Benzamides
Sigma Aldrich Fine Chemicals Biosciences Aminopterin powder, BioReagent, suitable for cell culture | 54-62-6 | 100MG
Aminopterin powder, BioReagent, suitable for cell culture | Purity: >=97% | Mol Wt: 440.41 | 54-62-6 | 100MG
Sigma Aldrich Fine Chemicals Biosciences Aminopterin powder, BioReagent, suitable for cell culture | 54-62-6 | 25MG
Aminopterin powder, BioReagent, suitable for cell culture | Purity: >=97% | Mol Wt: 440.41 | 54-62-6 | 25MG
Sigma Aldrich Fine Chemicals Biosciences Aminopterin powder, BioReagent, suitable for cell culture | 54-62-6 | 10MG
Aminopterin powder, BioReagent, suitable for cell culture | Purity: >=97% | Mol Wt: 440.41 | 54-62-6 | 10MG
Cayman Chemical 3amino Benzamide
A PARP inhibitor (IC50 = 5.4 µM in C3H/10T1/2 mouse stem cells); inhibits spontaneous, as well as FGF2-induced, cell invasiveness of HUVECs at 50 µM; induces tubulogenesis and reduces FGF2-induced expression of UPA in HUVECs at 50 µM; reduces telomere length in HeLaS3 human cervical cancer cells and non-cancerous COM3 hamster cells
Cayman Chemical 3amino Benzamide
A PARP inhibitor (IC50 = 5.4 µM in C3H/10T1/2 mouse stem cells); inhibits spontaneous, as well as FGF2-induced, cell invasiveness of HUVECs at 50 µM; induces tubulogenesis and reduces FGF2-induced expression of UPA in HUVECs at 50 µM; reduces telomere length in HeLaS3 human cervical cancer cells and non-cancerous COM3 hamster cells
Cayman Chemical 4-HydroxyhIppurIc AcId 100mg
An OAT1 inhibitor (IC50 = 25 µM in opossum kidney cells); increases the production of free radicals in opossum kidney cells expressing human OAT1; reduces the secretion of TNF-α by 30.4% at 1 µM
Cayman Chemical 4-HydroxyhIppurIc AcId 250mg
An OAT1 inhibitor (IC50 = 25 µM in opossum kidney cells); increases the production of free radicals in opossum kidney cells expressing human OAT1; reduces the secretion of TNF-α by 30.4% at 1 µM
Cayman Chemical 4-HydroxyhIppurIc AcId 500mg
An OAT1 inhibitor (IC50 = 25 µM in opossum kidney cells); increases the production of free radicals in opossum kidney cells expressing human OAT1; reduces the secretion of TNF-α by 30.4% at 1 µM
Cayman Chemical 4-HydroxyhIppurIc AcId 1g
An OAT1 inhibitor (IC50 = 25 µM in opossum kidney cells); increases the production of free radicals in opossum kidney cells expressing human OAT1; reduces the secretion of TNF-α by 30.4% at 1 µM
Medchemexpress LLC 3-methoxybenzamide | 5813-86-5 | 99.4% | 10 MG
3-methoxybenzamide is a small-molecule inhibitor of ADP-ribosyltransferases (ADPRTs) and poly(ADP-ribose) polymerase (PARP) used as a research reagent and analytical standard. It affects bacterial septation via the FtsZ system and can enhance in vitro plant growth and microtuber formation.
- Used as an inhibitor in cell cycle and DNA damage studies.
- Affects bacterial cell division and septation.
- Enhances plant tissue culture microtuber formation.
- High purity (99.4%) suitable for analytical applications.
- Molecular formula C8H9NO2; molecular weight 151.16.
TARGETMOL CHEMICALS INC CORYLIFOL A 10MG
Also available in 1 mg 5 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. 1. Corylifol A (Corylinin) displays cytotoxic activity against HepG2 and Hep3B hepatocellular carcinoma cell lines with IC50 values of 4.6 and 13.5 ug/ml respectively. 2. Corylifol A and Biochanin A can be the potential uncouplers of neuronal nitric oxide synthase-postsynaptic density protein-95. 3. Corylifol A and bavachin are strong inhibitors of UDP-glucuronosyltransferase 1A1 (UGT1A1) with the inhibition kinetic parameters (Ki) values lower than 1 uM.4. Corylifol A and bakuchiol are naturally occurring potent inhibitors of hCE2 with low Ki values ranging from 0.62uM to 3.89 uM. 5. Corylifol A shows an inhibitory effect on IL-6-induced STAT3 promoter activity in Hep3B cells with IC50 values of 0.81 ± 0.15 uu it also inhibits STAT3 phosphorylation induced by IL-6 in Hep3B cells suggests that corylifol A has antiinflammatory activity. purity: 99%
TARGETMOL CHEMICALS INC NECROSTATIN-1 50MG
Also available in 5 mg 10 mg 25 mg 100 mg 200 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Necrostatin-1 (Necrostatin 1) is a specific RIP1 inhibitor and inhibits TNF-(alpha)-induced necroptosis (EC50 490 nM in Jurkat cells). purity: 99%
Medchemexpress LLC GPI-1485 (GM1485) | 186268-78-0 | 99.6% | 241.28 | 1 ML
GPI-1485 (GM1485) is a nonimmunosuppressive immunophilin ligand that promotes neurofunctional improvement and neural regeneration after a stroke. It is intended for research use only.
- Promotes neurofunctional improvement and neural regeneration
- Acts as a nonimmunosuppressive immunophilin ligand
- Induces cellular reprogramming and neural cell induction in vitro
- Improves long-term neurological recovery in vivo
- Supplied as a white to light yellow solid
Medchemexpress LLC 3-methoxybenzamide | 5813-86-5 | 99.4% | 500 MG
3-methoxybenzamide (3-MBA) is a small-molecule research compound that functions as an inhibitor of ADP-ribosyltransferases (ADPRTs) and PARP. It is provided as a solid for laboratory research and is commonly used in biochemical and cell-based studies.
- High purity of 99.4%.
- Molecular formula C8H9NO2 and molecular weight 151.16.
- Available in milligram-scale packages for laboratory research.
- Intended for research use only; not for human or animal therapeutic use.
Medchemexpress LLC GPI-1485 (GM1485) | 186268-78-0 | 99.6% | 241.28 | 25 MG
GPI-1485 (GM1485) is a nonimmunosuppressive immunophilin ligand that promotes neurofunctional improvement and neural regeneration following stroke.
- Acts as a nonimmunosuppressive immunophilin ligand.
- Promotes neurofunctional improvement.
- Supports neural regeneration following stroke.
- Induces cellular reprogramming and neural cell induction in normal human dermal fibroblasts (NHDF) in vitro.
- Improves long-term neurological recovery in rats in vivo.
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