Unsubstituted Phenols
Sigma Aldrich Fine Chemicals Biosciences ACES BioXtra 99.0 titratio250G
ACES BioXtra 99.0 titratio250G
Medchemexpress LLC Tyrphostin AG1296 | 146535-11-7 | 99.7% | 266.29 | 50 MG
Tyrphostin AG1296 is a potent and selective inhibitor of platelet-derived growth factor receptor (PDGFR) with an IC50 of 0.8 μM. It inhibits the signaling of human PDGF α- and β-receptors, as well as the related stem cell factor receptor (c-Kit). This compound also acts as a potent inhibitor of FLT3.
- Potent and selective inhibitor of platelet-derived growth factor receptor (PDGFR)
- Inhibits human PDGF α- and β-receptors
- Targets stem cell factor receptor (c-Kit)
- Potent inhibitor of FLT3
STA PHARMACEUTICAL US LLC Fmoc-(S)-3-Amino-4-(2,4-dichloro-phenyl)-butyric acid | 25 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 25 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: 125 mL HDPE
- Pack Size: 25 g
- Net Weight: 25 g
- Gross Weight: 54.3 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
Sigma Aldrich Fine Chemicals Biosciences Tyrphostin A9 solid | 10537-47-0 | MFCD00209853 | 5MG
Tyrphostin A9 solid | Purity: >=98% (HPLC) | Mol Wt: 282.38 | 10537-47-0 | MFCD00209853 | 5MG
eMolecules 131359-24-5 | (1E,4E)-1,5-Bis(2-hydroxyphenyl)penta-1,4-dien-3-one | MFCD01790784 | 50mg
Ambeed | N-(2-Amino-2-oxoethyl)-NN-dimethyldodecan-1-aminium chloride | 250mg | 600830288 | A1372734 | 15538-15-5 | 306.920 | C16H35ClN2O
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Medchemexpress LLC Rki-1447 dihydrochloride | 1782109-09-4 | 99.9% | 399.29 | 10 MG
RKI-1447 dihydrochloride is a potent and selective ROCK inhibitor, effectively suppressing colorectal carcinoma cell growth and promoting apoptosis. It functions by inhibiting ROCK1 (IC50 14.5 nM) and ROCK2 (IC50 6.2 nM), without affecting AKT, MEK, and S6 kinase phosphorylation. This compound has demonstrated significant anticancer activity in both in vitro and in vivo studies, including the inhibition of mammary tumor growth and antitumor effects in colorectal carcinoma.
- Potent and selective ROCK inhibitor
- Suppresses colorectal carcinoma cell growth
- Promotes apoptosis in a dose-dependent manner
- Inhibits phosphorylation of ROCK substrates MLC-2 and MYPT-1
- Exhibits anticancer activity in colorectal carcinoma (CRC)
- Inhibits mammary tumor growth in transgenic mice
- Shows antitumor activity in CRC without physiological toxicity
Sigma Aldrich Fine Chemicals Biosciences Hemin BioXtra from Porcine25G
Hemin BioXtra from Porcine25G
eMolecules 588-05-6 | 3-(2-Amino-ethyl)-phenol | J & W PharmLab LLC | MFCD06654561 | 137.182 | C8H11NO | 96.000 | NCCc1cccc(O)c1 | 5g | 289350884
3-(2-Amino-ethyl)-phenol | J & W PharmLab LLC | 588-05-6 | MFCD06654561 | 137.182 | C8H11NO | 96.000 | NCCc1cccc(O)c1 | 5g | 289350884
Medchemexpress LLC HY-76569 5mg Medchemexpress, Desfesoterodine CAS:207679-81-0 Purity:>98%
Medchemexpress, HY-76569 5mg Desfesoterodine CAS:207679-81-0 Desfesoterodine (PNU-200577) is a potent and selective muscarinic receptor (mAChR) antagonist with a KB and a pA2 of 0.84 nM and 9.14, respectively. Desfesoterodine is a major pharmacologically active metabolite of Tolterodine (PNU-200583; HY-A0024) and Fesoterodine (HY-70053). Desfesoterodine improves cerebral infarction induced detrusor overactivity in rats[4]. 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 (S,R,S)-AHPC-phenol-alkylC6-amine dihydrochloride | 2376990-28-0 | 98.2% | 660.70 | 25 MG
(S,R,S)-AHPC-phenol-alkylC6-amine dihydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the VH032 based VHL ligand and an alkyl linker used for PROTAC degrader. This product is for research use only and not sold to patients.
- Synthesized E3 ligase ligand-linker conjugate
- Incorporates VH032 based VHL ligand
- Uses an alkyl linker for degrader
- For research use only
Medchemexpress LLC HY-20019 5mg Medchemexpress, L-165041 CAS:79558-09-1 Purity:>98%
Medchemexpress, HY-20019 5mg L-165041 CAS:79558-09-1 L-165041 is a cell permeable PPARδ agonist, with Kis of 6 nM and appr 730 nM for PPARδ and PPARγ, respectively, and induces adipocyte differentiation in NIH-PPARδ cells. 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.
Sigma Aldrich Fine Chemicals Biosciences Phenol Red sodium salt pow50G
Phenol Red sodium salt pow50G