Unsubstituted Phenols
Medchemexpress LLC HY-101073 5mg Medchemexpress, Salermide CAS:1105698-15-4 Purity:>98%
Medchemexpress, HY-101073 5mg Salermide CAS:1105698-15-4 Salermide is an inhibitor of Sirt1 and Sirt2 ; can cause strong cancer-specific apoptotic cell death. 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 HY-N0125 50mg Medchemexpress, Diosmetin CAS:520-34-3 Purity:>98%
Medchemexpress, HY-N0125 50mg Diosmetin CAS:520-34-3 Diosmetin is a natural flavonoid which inhibits human CYP1A enzyme activity with an IC 50 of 40 μM in HepG2 cell. 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 HY-N0123 50mg Medchemexpress, Aloin CAS:1415-73-2 Purity:>98%
Medchemexpress, HY-N0123 50mg Aloin CAS:1415-73-2 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 HY-N0258 5mg Medchemexpress, Epimedin A1 CAS:140147-77-9 Purity:>98%
Medchemexpress, HY-N0258 5mg Epimedin A1 CAS:140147-77-9 Epimedin A1 is a flavonoid extracted from Herba Epimedii which is one of commonly used Chinese medicines. 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.
Apexbio Technology LLC Diethylstilbestrol 56-53-1 200mg
Diethylstilbestrol (56-53-1) is a small-molecule inhibitor targeting 11 -hydroxysteroid dehydrogenase type 2 (HSD11B2) and interacting with estrogen receptors It is designed to modulate hormonal signaling and cellular steroid metabolism thereby regulating processes such as apoptosis and autophagy Diethylstilbestrol exerts its biological activity primarily through the inhibition of HSD11B2 and modulation of estrogen receptor-mediated signaling In cell-based studies Diethylstilbestrol induces oxidative DNA damage and triggers apoptotic responses in spermatogonial stem cells as well as promotes autophagy in thymic cells Based on these pharmacological properties Diethylstilbestrol holds research potential in exploring estrogen receptor-mediated signaling hormone-regulated molecular events apoptosis pathways and autophagy mechanisms in vitro
Apexbio Technology LLC Tolterodine tartrate 124937-52-6 10mg
Tolterodine tartrate (CAS 124937-52-6) is the tartrate salt form of tolterodine a small molecule that acts as a competitive antagonist at muscarinic acetylcholine receptors By selectively inhibiting these receptors particularly subtypes involved in urinary bladder contraction tolterodine tartrate reduces detrusor muscle activity This mechanism underlies its utility in studies related to bladder function muscarinic receptor pharmacology and disorders characterized by overactive bladder The compound is commonly employed in preclinical and clinical research investigating the modulation of cholinergic signaling in urological and neurological contexts
Medchemexpress LLC Honokiol dichloroacetate | 1620160-42-0 | 99.1% | 488.19 g/mol | C22H18Cl4O4 | 10MG
Honokiol DCA (honokiol dichloroacetate) is a dichloroacetate analog of honokiol supplied for research use. It has been reported to inhibit growth of human prostate cancer cells in vitro and to suppress androgen receptor (AR) protein levels, and is commonly used in cellular and mechanistic studies.
- Dichloroacetate analog of honokiol.
- Reported to inhibit prostate cancer cell growth in vitro.
- Suppresses androgen receptor protein levels.
- Available as mg-scale solids and as 10 mM solution in DMSO.
- High purity (about 99.1%).
- Molecular weight 488.19 g/mol; formula C22H18Cl4O4.
- For research use only; not for clinical use.
Medchemexpress LLC Dy131 (GSK 9089) | 95167-41-2 | C18H21N3O2 | 5 MG
DY131 (GSK 9089) is a potent and selective ERRγ and ERRβ agonist. It is inactive against ERRα, ERα, and ERβ, and also inhibits Smo signaling.
- Potent and selective ERRγ and ERRβ agonist
- Inactive against ERRα, ERα, and ERβ
- Inhibits smo signaling
- Suppresses cell proliferation in LNCaP-ERRγ and LNCaP cells
- Inhibits Shh induced accumulation of Smo::EGFP
- Decreases phosphorylated histone H3 (pH3) marked proliferation of CGNPs
Selleck Chemical LLC LY2510924
LY2510924 is a potent and selective CXCR4 antagonist that specifically blocks SDF-1 binding to CXCR4 with IC50 value of 0 079 nmol/L and inhibits SDF-1-induced GTP binding with Kb value of 0 38 nmol/L
![Medchemexpress LLC 3-[2,4-diamino-7-(3-hydroxyphenyl)pteridin-6-yl]phenol | 677297-51-7 | 99.4% | 346.34 g/mol | C18H14N6O2 | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000213113.png-250.jpg)
Medchemexpress LLC 3-[2,4-diamino-7-(3-hydroxyphenyl)pteridin-6-yl]phenol | 677297-51-7 | 99.4% | 346.34 g/mol | C18H14N6O2 | 10 MG
TG100-115 is a selective small-molecule inhibitor of PI3Kγ and PI3Kδ with nanomolar potency (IC50 83 nM and 235 nM, respectively). It is used in biochemical, cellular, and in vivo studies to investigate PI3Kγ/δ-mediated signaling, inflammatory responses, and cardioprotective effects.
- Selective inhibition of PI3Kγ and PI3Kδ.
- Nanomolar potency: PI3Kγ 83 nM, PI3Kδ 235 nM.
- Limited activity against PI3Kα and PI3Kβ (>1 μM).
- High purity (99.41%).
- Molecular weight 346.34 g/mol; formula C18H14N6O2.
- Soluble in DMSO (33.33 mg/mL) with warming and pH adjustment.
- Recommended storage: powder -20°C (3 years) or 4°C (2 years).