Glycosyl compounds
eMolecules 2168552-79-0 | 1-METHYLCYCLOBUTANE-1,3-DIOL | AstaTech102.133 | C5H10O2 | 95.000 | CC1(O)CC(O)C1 | 0.1g | 801703731
1-METHYLCYCLOBUTANE-1,3-DIOL | AstaTech | 2168552-79-0102.133 | C5H10O2 | 95.000 | CC1(O)CC(O)C1 | 0.1g | 801703731
Medchemexpress LLC Cytochalasin D | 22144-77-0 | 1 ML
Cytochalasin D, also known as Zygosporin A, is a potent, cell-permeable actin polymerization inhibitor derived from fungus. It functions by inhibiting the G-actin-cofilin interaction and the binding of cofilin to F-actin, which consequently decreases the rates of both actin polymerization and depolymerization in living cells.
- Potent actin polymerization inhibitor
- Cell-permeable activity
- Inhibits G-actin-cofilin interaction
- Decreases actin polymerization and depolymerization rates
- Reduces exosome release and survivin in tumor environment
- Induces phosphorylation and cytoplasmic retention of Yap
- Causes retraction and arborization of COS-7 cells
- Disrupts stress fibers in NIH3T3 cells
Chem-Impex International, Inc. a-D-Lactose monohydrate | 5989-81-1 | MFCD00150747 | 5KG
a-D-Lactose monohydrate, 5989-81-1, MFCD00150747, 5KG
Medchemexpress LLC Inosine pranobex | 36703-88-5 | 98.1% | 1115.23 g/mol | C52H78N10O17 | 100 MG
Inosine pranobex is an orally active immunomodulator supplied for research and analytical use. It exhibits broad-spectrum antiviral activity and is commonly used in virology and immunology studies to evaluate antiviral and immune-modulating effects in vitro.
- Orally active immunomodulator.
- Broad-spectrum antiviral activity against multiple DNA and RNA viruses.
- Research-grade purity: 98.1%.
- Molecular weight 1115.23 g/mol.
- Available as solids (for example, 100 mg and larger) and as 10 mM solutions in DMSO.
- Intended for in vitro and analytical research applications.
Chem-Impex International, Inc. D(+)-Trehalose dihydrate | 6138-23-4 | MFCD00071594 | 100G
D(+)-Trehalose dihydrate, 6138-23-4, MFCD00071594, 100G
Chem-Impex International, Inc. D(+)-Cellobiose | 528-50-7 | MFCD00065388 | 100G
D(+)-Cellobiose, 528-50-7, MFCD00065388, 100G
Apexbio Technology LLC Cytochalasin D 22144-77-0 1mg
Cytochalasin D is a selective inhibitor of actin polymerization with a reported IC50 value of approximately 25 nM It exerts its biological effect by disrupting the formation and stability of actin filaments thereby influencing cellular processes dependent on cytoskeletal organization Through this mechanistic action Cytochalasin D induces cell cycle arrest at the G1-S transition via activation of p53-related signaling pathways In neuronal studies treatment with Cytochalasin D interferes with filopodial and lamellipodial dynamics by limiting protrusion elongation Additionally in vitro investigations demonstrated its utility in the study of virus-host interactions where blockade of actin polymerization inhibits pathogen entry and replication making Cytochalasin D a relevant reagent in cellular biology and virology research
Medchemexpress LLC [Ala11,D-Leu15]-Orexin B(human) | 532932-99-3 | 98.3% | 2857.26 | 1 MG
[Ala11,D-Leu15]-Orexin B(human) is a potent and selective orexin-2 receptor (OX2) agonist, demonstrating a 400-fold selectivity for OX2 (EC50=0.13 nM) over OX1 (52 nM). This peptide is supplied as a solid, white to off-white in color, with a purity of 98.31%.
- Potent and selective orexin-2 receptor (OX2) agonist
- Shows 400-fold selectivity for OX2 (EC50=0.13 nM) over OX1 (52 nM)
- CAS number: 532932-99-3
- Molecular weight: 2857.26
- Formula: C120H206N44O35S
- Sequence: Arg-Ser-Gly-Pro-Pro-Gly-Leu-Gln-Gly-Arg-Ala-Qln-Arg-Leu-{dLeu}-Gln-Ala-Ser-Gly-Asn-His-Ala-Ala-Gly-Ile-Leu-Thr-Met-NH2
- Store sealed, away from moisture and light, under nitrogen
- Powder stability: -80°C for 2 years, -20°C for 1 year
- In solvent stability: -80°C for 6 months, -20°C for 1 month
Medchemexpress LLC Plantainoside D | 147331-98-4 | 5 MG
Plantainoside D is a phenylethanoid glycoside and an IKK-β inhibitor with diverse biological activities. It shows inhibitory activity of angiotensin-converting enzyme (ACE) and reduces glutamate release from nerve terminals. It also alleviates cell apoptosis and improves acute lung injury (ALI) induced by sepsis, making it suitable for studies in neuroprotection, antioxidant, anti-inflammation, and antihypertension.
- Phenylethanoid glycoside and an IKK-β inhibitor
- Inhibits angiotensin-converting enzyme (ACE) with an IC50 of 2.17 mM
- Reduces glutamate release from nerve terminals by inhibiting voltage-dependent calcium channels and protein kinase C signaling
- Alleviates cell apoptosis by inhibiting ROS generation and NF-κB activation
- Improves acute lung injury (ALI) induced by sepsis by regulating the Sirt3/NLRP3 signaling pathway
![eMolecules 209347-94-4 | 5-Bromo-6-chloro-3-indolyl caprylate | Apollo Scientific | MFCD00798386 | 372.690 | C16H19BrClNO2 | 0.000 | CCCCCCCC(=O)Oc1c[nH]c2cc(Cl)c(Br)cc12 | 1g | 562432813](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502160296.JPG-250.jpg)
eMolecules 209347-94-4 | 5-Bromo-6-chloro-3-indolyl caprylate | Apollo Scientific | MFCD00798386 | 372.690 | C16H19BrClNO2 | 0.000 | CCCCCCCC(=O)Oc1c[nH]c2cc(Cl)c(Br)cc12 | 1g | 562432813
5-Bromo-6-chloro-3-indolyl caprylate | Apollo Scientific | 209347-94-4 | MFCD00798386 | 372.690 | C16H19BrClNO2 | 0.000 | CCCCCCCC(=O)Oc1c[nH]c2cc(Cl)c(Br)cc12 | 1g | 562432813
Sigma Aldrich Fine Chemicals Biosciences 5-Bromo-4-chloro-3-indolyl beta-D-galactopyranoside >=98%, powder | 7240-90-6 | MFCD00005666 | 100MG
5-Bromo-4-chloro-3-indolyl beta-D-galactopyranoside >=98%, powder | Purity: >=98% | Mol Wt: 408.63 | 7240-90-6 | MFCD00005666 | 100MG
AdipoGen Ectoine ultrapure
Natural chemical product. CAS 96702-03-3. Formula C6H10N2O2. MW 142.2. Isolated from halophilic bacteria Halomonas elongata. The ectoines belong to the class of compatible solutes also called extremolytes osmolytes from extremophiles. Extremolytes stabilize biological structures and macromolecules such as lipid membranes and proteins against a variety of stress factors, including high temperature, freeze-thaw cycles, drying and degradation. These very stable, non-toxic, animal-free protective agents are powerful additives in various Life Science applications, ranging from cryoprotection of animal cells over protein storage to PCR. They are protective osmolytes selected by nature for stabilization of all proteins in the cell against denaturing environmental stress without altering their functional activity. The stabilizing effect is based on the fact, that the protective osmolytes are strong water-structure formers and as such are preferentially excluded from the protein surface.
Pfanstiehl Inc Sucrose USP-NF, EP, JP, ChP High Purity, Low Endotoxin, Low Metals (Beet Derived) (S-124-2-MC) 100G GMP, Multi-Compendial CAS: 57-50-1 Injectable Excipient Grade
Pfanstiehl Sucrose (Beet Derived) - High Purity, Low Endotoxin, Low Metals is a multi-compendial stabilizer of proteins, lipids, and carbohydrates in biologic therapeutics. Used throughout formulation and freeze/thaw cycles, it ensures stability and efficacy in biopharmaceutical applications. Manufactured in the USA under ICH-Q7 cGMP conditions, Pfanstiehl Sucrose meets parenteral (injectable) excipient grade standards, making it ideal for biologic and vaccine formulations. It is also widely used in cryopreservation media to protect cell membranes and enhance cell recovery for bioproduction and cell therapy. Pfanstiehl Brand Sucrose is multi-compendial and available as USP-NF (National Formulary), EP (Ph. Eur.) (European Pharmacopoeia), JP (Japanese Pharmacopoeia), and ChP (Chinese Pharmacopoeia) Compendial Sucrose, GMP Sucrose, cGMP sucrose, sucrose excipient, injectable sucrose, pharmaceutical sucrose, U.S.P. sucrose, multicompendial
TARGETMOL CHEMICALS INC NF-56-EJ40 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. NF-56-EJ40 is an effective and highly selective antagonist of human SUCNR1 with an IC50 of 25 nM and a Ki of 33 nM. purity: 98%