Unclassified Organic Compounds
eMolecules Ambeed / 5-(Pyridin-2-yl)-134-oxadiazol-2-amine / 100mg / 600841349 / A480222 / / 5711-72-8 / MFCD01710636 / 162.152 / C7H6N4O
Ambeed / 5-(Pyridin-2-yl)-134-oxadiazol-2-amine / 100mg / 600841349 / A480222 / / 5711-72-8 / MFCD01710636 / 162.152 / C7H6N4O
Isooctadecenylsuccinic Anhydride (mixture of branched chain isomers) 90.0+%, TCI America™
CAS: 58239-72-8 Molecular Formula: C22H38O3 Molecular Weight (g/mol): 350.54 MDL Number: MFCD00070628 InChI Key: SJSHEXCFGWSYAD-VURMDHGXNA-N
N-Benzylnortropinone 95.0+%, TCI America™
CAS: 28957-72-4 Molecular Formula: C14H17NO Molecular Weight (g/mol): 215.30 MDL Number: MFCD00151640 InChI Key: RSUHKGOVXMXCND-UHFFFAOYNA-N Synonym: 8-benzyl-8-azabicyclo 3.2.1 octan-3-one,n-benzylnortropinone,n-benzyltropinone,8-benzyl-8-aza-bicyclo 3.2.1 octan-3-one,8-phenylmethyl-8-azabicyclo 3.2.1 octan-3-one,8-azabicyclo 3.2.1 octan-3-one, 8-phenylmethyl,n-benzyl tropinone,8-benzyl-8-azabicyclo 3.2.1 octan-3-on,n-benzyl-8-azabicyclo 3.2.1 octan-3-one PubChem CID: 119846 IUPAC Name: 8-benzyl-8-azabicyclo[3.2.1]octan-3-one SMILES: O=C1CC2CCC(C1)N2CC1=CC=CC=C1
Medchemexpress LLC Lonicerin (Veronicastroside) | 25694-72-8 | 5 MG
Lonicerin (Veronicastroside) is a flavonoid that exhibits a range of biological activities. It functions as an inhibitor of xanthine oxidase and alginate secretion protein (AlgE). Additionally, Lonicerin demonstrates anti-inflammatory, anti-arthritic, antioxidant, antifungal, anti-bacterial, and neuroprotective properties.
- Inhibits xanthine oxidase, alginate secretion protein (AlgE), P. aeruginosa, and C. albicans.
- Possesses anti-inflammatory, anti-arthritic, and neuroprotective properties.
- Acts as an antioxidant, scavenging DPPH, hydroxyl, and superoxide radicals.
- Reduces alginate secretion and biofilm formation.
- Suppresses T cell proliferation and inhibits nitric oxide production from macrophages.
- Reduces paw edema in a mouse model of C. albicans arthritis.
Medchemexpress LLC α-Zearalenol | 36455-72-8 | 10 MG
Alpha-Zearalenol is a mycotoxin exhibiting high affinity for estrogen receptors (ER). This derivative of zearalenone (ZEN) is known for causing reproductive disorders in animals due to its xenoestrogenic effects. It is a solid, white to off-white compound with a molecular weight of 320.38 and a chemical formula of C18H24O5. This product is intended for research use only and not for patient administration.
- Exhibits high affinity for estrogen receptors (ER)
- Causes reproductive disorders due to xenoestrogenic effects
- Inhibits cytotoxicity against human KB cells (IC50 100.29 μM)
- Inhibits cytotoxicity against African green monkey Vero cells (IC50 60.33 μM)
- Increases cell viability in MCF-7 cells
- Reduces TNF-α expression
- Induces cell cycle changes in MCF7 cells (S phase and G2/M phase)
Medchemexpress LLC Α-Zearalenol | 36455-72-8 | 5 MG
Alpha-Zearalenol is a mycotoxin that exhibits high affinity for estrogen receptors (ER). This derivative of zearalenone (ZEN) is known to induce reproductive disorders in animals through its xenoestrogenic effects and is intended for research use only.
- Cytotoxicity in KB cells with an IC50 of 100.29 μM.
- Cytotoxicity in Vero cells with an IC50 of 60.33 μM.
- In MCF-7 cells, it shows an IC50 of 12.5 μM and increases cell viability and population in S and G2/M phases.
- Slightly cytotoxic to MDA-MB231 cells, with no visible change in cell cycle phases.
- Reduces TNF-α expression in HepG2 cells; combined with β-ZOL, it acts antagonistically for IL-1β and synergistically for IL-8 at higher concentrations.
Sigma Aldrich Fine Chemicals Biosciences alpha-Zearalenol | 36455-72-8 | MFCD16657008 | 10MG
alpha-Zearalenol | Purity: >=98% (HPLC) | Mol Wt: 320.38 | 36455-72-8 | MFCD16657008 | 10MG
Sigma Aldrich Fine Chemicals Biosciences alpha-Zearalenol | 36455-72-8 | MFCD16657008 | 5MG
alpha-Zearalenol | Purity: >=98% (HPLC) | Mol Wt: 320.38 | 36455-72-8 | MFCD16657008 | 5MG
Chem-Impex International, Inc. Colistin sulfate, nonsterile | 1264-72-8 | MFCD27976775 | 1G
Colistin sulfate, nonsterile, 1264-72-8, MFCD27976775, 1G
Sigma Aldrich Fine Chemicals Biosciences Colistin sulfate salt | 1264-72-8 | MFCD00146495 | 100mg
Colistin sulfate salt | 1264-72-8 | MFCD00146495 | 100mg
eMolecules 5-Phenoxypentyl bromide | 22921-72-8 | MFCD00039203 | 1g
Combi-Blocks | 5-Phenoxypentyl bromide | 1g | 457920178 | QH-3038 | 95.000 | 22921-72-8 | MFCD00039203 | 243.144 | C11H15BrO
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Medchemexpress LLC HS-276 | 2767422-72-8 | 98.9% | 419.52 | 5 MG
HS-276 is an orally active, potent, and highly selective TAK1 inhibitor with a Ki of 2.5 nM. It significantly inhibits multiple kinases including TAK1, CLK2, GCK, ULK2, MAP4K5, IRAK1, NUAK, CSNK1G2, CAMKKβ-1, and MLK1. It reduces the expression of TNF, IL-6, and IL-1β in a dose-dependent manner and shows excellent bioavailability in mice, making it suitable for rheumatoid arthritis (RA) research.
- Orally active and highly selective TAK1 inhibitor
- Significant inhibition of multiple kinases
- Reduces expression of inflammatory cytokines
- Demonstrates excellent bioavailability in vivo
- Suitable for rheumatoid arthritis research
Sigma Aldrich Fine Chemicals Biosciences Colistin Sulfate Salt | 1264-72-8 | MFCD00146495 | 1g
Colistin Sulfate Salt | Mol Wt: 1267.55 | 1264-72-8 | MFCD00146495 | 1g
Sigma Aldrich Fine Chemicals Biosciences Ammonium citrate tribasic | 3458-72-8 | MFCD00036406 | 500g
Ammonium citrate tribasic | Purity: 97% | MW: 243.22 | 3458-72-8 | MFCD00036406 | 500g
Medchemexpress LLC Cndac hydrochloride | 134665-72-8 | 98.01% | 288.69 | 100 MG
CNDAC hydrochloride is a metabolite of the orally active agent Sapacitabine (HY-16445), and a nucleoside analog. It induces DNA damage and apoptosis.
- Metabolite of Sapacitabine (HY-16445)
- Nucleoside analog
- Induces DNA damage
- Induces apoptosis