Unsubstituted Phenols
Medchemexpress LLC HY-10210 1mg Medchemexpress, Retaspimycin (Hydrochloride) CAS:857402-63-2 Purity:>98%
Medchemexpress, HY-10210 1mg Retaspimycin (HCl) CAS:857402-63-2 Retaspimycin Hydrochloride is a potent and water-soluble inhibitor of Hsp90 with EC50s of 119 nM for both Hsp90 and Grp9. 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 Syringaresinol diglucoside | 66791-77-3 | MFCD24369676 | 99.7% | 742.72 | C34H46O18 | 10 MG
Syringaresinol diglucoside is a natural lignan glycoside isolated from plant sources such as bamboo leaves. It is provided as a high-purity analytical standard for research use in biochemical, pharmacological, and analytical studies.
- Natural lignan glycoside isolated from plant sources.
- High purity (99.7%) suitable for analytical and in vitro studies.
- Molecular formula C34H46O18; molecular weight 742.72.
- CAS number 66791-77-3 for unambiguous identification.
- Supplied in milligram-scale quantities intended for research use.
Enzo Life Sciences Tyrphostin 8 (10mg). CAS: 3785-90-8
The tyrphostins are well known tyrosine kinase inhibitors. However, tyrphostin 8 has been shown to inhibit calcineurin (IC50=21 µM) while displaying weak inhibition of EGFR tyrosine kinase (IC50=560 µM). Alternative name: alpha-Cyano-(4-hydroxy)cinnamonitrile. Purity: ≥98% (TLC). Solubility: Soluble in 100% ethanol (25mg/ml) or DMSO (25mg/ml). Long Term Storage: Ambient.
eMolecules 102841-43-0 | Medchem Express | Mulberroside C | 5mg | 589794234 | HY-N0620 | MFCD20527296 | 458.463 | C24H26O9
Medchem Express | EC23 | 5mg | 506403850 | HY-12309 | 104561-41-3 | MFCD18086921 | 332.443 | C23H24O2
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eMolecules 28371-16-6 | Medchem Express | Aloin B | 5mg | 446275499 | HY-N0886 | MFCD00869345 | 418.398 | C21H22O9
Ambeed | 4-Fluoro--nitrostyrene | 5g | 572954475 | A417856 | 706-08-1 | MFCD00024824 | 167.139 | C8H6FNO2
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eMolecules 52452-60-5 | Medchem Express | Terphenyllin | 1mg | 455326185 | HY-119821 | MFCD08274598 | 338.359 | C20H18O5
Medchem Express | Terphenyllin | 1mg | 455326185 | HY-119821 | 52452-60-5 | MFCD08274598 | 338.359 | C20H18O5
Medchemexpress LLC HY-112130 10mg Medchemexpress, AGI-24512 CAS:2201066-53-5 Purity:>98%
Medchemexpress, HY-112130 10mg AGI-24512 CAS:2201066-53-5 AGI-24512 is a methionine adenosyltransferase 2A (MATA2 ) inhibitors useful for treatment of cancer. AGI-24512 blocks growth of MTAP-deleted cancer cells in vitro. 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 6H-Dibenz[b,d]oxocin-7(8H)-one, 3,10,11-trihydroxy- | 102036-28-2 | 99.98% | 272.25 | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000436001-Logo.png-250.jpg){kind=logo}
Medchemexpress LLC 6H-Dibenz[b,d]oxocin-7(8H)-one, 3,10,11-trihydroxy- | 102036-28-2 | 99.98% | 272.25 | 10 MG
6H-Dibenz[b,d]oxocin-7(8H)-one, 3,10,11-trihydroxy- | 102036-28-2 | 99.98% | 272.25 | 10 MG
eMolecules 102212-26-0 | Medchem Express | ARN2966 | 5mg | 446268991 | HY-18292 | MFCD24550644 | 200.241 | C12H12N2O
Medchem Express | Maprotiline (hydrochloride) | 100mg | 446272751 | HY-B0444 | 10347-81-6 | 313.870 | C20H24ClN
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eMolecules 487-39-8 | Medchem Express | Phillygenin | 5mg | 446275115 | HY-N0483 | MFCD01075148 | 372.417 | C21H24O6
Medchem Express | DDO-2093 (dihydrochloride) | 5mg | 742367618 | HY-132233A | | 687.040 | C29H39Cl3FN9O3
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Medchemexpress LLC SN-011 | 2249435-90-1 | 99.9% | C25H19FN2O4S | 100 MG
SN-011 is a potent and selective mouse and human STING inhibitor with an IC50 of 76 nM for STING signaling. It competes with cyclic dinucleotide (CDN) for the STING dimer binding pocket, blocking CDN binding and activation. This product is used for research into STING-driven autoimmune and inflammatory diseases.
- Suppresses STING stimulator-induced expression of Ifnb, Cxcl10, and Il6 mRNA in mouse embryonic fibroblasts.
- Inhibits 2′3′-cGAMP-induced Ifnb expression and STING oligomerization/phosphorylation.
- Suppresses STING ER-to-Golgi translocation.
- Inhibits inflammation and autoimmunity in vivo.
- Protects Trex1-/- mice from death, improves survival, and reduces multiorgan inflammation.
Medchemexpress LLC Isovitexin 2"-O-arabinoside | 53382-71-1 | 5 MG
Isovitexin 2''-O-arabinoside is a flavonoid found in plantlets of Avena sativa L. It increases alkaline phosphatase (ALP) activity and promotes BMP-2-induced osteoblast differentiation in C2C12 cells at concentrations from 0-10 μM over 3 days. It is for research use only.
- Flavonoid found in Avena sativa L. plantlets
- Increases alkaline phosphatase (ALP) activity
- Promotes BMP-2-induced osteoblast differentiation
- Targets phosphatase
- Involved in metabolic enzyme/protease pathway
Sigma Aldrich Fine Chemicals Biosciences Phenol Red sodium salt pow50G
Phenol Red sodium salt pow50G
Medchemexpress LLC (S,R,S)-AHPC-phenol-alkylC6-amine dihydrochloride | 2376990-28-0 | 98.2% | C30H47Cl2N5O5S | 10MG
(S,R,S)-AHPC-phenol-alkylC6-amine dihydrochloride is a VH032-derived VHL E3 ligase ligand-linker conjugate provided as the dihydrochloride salt. It serves as a building block for PROTAC degraders and related chemical biology reagents, offering a functionalized phenol-alkyl spacer for conjugation to target ligands.
- High purity (98.2%) suitable for synthetic and biological applications.
- Available as a solid with light yellow to yellow appearance.
- Includes a functionalized phenol-alkyl C6 amine linker for conjugation.
- Molecular formula C30H47Cl2N5O5S; molecular weight 660.70 g·mol⁻¹.
- Intended for research use; follow proper handling and storage instructions.
Medchemexpress LLC 2-Pyridinecarboxylic acid, 2-(2-pyridinyl)hydrazide | 53995-62-3 | 99.9% | 214.22 | 100 MG
PFI-90 is a selective inhibitor of histone demethylase (KDM3B) which inhibits PAX3-FOXO1 action. It induces apoptosis and myogenic differentiation, leading to increased cell death, and has potential for antitumor activity. This product is for research use only.
- Selective inhibitor of histone demethylase (KDM3B)
- Induces apoptosis and myogenic differentiation
- Exhibits dose-response in various cell lines (RH4, RH30, OSA-CL, TC-32)
- Increases apoptosis in RH4 and SCMC cells at 3 μM concentration
- Potential for antitumor activity