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95

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8

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2

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17

Biochemical Assay Reagents

5

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1

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2

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9

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Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-115451

    DNA/RNA Synthesis Others
    Photoregulin 3 (compound T4) can promote distal-to-proximal alternative polyadenylation (APA) activity in multiple transcripts .
    Photoregulin 3
  • HY-167069

    Azide-Polysarcosine100

    Biochemical Assay Reagents Others
    Azide-pSar100 (Azide-Polysarcosine100) is a pSar-lipid derivative. Azide-pSar100 is a hydrophilic alternative to PEG and can be used in drug delivery research .
    Azide-pSar100
  • HY-167067

    DSPE-Polysarcosine100

    Biochemical Assay Reagents Others
    DSPE-pSar100 (DSPE-Polysarcosine100) is a pSar-lipid derivative. DSPE-pSar100 is a hydrophilic alternative to PEG and can be used in drug delivery research .
    DSPE-pSar100
  • HY-167068

    Azide-Polysarcosine150

    Biochemical Assay Reagents Others
    Azide-pSar150 (Azide-Polysarcosine150) is a pSar-lipid derivative. Azide-pSar150 is a hydrophilic alternative to PEG and can be used in drug delivery research .
    Azide-pSar150
  • HY-167063

    Azide-Polysarcosine20

    Biochemical Assay Reagents Others
    Azide-pSar20 (Azide-Polysarcosine20) is a pSar-lipid derivative. Azide-pSar20 is a hydrophilic alternative to PEG and can be used in drug delivery research .
    Azide-pSar20
  • HY-167065

    DSPE-Polysarcosine20

    Biochemical Assay Reagents Others
    DSPE-pSar20 (DSPE-Polysarcosine20) is a pSar-lipid derivative. DSPE-pSar20 is a hydrophilic alternative to PEG and can be used in drug delivery research .
    DSPE-pSar20
  • HY-167064

    DSPE-Polysarcosine50

    Biochemical Assay Reagents Others
    DSPE-pSar50 (DSPE-Polysarcosine50) is a pSar-lipid derivative. DSPE-pSar50 is a hydrophilic alternative to PEG and can be used in drug delivery research .
    DSPE-pSar50
  • HY-167066

    DSPE-Polysarcosine150

    Biochemical Assay Reagents Others
    DSPE-pSar150 (DSPE-Polysarcosine150) is a pSar-lipid derivative. DSPE-pSar150 is a hydrophilic alternative to PEG and can be used in drug delivery research .
    DSPE-pSar150
  • HY-166972

    pSar 50

    Biochemical Assay Reagents Others
    Polysarcosine 50 (pSar 50) is a hydrophilic alternative to PEG that has good targeted drug delivery properties and can remain in the bloodstream longer. Polysarcosine 50 can be used in drug delivery research .
    Polysarcosine 50
  • HY-166973

    pSar 20

    Biochemical Assay Reagents Others
    Polysarcosine 20 (pSar 20) is a hydrophilic alternative to PEG that has good targeted drug delivery properties and can remain in the bloodstream longer. Polysarcosine 20 can be used in drug delivery research .
    Polysarcosine 20
  • HY-166974

    pSar 150

    Biochemical Assay Reagents Others
    Polysarcosine 150 (pSar 150) is a hydrophilic alternative to PEG that has good targeted drug delivery properties and can remain in the bloodstream longer. Polysarcosine 150 can be used in drug delivery research .
    Polysarcosine 150
  • HY-166975

    pSar 100

    Biochemical Assay Reagents Others
    Polysarcosine 100 (pSar 100) is a hydrophilic alternative to PEG that has good targeted drug delivery properties and can remain in the bloodstream longer. Polysarcosine 100 can be used in drug delivery research .
    Polysarcosine 100
  • HY-135562

    Antibiotic Parasite Dihydroorotate Dehydrogenase DNA/RNA Synthesis Infection Cardiovascular Disease Inflammation/Immunology Cancer
    Ascofuranone, a prenylphenol antibiotic, is a potent and selective trypanosome alternative oxidase (TAO) inhibitor. Ascofuranone has inhibitory activity against human dihydroorotate dehydrogenase (DHODH). Ascofuranone has diverse physiological activities, including antibiotic, hypolipidemic, anti-inflammatory, and anti-cancer .
    Ascofuranone
  • HY-146812

    G-quadruplex Cancer
    DIZ-3 is a selective multimeric G4 ligand based on a G4-ligand-dimerizing strategy. DIZ-3 intercalates into the G4-G4 interface, stabilizing the higher-order structure. DIZ-3 induces cell cycle arrest and apoptosis, and thus inhibits cell proliferation in alternative lengthening of telomere (ALT) cancer cells .
    DIZ-3
  • HY-101797

    (±)-Veralipride; LIR166

    Dopamine Receptor Neurological Disease
    Veralipride is a D2 receptor antagonist. It is an alternative antidopaminergic treatment for menopausal symptoms.
    Veralipride
  • HY-W010981

    Tributyl O-acetylcitrate; ATBC

    Biochemical Assay Reagents Others
    Acetyl tributyl citrate (Tributyl O-acetylcitrate; ATBC) is an alternative plasticizer .
    Acetyl tributyl citrate
  • HY-157201

    Biochemical Assay Reagents Inflammation/Immunology
    Zeo is a hapten of zearalenone with longer linkers and with alternative tethering sites have been designed for immunizing and assay conjugate preparation .
    ZEo
  • HY-111178

    BisfluoroModafinil; CRL-40940

    Drug Derivative Neurological Disease
    Lauflumide (BisfluoroModafinil) is the common alternative of modafinil. Modafinil is commonly prescribed for the research narcolepsy. Lauflumide has the potential for cognitive enhancing .
    Lauflumide
  • HY-157335

    Biochemical Assay Reagents Others
    Mn(II)-DO3A sodium is a Mn(II) complex and a potential alternative to Gd-based MRI contrast agents .
    Mn(II)-DO3A sodium
  • HY-117930
    Danicopan
    3 Publications Verification

    ACH-4471

    Complement System Inflammation/Immunology
    Danicopan (ACH-4471), a selective and orally active small-molecule factor D inhibitor, shows high binding affinity to human Factor D with Kd value of 0.54 nM. Danicopan (ACH-4471) inhibits alternative pathway of complement (APC) activity, has potential to block the alternative pathway of complement in paroxysmal nocturnal hemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS) .
    Danicopan
  • HY-131009

    PARP Others
    Fluorescein-NAD+ is an alternative to radiolabeled NAD and a substrate for ADP-ribosylation. Fluorescein-NAD+ can be used in PARP assays by fluorescence microscopy. Extinction Coefficient: 262 nm.
    Fluorescein-NAD+
  • HY-134851
    HIV-1 inhibitor-6
    1 Publications Verification

    HIV Infection
    HIV-1 inhibitor-6 (compound 9), a diheteroarylamide-based compound, is a potent HIV-1 pre-mRNA alternative splicing inhibitor. HIV-1 inhibitor-6 blocks HIV replication. HIV-1 inhibitor-6 is active against wild-type HIV-1IIIB (subtype B, X4-tropic) and HIV-1 97USSN54 (subtype A, R5-tropic) with EC50s of 0.6 μM and 0.9 μM, respectively. HIV-1 inhibitor-6 inhibits HIV strains resistant to agents targeting HIV reverse transcriptase, protease, integrase, and coreceptor CCR5 with EC50s ranging from 0.9 to 1.5 μM .
    HIV-1 inhibitor-6
  • HY-N0054
    Osthole
    Maximum Cited Publications
    11 Publications Verification

    Osthol; NSC 31868

    Histamine Receptor Apoptosis Parasite HBV Infection Cardiovascular Disease Inflammation/Immunology Endocrinology Cancer
    Osthole (Osthol) is a natural antihistamine alternative. Osthole may be a potential inhibitor of histamine H1 receptor activity. Osthole also suppresses the secretion of HBV in cells.
    Osthole
  • HY-135717

    Biochemical Assay Reagents Cancer
    Norbiotinamine is an alternative to biotin. Norbiotinamine can be coupled with a carboxylic group of amino acids to give inverse peptides, having the amide linkage oriented in the opposite direction .
    Norbiotinamine
  • HY-135717A

    Biochemical Assay Reagents Cancer
    Norbiotinamine hydrochloride is an alternative to biotin. Norbiotinamine can be coupled with a carboxylic group of amino acids to give inverse peptides, having the amide linkage oriented in the opposite direction .
    Norbiotinamine hydrochloride
  • HY-N12265

    Others Inflammation/Immunology
    Versicolactone B is a sesquiterpene that can be isolated from Viola yedoensis. Versicolactone B exhibits anti-complement activity against the classical pathway and the alternative pathway .
    Versicolactone B
  • HY-103339

    FAAH MAGL Neurological Disease
    VDM11 is a potent and selective anandamide membrane transporter (AMT) inhibitor . VDM11 inhibits FAAH and MAGL and may act as an alternative FAAH substrate .
    VDM11
  • HY-B1337C

    Biochemical Assay Reagents Endogenous Metabolite Others
    Choline (chloride), >98% serves as a pharmaceutical secondary standard for quality control, offering pharmaceutical laboratories and manufacturers a convenient and cost-effective alternative to preparing in-house working standards.
    Choline (chloride), >98%
  • HY-P99965

    SKY59; RO7112689

    Complement System Cardiovascular Disease Metabolic Disease
    Crovalimab (SKY59; RO7112689) is a novel humanized antibody against C5 in a pH-dependent manner with KDs of 15.2 nM and 16.8 μM at pH 7.4 and 5.8, respectively. Crovalimab binds human FcRn with great affinity (KD: 17 μM at pH 6.0). Crovalimab can block cleavage of C5 by the C5 convertase and inhibite the activity of a C5 variant (p.Arg885His). Crovalimab inhibits C5b-9 formation significantly in all three complement pathways, the classical pathway (CP), lectin pathway (LP), and alternative pathway (AP). Crovalimab has the potential for paroxysmal nocturnal hemoglobinuria (PNH) and complement-mediated diseases research .
    Crovalimab
  • HY-D1030

    Fluorescent Dye Inflammation/Immunology
    Fluorescein Biotin is used as an alternative to radioactive biotin for detecting and quantitating biotin-binding sites by either fluorescence or absorbance; the the fluorescence or absorbance of Fluorescein Biotin is quenched, upon binding to avidin or streptavidin.
    Fluorescein Biotin
  • HY-138650

    Glyceryl monocaprylate; Sefsol 318

    Bacterial Inflammation/Immunology
    Monocaprylin (Glyceryl monocaprylate), a monoglyceride of caprylic acid, exhibits an excellent antibacterial activity. Monocaprylin inhibits a variety of foodborne pathogenic and spoilage microorganisms and has the potential for an alternative food preservative research .
    Monocaprylin
  • HY-107915

    (-)-Cobefrin; (-)-α-Methylnoradrenaline; (-)-Nordefrin

    Adrenergic Receptor Others
    Levonordefrin, a common alternative to levoepinephrine as a vasoconstrictor in dental local agent that can suppress or relieve pain, is usually used in fivefold higher concentrations. Levonordefrin is generally considered equivalent to epinephrine .
    Levonordefrin
  • HY-P1512

    SOD Cancer
    Antioxidant peptide A is a short peptide, which contains alternative aromatic or sulfur-containing amino acid. The side chains of Antioxidant peptide A are believed to contribute to strong radical scavenging activities of peptides in the cancer cell.
    Antioxidant peptide A
  • HY-129462

    IPETC

    Others Others
    O-Isopropyl ethylthiocarbamate can be used as an environmentally friendly alternative in combination with pyrogallic acid (PGA) to replace the lime-xanthate flotation process traditionally used for chalcopyrite-molybdenite (ccp-mlb) ores .
    O-Isopropyl ethylthiocarbamate
  • HY-W010981R

    Biochemical Assay Reagents Others
    Acetyl tributyl citrate (Standard) is the analytical standard of Acetyl tributyl citrate. This product is intended for research and analytical applications. Acetyl tributyl citrate (Tributyl O-acetylcitrate; ATBC) is an alternative plasticizer .
    Acetyl tributyl citrate (Standard)
  • HY-116844

    Glidiazine

    Drug Derivative Insulin Receptor Metabolic Disease
    Glymidine (Glidiazine) is a hypoglycaemic agent. Glymidine is a lipid soluble sulphapyrimidine derivative. Glymidine appears to stimulate insulin release from pancreas. Glymidine is a possible alternative to the sulphonylureas and biguanides for the research of diabetes mellitus .
    Glymidine
  • HY-W760733

    Biochemical Assay Reagents Metabolic Disease
    2,4-Decadienal is a toxic aldehyde produced by the oxidation of linoleic acid-rich oils. 2,4-decadienal can be used as an alternative oxidation indicator for linoleic acid-rich oils .
    2,4-Decadienal
  • HY-B1817A

    Zinc(II) acetate, 99.99% trace metals basis

    Biochemical Assay Reagents Others
    Zinc acetate, 99.99% trace metals basis (Zinc(II) acetate, 99.99% trace metals basis) can be used as an alternative staining agent in SDS electrophoresis and can also affect the permeability of biological membranes.
    Zinc acetate, 99.99% trace metals basis
  • HY-169740

    Fluorescent Dye Others
    L-Luciferin is a competitive inhibitor of firefly Luciferin and can be used as an alternative substrate for light production, increasing the concentration of the enzyme or L-luciferin reduces the amount of light produced compared to D-Luciferin catalysis .
    L-Luciferin
  • HY-126395

    Fluorescent Dye Others
    Patent Blue V has been widely used in sentinel lymph node mapping. Patent Blue V is also a food coloring agent and an alternative dye for trypan blue (TB) in descemet membrane endothelial keratoplasty (DMEK) .
    Patent Blue V calcium salt
  • HY-B1657

    Drug Intermediate Neurological Disease
    Fosphenytoin is a phosphate ester proagent developed as an alternative to intravenous phenytoin for acute intervention of seizures. Fosphenytoin has advantages including more convenient and rapid intravenous administration, availability for intramuscular injection, and low potential for adverse local reactions at injection sites .
    Fosphenytoin
  • HY-148828

    iGluR Neurological Disease
    LSP-GR3 is a novel chemically-modified RNA oligonucleotides, called splice modulating oligomers (SMOs), which potently and specifically modulate GluR alternative splicing to GluR3-flip expression throughout the CNS.
    LSP-GR3
  • HY-148828A

    iGluR Neurological Disease
    LSP-GR3 sodium is a novel chemically-modified RNA oligonucleotides, called splice modulating oligomers (SMOs), which potently and specifically modulate GluR alternative splicing to GluR3-flip expression throughout the CNS.
    LSP-GR3 sodium
  • HY-109079A

    DWP14012 hydrochloride; Fexuprazan hydrochloride

    Proton Pump Metabolic Disease
    Abeprazan hydrochloride (DWP14012 hydrochloride) is a potassium-competitive acid blocker. Abeprazan hydrochloride inhibits H +, K +- ATPase by reversible potassium-competitive ionic binding with no acid activation required. Abeprazan hydrochloride is developed as a potential alternative to proton pump inhibitor for the treatment of acid-related diseases .
    Abeprazan hydrochloride
  • HY-109079

    DWP14012; Fexuprazan

    Proton Pump Metabolic Disease
    Abeprazan (DWP14012) is a potassium-competitive acid blocker. Abeprazan inhibits H +, K +- ATPase by reversible potassium-competitive ionic binding with no acid activation required. Abeprazan is developed as a potential alternative to proton pump inhibitor for the treatment of acid-related diseases .
    Abeprazan
  • HY-155639
    Tyramide alkyne
    1 Publications Verification

    Biochemical Assay Reagents Others
    Tyramide alkyne is an alternative labeling substrate that can be coupled to detection or enrichment moieties via a Copper-catalyzed Azide/Alkyne Cycloaddition (CuAAC) “click” reaction. Tyramide alkyne can be used for ascorbate peroxidase 2 (APEX2) labeling .
    Tyramide alkyne
  • HY-N0054R

    Histamine Receptor Apoptosis Parasite HBV Infection Cardiovascular Disease Inflammation/Immunology Endocrinology Cancer
    Osthole (Standard) is the analytical standard of Osthole. This product is intended for research and analytical applications. Osthole (Osthol) is a natural antihistamine alternative. Osthole may be a potential inhibitor of histamine H1 receptor activity. Osthole also suppresses the secretion of HBV in cells.
    Osthole (Standard)
  • HY-116865

    Endogenous Metabolite Endocrinology Cancer
    Equilenin is a B-ring unsaturated estrogen and one of the main ingredients in Premarin, a drug commonly used in estrogen replacement therapy. Equilenin can bind to estrogen receptors in the body and exert effects similar to endogenous estrogen. Equilenin can be used in estrogen replacement therapy and breast cancer research .
    Equilenin
  • HY-W040270

    PROTAC Linkers Cancer
    Amino-PEG10-amine, a PEG-based PROTAC linker used to combine two mono diethylstilbestrol (DES)-based ligands, provides an alternative strategy for preparing more selective and active ER antagonists for endocrine therapy of breast cancer .
    Amino-PEG10-amine
  • HY-161239

    Bacterial Antibiotic Infection
    (S)-IB-96212 (compound 4), an oligomycin derivative, inhibits the MurD2 reaction, but not the MurL reaction. (S)-IB-96212 is a specific inhibitor of the alternative pathway of peptidoglycan biosynthesis. (S)-IB-96212 weakly inhibits the MurD reaction .
    (S)-IB-96212

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