Unsubstituted Phenols
Medchemexpress LLC Isorhamnetin-3-O-neohespeidoside | 55033-90-4 | 624.54 | 5 MG
Isorhamnetin-3-O-neohespeidoside | 55033-90-4 | 624.54 | 5 MG
Medchemexpress LLC HY-100380 5mg Medchemexpress, TPO agonist 1 CAS:1033040-23-1 Purity:>98%
Medchemexpress, HY-100380 5mg TPO agonist 1 CAS:1033040-23-1 TPO agonist 1 is a thrombopoietin (TPO) agonist extracted from patent WO2008134338A1, compound TPO mimetic. It would be useful as promoters of thrombopoiesis and megakaryocytopoiesis to treat thrombocytopenia [1] . Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC Levoleucovorin Calcium | 80433-71-2 | 99.9% | 511.50 | 500 MG
Levoleucovorin Calcium, also known as Calcium levofolinate, is the active form of calcium Folinic acid. It exhibits anti-tumor effects and acts as a potentiator for the anti-cancer toxicity of 5-Fluorouracil. This product is intended for research use only.
- Active form of calcium folinic acid
- Exhibits anti-tumor effects
- Potentiates anti-cancer toxicity of 5-Fluorouracil
- Ships at room temperature (continental US)
- Store at 4°C, sealed, away from moisture and light
- Store in solvent at -80°C for 6 months or -20°C for 1 month, sealed, away from moisture and light
- Soluble in water (7.69 mg/mL, requires sonication)
- Insoluble or slightly soluble in DMSO
- Appears as a white to yellow solid
STA PHARMACEUTICAL US LLC Fmoc-(S)-3-Amino-4-(2,4-dichloro-phenyl)-butyric acid | 50 g | CAS 270063-49-5 | MDL MFCD01861045
Fmoc-(S)-3-Amino-4-(2,4-dichloro-phenyl)-butyric acid is a Amino Acid reagent (Subcategory: Beta AA) sold by WuXi TIDES. Offered in 50 g. Store at 4 °C. SDS available for reference.
Specifications
- CAS: 270063-49-5
- MDL: MFCD01861045
- InChIKey: UAGBOWBNDBDJMF-KRWDZBQOSA-N
- Molecular Weight: 470.346
- Molecular Formula: C25H21Cl2NO4
- Purity: ≥95%
- Container Type: 250 mL HDPE
- Pack Size: 50 g
- Net Weight: 50 g
- Gross Weight: 89.8 g
- Commodity Code: 29242970
- Country Of Origin: China
- IUPAC: (S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(2,4-dichlorophenyl)butanoic acid
- SMILES: ClC1=CC(Cl)=C(C[C@H](NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O)CC(O)=O)C=C1
C1=CC(=O)c2c(O)ccc(O)c2C1=O | 100mg | 562460577](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502161116.JPG-250.jpg)
eMolecules 517-89-5 | Shikonin | Apollo Scientific | MFCD00075680 | 288.299 | C16H16O5 | 0.000 | CC(C)=CC[C@@H](O)C1=CC(=O)c2c(O)ccc(O)c2C1=O | 100mg | 562460577
Shikonin | Apollo Scientific | 517-89-5 | MFCD00075680 | 288.299 | C16H16O5 | 0.000 | CC(C)=CC[C@@H](O)C1=CC(=O)c2c(O)ccc(O)c2C1=O | 100mg | 562460577
Medchemexpress LLC (E/Z)-GSK5182 | 2699724-40-6 | 98.9% | 417.54 | 500 MG
(E/Z)-GSK5182 is a racemic compound of (E)-GSK5182 and (Z)-GSK5182 isomers. GSK5182 is a highly selective and orally active inverse agonist of estrogen-related receptor γ (ERRγ) with an IC50 of 79 nM. It also induces reactive oxygen species (ROS) generation in hepatocellular carcinoma.
- Racemic compound of (E)-GSK5182 and (Z)-GSK5182 isomers
- Highly selective and orally active inverse agonist of estrogen-related receptor γ (ERRγ)
- IC50 of 79 nM for ERRγ
- Induces reactive oxygen species (ROS) generation in hepatocellular carcinoma
- For research use only
Medchemexpress LLC Icilin | 36945-98-9 | 99.3% | 311.29 | 100 MG
Icilin (AG-3-5) is a super-agonist of the transient receptor potential M8 (TRPM8) ion channel. It activates TRPM8 in EGTA in a dose-dependent manner (EC50=1.4 μM) and is considered a "super-cooling agent". Icilin also helps to reduce autoimmune neuroinflammation by modulating the T-cell response.
- Activates TRPM8 in EGTA in a dose-dependent manner (EC50=1.4 μM).
- Considered a "super-cooling agent".
- Modulates T-cell response to reduce autoimmune neuroinflammation.
Medchemexpress LLC VL285 phenol | 1448188-69-9 | MFCD31746640 | 98.6% | 548.65 g/mol | C29H32N4O5S | 10 MG
VL285 Phenol is a phenol-based analog of a VHL E3 ligase ligand, provided as a high-purity research chemical for use as a PROTAC building block and for VHL recruitment studies. It has reported activity in degrading HaloTag7 fusion proteins (IC50 = 0.34 μM).
- Phenol-based VHL ligand analog.
- Suitable for PROTAC synthesis and VHL studies.
- High purity (98.56%).
- Molecular weight 548.65 g/mol; formula C29H32N4O5S.
- Soluble in DMSO at 100 mg/mL.
- Powder storage: -20°C (up to 3 years), 4°C (up to 2 years).
Medchemexpress LLC HY-111484 5mg Medchemexpress, GDC-0927 CAS:1642297-01-5 Purity:>98%
Medchemexpress, HY-111484 5mg GDC-0927 CAS:1642297-01-5 GDC-0927 (SRN-927) is a novel, potent, non-steroidal, orally bioavailable, selective estrogen receptor antagonist. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC Nα,Nα-bis(carboxymethyl)-L-lysine | 113231-05-3 | MFCD00237437 | 98.8% | 262.26 | C10H18N2O6 | 10 G
Nα,Nα-Bis(carboxymethyl)-L-lysine is a research-grade small molecule that competitively inhibits the bitter taste receptor T2R4, with a reported IC50 of approximately 59 nM. It is used in receptor pharmacology and cell-based assays to probe T2R4-mediated signaling; in vitro studies show reduction of basal receptor activity, while limited in vivo effects on bitter taste behavior have been reported.
- Competitive inhibitor of bitter taste receptor 4 (IC50 ≈59 nM).
- Suitable for receptor pharmacology and cell-based assays.
- Shown in vitro to reduce basal activity of constitutively active T2R4 mutants.
- Reported minimal in vivo effect on bitter taste licking behavior at 10 μM.
- High purity material (98.8%) for research use.
- Molecular weight 262.26; formula C10H18N2O6.