaotropic agent it disrupts hydrogen bonding and secondary structure in proteins leading to efficient protein denaturation and solubilization Widely utilized in molecular biology and biochemistry Guanidine HCl facilitates protein unfolding for downstream applications such as protein purification refolding studies and RNA extraction protocols where it also serves to inactivate nucleases and other enzymes
Selleck Chemical LLC Allantoin S3856-25mg
Allantoin (Glyoxyldiureide 5-Ureidohydantoin) produced from uric acid is a major metabolic intermediate in most organisms including animals plants and bacteria
Medchemexpress LLC PIN1 inhibitor API-1 25mg | 680622-70-2 | 366.30 g/mol | C15H13F3N6O2 | 25 MG
PIN1 inhibitor API-1 is a small-molecule research compound that inhibits Pin1 (peptidyl-prolyl cis-trans isomerase NIMA-interacting 1) and functions as a microRNA activator. Supplied as a solid with high reported purity, it is suitable for in vitro biochemical and cell-based studies and is soluble in DMSO and in certain co-solvent formulations.