Unclassified Organic Compounds
4-Hydroxy-L-(+)-2-phenylglycine 99.0+%, TCI America™
CAS: 32462-30-9 Molecular Formula: C8H9NO3 Molecular Weight (g/mol): 167.164 MDL Number: MFCD00065932 InChI Key: LJCWONGJFPCTTL-ZETCQYMHSA-N Synonym: (S)-(+)-2-Amino-2-(4-hydroxyphenyl)acetic Acid, L-(+)-2-(4-Hydroxyphenyl)glycine, Oxfenicine, H-Phg(4-OH)-OH PubChem CID: 36143 ChEBI: CHEBI:31755 IUPAC Name: (2S)-2-amino-2-(4-hydroxyphenyl)acetic acid SMILES: C1=CC(=CC=C1C(C(=O)O)N)O
Sigma Aldrich Fine Chemicals Biosciences GW4064|278779-30-9 | MFCD09971006 | 25mg
GW4064 | Purity: 97% (HPLC) | MW: 542.84 | 278779-30-9 | MFCD09971006 | 25mg
Enzo Life Sciences Fusicoccin (1mg). CAS: 20108-30-9
Diterpene glucoside with numerous effects. Induces H+ extrusion from plant cells by 14-3-3-dependent activation of the plasma membrane H+-ATPase. It induces translocation of 14-3-3 proteins from the cytosol to the membrane and causes a dramatic increase in cytosolic 14-3-3s. Stimulates release of cytochrome c from mitochondria, cell enlargement, ion uptake, seed germination, opening the stomata, etc. Markedly reduces the cell’s capability for H2O2 scavenging. Fusicoccin has been demonstrated to cause randomization of asymmetry of the left-right axis (heterotaxia) in Xenopus embryos. Purity: ≥90% (HPLC). Solubility: Soluble in ethanol and chloroform. Slightly soluble in ethyl acetate, ethyl ether, sparingly soluble in acetone. Long Term Storage: -20°C.
Sigma Aldrich Fine Chemicals Biosciences GW4064 | 278779-30-9 | MFCD09971006 | 5 mg
GW4064 | Purity: ≥97% | Mol Wt: 542.84 | 278779-30-9 | MFCD09971006 | 5 mg
Sigma Aldrich Fine Chemicals Biosciences PBIT >=98% (HPLC) | 2514-30-9 | 25MG
PBIT >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 241.31 | 2514-30-9 | 25MG
Sigma Aldrich Fine Chemicals Biosciences PBIT >=98% (HPLC) | 2514-30-9 | 5MG
PBIT >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 241.31 | 2514-30-9 | 5MG
Medchemexpress LLC ASP4132 | 1640294-30-9 | 99.8% | 937.06 | 50 MG
ASP4132 is an orally active, potent AMPK activator with an EC50 of 18 nM. It demonstrates significant anti-cancer activity and induces tumor regression in breast cancer xenograft mouse models.
- Potent AMPK activator with an EC50 of 18 nM.
- Exhibits anti-cancer activity.
- Induces tumor regression in breast cancer xenograft models.
- Shows cell growth inhibitory activity against MDA-MB-453 breast cancer cells.
- Stable in human liver microsomes.
Medchemexpress LLC Asp4132 | 1640294-30-9 | 99.8% | 937.06 | 100 MG
ASP4132 is an orally active, potent AMPK activator with an EC50 of 18 nM. It demonstrates anti-cancer activity and induces tumor regression in breast cancer xenograft mouse models. It is for research use only.
- Potent AMPK activator
- Exhibits anti-cancer activity
- Induces tumor regression in breast cancer models
- Orally active compound
- Suitable for in vitro and in vivo studies
Medchemexpress LLC Balovaptan | 1228088-30-9 | 99.9% | 409.91 | 10 MG
Balovaptan (RG7314) is an orally available, selective brain-penetrant vasopressin 1a (hV1a) receptor antagonist. It is characterized by its high selectivity for hV1a receptors and is commonly used in research related to autism.
- Orally available
- Selective brain-penetrant vasopressin 1a (hV1a) receptor antagonist
- High selectivity for hV1a receptors over hV2 and hOTR
- Utilized in autism research
Medchemexpress LLC MLT-748 100mg | 1832578-30-9 | 100 MG
MLT-748 is a potent, selective, allosteric inhibitor of MALT1 that binds the Trp580 pocket and inhibits protease activity with an IC50 of ~5 nM. It is supplied for biochemical and cellular studies to probe MALT1-dependent signaling and preclinical research.
- Potent MALT1 inhibition (IC50 ~5 nM).
- Allosteric mechanism by binding the Trp580 pocket.
- High purity suitable for research applications.
- Available as solid or DMSO solution for assay convenience.
- Stable under recommended storage conditions for long-term use.
Medchemexpress LLC Balovaptan | 1228088-30-9 | 99.9% | 409.91 | 50 MG
Balovaptan is an orally available, selective brain-penetrant vasopressin 1a (hV1a) receptor antagonist. It is utilized in autism research and exhibits high selectivity for its target receptors.
- Orally available
- Selective brain-penetrant vasopressin 1a (hV1a) receptor antagonist
- Ki values of 1 nM for human (hV1a) and 39 nM for mouse (mV1a) receptors
- Greater than 30000-fold selectivity for hV1a over hV2 receptors
- 9891-fold selectivity over human oxytocin receptor (hOTR)
Sigma Aldrich Fine Chemicals Biosciences Dodecyl methyl sulfoxide | 3079-30-9 | MFCD02326311 | 1g
Dodecyl methyl sulfoxide | Purity: 98% | Mol Wt: 232.43 | 3079-30-9 | MFCD02326311 | 1g
Sigma Aldrich Fine Chemicals Biosciences VU0405601 >=98% (HPLC) | 712325-30-9 | MFCD05995040 | 25MG
VU0405601 >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 357.2 | 712325-30-9 | MFCD05995040 | 25MG
Medchemexpress LLC Asp4132 tosylate | 1640294-30-9 | 99.8% | C46H51F3N6O8S2 | 10MG
ASP4132 is an orally active, potent AMPK activator (EC50 18 nM) that exhibits antineoplastic activity and induces tumor regression in breast cancer xenograft models. It is provided as a solid tosylate salt with high purity and is suitable for in vitro and in vivo research when prepared in appropriate solvents.
- Potent AMPK activation with low nanomolar EC50.
- Demonstrated antitumor efficacy in xenograft models.
- High chemical purity for reproducible results.
- Solid tosylate salt form for improved handling.
- High DMSO solubility for in vitro dosing.
- Multiple pack sizes available for flexible scaling.
Medchemexpress LLC Methyl pheophorbide a | 5594-30-9 | 606.71 | 1 MG
Methyl pheophorbide a is a natural product and one of the chlorophyll-a derivatives. It acts as a photosensitizer that generates singlet oxygen and reactive oxygen species (ROS) when exposed to light of a specific wavelength, which subsequently leads to cell death.
- Natural product
- Chlorophyll-a derivative
- Photosensitizer that produces singlet oxygen and reactive oxygen species (ROS) under light of specific wavelength
- Leads to cell death