Vinyl halides
eMolecules 10485-09-3 | 2-Bromoindene | Ambeed | MFCD06797863 | 195.059 | C9H7Br | 98.000 | BrC1=Cc2ccccc2C1 | 1g | 552527369
2-Bromoindene | Ambeed | 10485-09-3 | MFCD06797863 | 195.059 | C9H7Br | 98.000 | BrC1=Cc2ccccc2C1 | 1g | 552527369
Sigma Aldrich Fine Chemicals Biosciences 3 3-DIMETHYL-1-BUTENE 97 GC
NC3739483 3 3-DIMETHYL-1-BUTENE 97 GC
Medchemexpress LLC Rp-8-Br-cAMPS sodium | 925456-59-3 | 446.15 | 500 UG
Rp-8-Br-cAMPS sodium is an analog of cAMP and an inhibitor of PKA. It occupies cAMP binding sites on PKA type I regulatory subunits, which prevents PKA dissociation and activation. It can be used in the study of tumors and retrovirus-induced immune deficiency, and it also inhibits insulin secretion.
- Blocks the ability of 2-chloroadenosine to inhibit LAK cytotoxicity.
- Significantly reduces the inhibitory effect of 2-chloroadenosine on cytokine production.
- Inhibits insulin secretion in 832/13 cells.
- Improves immune function in a mouse retrovirus infection model.
- Strongly increases responses to the anti-CD3 mAb.
- Improved T cell responses.
Medchemexpress LLC Prexigebersen sodium | 202484-91-1 | 95.6% | 5520.6 (free acid) | C177H206N63Na18O110P17 | 10 MG
Prexigebersen sodium is a liposomal-formulated antisense oligonucleotide designed to inhibit synthesis of the adaptor protein Grb2. Supplied as a characterized sodium salt for research use, it is intended for preclinical studies of Grb2-mediated signaling pathways and oncology-related investigations.
- Antisense oligonucleotide targeting Grb2.
- Liposomal formulation for enhanced delivery.
- Sodium salt form for aqueous solubility.
- High purity suitable for research applications.
- Available in small-scale research quantities.
- Includes documentation: datasheet, SDS, COA, and LCMS.
Medchemexpress LLC Silmitasertib sodium salt (CX-4945 sodium salt) | 1309357-15-0 | 99.9% | C19H11ClN3NaO2 | 50 MG
Silmitasertib sodium salt is an orally bioavailable, highly selective, and potent CK2 inhibitor, demonstrating IC50 values of 1 nM against CK2α and CK2α'. This compound induces cell-cycle arrest and selectively promotes apoptosis in cancer cells. It also attenuates PI3K/Akt signaling, decreases pro-survival ER chaperon BIP/Grp78 expression, and suppresses activation of CK2-mediated PI3K/Akt/mTOR signaling pathways in hematological tumors.
- Orally bioavailable and potent CK2 inhibitor
- Highly selective against CK2α and CK2α' (IC50 1 nM)
- Induces cell-cycle arrest and apoptosis in cancer cells
- Attenuates PI3K/Akt signaling
- Suppresses CK2-mediated PI3K/Akt/mTOR signaling
Medchemexpress LLC Dicloxacillin sodium | 343-55-5 | 98.0% | 25 MG
Dicloxacillin sodium is a β-lactam antibiotic belonging to the penicillin family. It is effective against Gram-positive bacteria and β-lactamase-producing organisms, such as Staphylococcus aureus.
- Effective against Gram-positive bacteria
- Active against β-lactamase-producing organisms
- Purity of 98.0%
- CAS No. 343-55-5
- Molecular Weight: 492.31
- Formula: C19H16Cl2N3NaO5S
- Appearance: Solid
- Color: White to off-white