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ASIC1,neutral pH

" in MedChemExpress (MCE) Product Catalog:

645

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2

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111

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123

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36

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4

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1

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Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-B1610N
    Sodium Citrate Buffer, 0.1M, pH 4.0
    1 Publications Verification

    Biochemical Assay Reagents Others
    Sodium citrate buffer, 0.1M, pH 4.0, is a commonly used buffer with main components are citric acid and sodium hydrogen phosphate. Sodium citrate buffer, 0.1M, pH 4.0 is used in heat induced epitope retrieval (HIER) methods to reverse the loss of antigenicity that occurs with some epitopes in formalin-fixed paraffin embedded tissues. Sodium citrate buffer, 0.1M, pH 4.0 is the preferred solution for most antibodies [1]. Sodium citrate buffer, 0.1M, pH 4.0 is used in the hydration of liposome film .
    Sodium Citrate Buffer, 0.1M, pH 4.0
  • HY-B1610J

    Biochemical Assay Reagents Others
    Sodium citrate buffer, 0.5M, pH 5.0, is a commonly used buffer with main components are citric acid and sodium hydrogen phosphate. Sodium citrate buffer, 0.5M, pH 5.0 is used in heat induced epitope retrieval (HIER) methods to reverse the loss of antigenicity that occurs with some epitopes in formalin-fixed paraffin embedded tissues. Sodium citrate buffer, 0.5M, pH 5.0 is the preferred solution for most antibodies [1]. Sodium citrate buffer, 0.5M, pH 5.0 is used as solution for captisol in animal tumor models .
    Sodium Citrate Buffer, 0.5M, pH 5.0
  • HY-144121

    Bacterial Fungal Apoptosis Infection Cancer
    Ph-Ph+ is a hemiprotonic compound, which is produced from phenanthroline (ph) dimerization. Ph-Ph+ has antitumor, antibacterial and antifungal activities [1].
    Ph-Ph+
  • HY-B1610K

    Biochemical Assay Reagents Others
    Sodium citrate buffer, 0.5M, pH 5.5, is a commonly used buffer with main components are citric acid and sodium hydrogen phosphate. Sodium citrate buffer 0.5M pH 5.5 is used in heat induced epitope retrieval (HIER) methods to reverse the loss of antigenicity that occurs with some epitopes in formalin-fixed paraffin embedded tissues. Sodium citrate buffer 0.5M pH 5.5 is the preferred solution for most antibodies. [1].
    Sodium Citrate Buffer, 0.5M, pH 5.5
  • HY-B1610M

    Biochemical Assay Reagents Others
    Sodium citrate buffer, 0.5M, pH 6.5, is a commonly used buffer with main components are citric acid and sodium hydrogen phosphate. Sodium citrate buffer, 0.5M, pH 6.5 is used in heat induced epitope retrieval (HIER) methods to reverse the loss of antigenicity that occurs with some epitopes in formalin-fixed paraffin embedded tissues. Sodium citrate buffer, 0.5M, pH 6.5 is the preferred solution for most antibodies [1].
    Sodium Citrate Buffer, 0.5M, pH 6.5
  • HY-B1610L

    Biochemical Assay Reagents Others
    Sodium citrate buffer, 0.5M, pH 6.0, is a commonly used buffer with main components are citric acid and sodium hydrogen phosphate. Sodium citrate buffer, 0.5M, pH 6.0 is used for RNA isolation and antigens detection in fixed tissue [1].
    Sodium Citrate Buffer, 0.5M, pH 6.0
  • HY-B0246S3

    CBZ-(pH)d8; NSC 169864-(pH)d8

    Isotope-Labeled Compounds Neurological Disease Cancer
    Carbamazepine-(Ph)d8 (CBZ-(Ph)d8; NSC 169864-(Ph)d8) is the deuterium labeled Carbamazepine-(Ph) (HY-B0246) [1].
    Carbamazepine-(Ph)d8
  • HY-133463

    PROTAC Linkers Cancer
    Tetrazine-Ph-PEG5-Ph-tetrazine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs [1]. Tetrazine-Ph-PEG5-Ph-tetrazine is a click chemistry reagent, it contains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups.
    Tetrazine-Ph-PEG5-Ph-tetrazine
  • HY-133465

    PROTAC Linkers Cancer
    Tetrazine-Ph-PEG4-Ph-aldehyde is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs [1]. Tetrazine-Ph-PEG4-Ph-aldehyde is a click chemistry reagent, it contains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups.
    Tetrazine-Ph-PEG4-Ph-aldehyde
  • HY-151797

    CaMK Neurological Disease
    Ph-HTBA is a high-affinity, brain-penetrating modulator for CaMKIIα. Ph-HTBA has binding affinity for CaMKIIα with a Kd value of 757 nM. Ph-HTBA can be used for the research of ischemia and neurodegenerative disorders [1].
    Ph-HTBA
  • HY-112798

    Apolipoprotein Neurological Disease
    PH-002 is an inhibitor of apolipoprotein (apo) E4 intramolecular domain interaction in neuronal cells that could rescue impairments of mitochondrial motility and neurite outgrowth.
    PH-002
  • HY-141808

    Others Cancer
    AZD-CO-Ph-PEG4-Ph-CO-AZD is a bis-β-lactam linker can be used for antibody-siRNA conjugate synthesis [1].
    AZD-CO-Ph-PEG4-Ph-CO-AZD
  • HY-10499
    PH-064
    1 Publications Verification

    BIM-46187

    Others Neurological Disease
    PH-064 (BIM-46187) is an inhibitor of heterotrimeric G-protein complex.
    PH-064
  • HY-149669

    PI3K HDAC Apoptosis Cancer
    PH14 is a dual PI3K/HDAC inhibitor with IC50 values of 20.3 nM and 24.5 nM for PI3Kα and HDAC3, respectively. PH14 has antiproliferative activity and also induces apoptosis in Jeko-1 cells. PH14 can be used in cancer research, such as lymphoma [1].
    PH14
  • HY-140349

    PROTAC Linkers Cancer
    AZD-CO-C2-Ph-amido-Ph-azide is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs [1]. AZD-CO-C2-Ph-amido-Ph-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
    AZD-CO-C2-Ph-amido-Ph-azide
  • HY-124480

    PROTAC Linkers Cancer
    Tetrazine-Ph-acid is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs [1]. Tetrazine-Ph-acid is a click chemistry reagent, it contains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups.
    Tetrazine-Ph-acid
  • HY-D1094

    SNARF 1

    Fluorescent Dye Others
    Carboxy-SNARF 1 (5/6-mixture) (SNARF 1) is a fluorescent probe that is sensitive to pH. Carboxy-SNARF 1 (5/6-mixture) can be used for measurement pH [1].
    Carboxy-SNARF 1 (5/6-mixture)
  • HY-10499A

    BIM-46187 tetrahydrochloride

    Others Neurological Disease
    PH-064 tetrahydrochloride is an inhibitor of heterotrimeric G-protein complex.
    PH-064 (tetra(hydrochloride))
  • HY-10403A

    p38 MAPK Inflammation/Immunology
    (aS)-PH-797804 is a selective p38 MAPK inhibitor with IC50 values for p38 α /β of 26 nM and 102 nM, respectively. (aS)-PH-797804 has anti-inflammatory activity [1] .
    (aS)-PH-797804
  • HY-10403
    PH-797804
    5+ Cited Publications

    p38 MAPK Autophagy Inflammation/Immunology Cancer
    PH-797804 is a ATP-competitive, selective p38α/p38β inhibitor (IC50=26 nM and Ki=5.8 nM for p38α; Ki=40 nM for p38β) and does not inhibit JNK2.
    PH-797804
  • HY-141894

    Histone Acetyltransferase Metabolic Disease
    5-Ph-IAA-AM is an eggshell-permeable 5-Ph-IAA (HY-134653) analog which contains an acetoxymethyl (AM) group. 5-Ph-IAA-AM affords an enhanced protein degradation in laid embryos. 5-Ph-IAA-AM can be used to disclosure the roles of proteins in C. elegans, in particular those that are involved in embryogenesis and development, through temporally controlled protein degradation [1] .
    5-Ph-IAA-AM
  • HY-D1093

    Fluorescent Dye Others
    Carboxy SNARF-1, acetoxymethyl ester (5/6-mixture) is a fluorescent probe that is sensitive to pH. Carboxy SNARF-1, acetoxymethyl ester (5/6-mixture) can be used for measurement of intracellular pH [1].
    Carboxy SNARF-1, acetoxymethyl ester (5/6-mixture)
  • HY-130107

    ADC Linker Cancer
    Ald-Ph-NHS ester is a nonclaevable linker for antibody-agent-conjugation (ADC).
    Ald-Ph-NHS ester
  • HY-126908

    PROTAC Linkers Cancer
    Tetrazine-Ph-NHS ester is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs [1]. Tetrazine-Ph-NHS ester is a click chemistry reagent, it contains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups.
    Tetrazine-Ph-NHS ester
  • HY-130283

    PROTAC Linkers Cancer
    Methyltetrazine-Ph-NHS ester is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs [1]. Methyltetrazine-Ph-NHS ester is a click chemistry reagent, it contains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups.
    Methyltetrazine-Ph-NHS ester
  • HY-130928

    ADC Linker Cancer
    Tetrazine-Ph-OPSS is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) [1]. Tetrazine-Ph-OPSS is a click chemistry reagent, it contains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups.
    Tetrazine-Ph-OPSS
  • HY-D1457

    Fluorescent Dye Others
    DND-189, a low-pH fluorescent probe, is sensitive to neutral and low pH range. DND-189 can be used to measure the pH of acidic organelles [1] .
    DND-189
  • HY-D0265

    Fluorescent Dye Others
    Thymolphthalein is an electrochemically active dye due to the presence of thymol fragments. Thymolphthalein is a Phthalein dye used as an acid-base indicator. It is colourless in acid pH and is blue in basic pH [1].
    Thymolphthalein
  • HY-116497

    Others Cancer
    PH11 is a novel focal adhesion kinase (FAK) inhibitor that rapidly induces apoptosis in TRAIL-resistant PANC-1 cells when combined with TRAIL, but has no effect on normal human fibroblasts. The study found that PH11 downregulates c-FLIP through inhibition of FAK and phosphatidylinositol-3-kinase (PI3K)/AKT pathways, thereby restoring the TRAIL apoptotic pathway, suggesting that this combination therapy may provide an attractive therapeutic strategy for the safe and effective treatment of pancreatic cancer. PH11 selectively inhibits c-FLIP expression by modulating upstream signaling pathways and may represent an innovative therapeutic strategy. Although further work is needed to fully elucidate the mechanism of PH11-induced TRAIL sensitization, we believe that our results will provide a new approach to target c-FLIP without the risk of interfering with caspase-8 processing, which could potentially lead to TRAIL resistance. This study also suggests a role for the FAK/AKT signaling pathway in regulating c-FLIP expression in TRAIL-induced apoptosis, and this understanding will provide important clues to control the resistance mechanism to optimize the potential of TRAIL-based pancreatic cancer treatment.
    PH11
  • HY-W096158

    PROTAC Linkers Cancer
    Ph-PEG3 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs [1].
    Ph-PEG3
  • HY-147118

    ADC Linker Cancer
    NHS-SS-Ph is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) [1].
    NHS-SS-Ph
  • HY-153395

    Drug-Linker Conjugates for ADC Cancer
    PH-HG-005-5 (compound 16c) is a derivative of SN-38 (HY-13704) and can be used as Drug-Linker Conjugates for ADC. PH-HG-005-5 can conjugate to targeting peptides for ADCs synthesis [1].
    PH-HG-005-5
  • HY-D0252

    Fluorescent Dye Others
    m-Cresol purple is a pH indicator dye with large cross section and halochromic property in neutral pH range [1].
    m-Cresol purple
  • HY-134653
    5-Ph-IAA
    15+ Cited Publications

    Epigenetic Reader Domain Cancer
    5-Ph-IAA is a derivative of IAA. 5-Ph-IAA, a ligand, establishes the auxin-inducible degron 2 (AID2) system together with an OsTIR1 (F74G) mutant. AID2 induces rapid and efficient depletion of mAID-fused proteins to study protein function in living cells, causing tumor suppression [1].
    5-Ph-IAA
  • HY-133504

    ADC Linker Cancer
    Tetrazine-Ph-SS-amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) [1]. Tetrazine-Ph-SS-amine is a click chemistry reagent, it contains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups.
    Tetrazine-Ph-SS-amine
  • HY-Y0699

    Fluorescent Dye Others
    Methyl red is an azo dye that acts as a pH indicator. Methyl red is red and yellow at pH 4.4 and 6.0 respectively [1].
    Methyl red
  • HY-130496

    PROTAC Linkers Cancer
    Ald-Ph-PEG6-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs [1].
    Ald-Ph-PEG6-acid
  • HY-163146

    Fluorescent Dye Cancer
    TME-HYM (PH Probe) is a novel fluorescent probe based on acidic tumor microenvironment (TME) activation and organic anion transporting polypeptide (OATPs, overexpressed on cancer cells), and can be selective uptaken. TME-HYM (PH Probe) can selectively lit up cancer cells and tumor tissues, offering dual tumor selectivity for precise visualization of tumor mass [1].
    TME-HYM (PH Probe)
  • HY-D0219A

    Fluorescent Dye Others
    Thymol Blue sodium is an acid-base indicator used to indicate changes in pH. Thymol Blue sodium fades from red to yellow at pH 1.2 to 2.8 and from yellow to blue at pH 8.0 to 9.6 [1].
    Thymol Blue sodium
  • HY-159575

    PROTAC Linkers Cancer
    COOEt-cyclohexane-C-Ph-pyrimidine-diazabicyclo is a PROTAC linker. COOEt-cyclohexane-C-Ph-pyrimidine-diazabicyclo can be used in the synthesis of PROTAC SMARCA2/4-degrader-5 (HY-159456) [1].
    COOEt-cyclohexane-C-Ph-pyrimidine-diazabicyclo
  • HY-168203

    E3 Ligase Ligand-Linker Conjugates Cancer
    Thalidomide-piperidine-O-Ph-NH2 is the conjugate of E3 ligase and linker. Thalidomide-piperidine-O-Ph-NH2 can be used for synthesis of PROTAC degrader MJP6412 (HY-168201) [1].
    Thalidomide-piperidine-O-Ph-NH2
  • HY-130099

    ADC Linker Cancer
    Ald-Ph-amido-PEG2 is a noncleavable ADC linker for antibody-drug conjugate [1].
    Ald-Ph-amido-PEG2
  • HY-160113

    Biochemical Assay Reagents Others
    Sodium phosphate buffer (pH 6.9 0.02 mol/l) is a water-based salt solution. Sodium phosphate buffer (pH 6.9 0.02 mol/l) can be used in a variety of biochemical studies.
    Sodium phosphate buffer (pH 6.9 0.02 mol/l)
  • HY-D0219

    ThymolsulpHonepHthalein

    Fluorescent Dye Others
    Thymol Blue sodium is an acid-base indicator used to indicate changes in pH. Thymol Blue sodium fades from red to yellow at pH 1.2 to 2.8 and from yellow to blue at pH 8.0 to 9.6 [1]. Storage: protect from light.
    Thymol blue
  • HY-130846

    PROTAC Linkers Cancer
    Pip-alkyne-Ph-COOCH3 is an alkyl chain-based PROTAC linker can be used in the synthesis of PROTAC ARD-266 [1]. Pip-alkyne-Ph-COOCH3 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    Pip-alkyne-Ph-COOCH3
  • HY-130551

    PROTAC Linkers Cancer
    Tetrazine-Ph-PEG5-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs [1]. Tetrazine-Ph-PEG5-NHS ester is a click chemistry reagent, it contains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups.
    Tetrazine-Ph-PEG5-NHS ester
  • HY-W579346

    Biochemical Assay Reagents Others
    POPSO sesquisodium is a water-soluble zwitterionic buffer. POPSO sesquisodium is commonly used in biological and biochemical studies to maintain the acidity or alkalinity (pH value) of solutions, especially within the physiological pH range of 7.0 to 8.5 [1].
    POPSO sesquisodium
  • HY-169365

    PD-1/PD-L1 Others
    2-Methylbiphenyl-oxadiazole-NH-Ph-CHO is the PD-L1 ligand part of AUTAC PD-L1 degrader-3 (HY-169363). 2-Methylbiphenyl-oxadiazole-NH-Ph-CHO can be utilized in AUTAC synthesis [1].
    2-Methylbiphenyl-oxadiazole-NH-Ph-CHO
  • HY-126524

    ADC Linker Cancer
    N3-Ph-NHS ester is a noncleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). N3-Ph-NHS ester is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
    N3-Ph-NHS ester
  • HY-168217

    E3 Ligase Ligand-Linker Conjugates Cancer
    Thalidomide-piperazine-piperidine-2-F-Ph-CHO is a E3 ligase ligand-linker conjugate, which is consisted of a Thalidomide (HY-14658) and a linker Boc-Piperazine-piperidine-2-F-Ph-CHO (HY-168218). Thalidomide-piperazine-piperidine-2-F-Ph-CHO is utilized for synthesis of PROTAC molecule YDR1 (HY-168215) [1].
    Thalidomide-piperazine-piperidine-2-F-Ph-CHO

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