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Results for "

traveler’s diarrhea

" in MedChemExpress (MCE) Product Catalog:

9509

Inhibitors & Agonists

34

Screening Libraries

76

Fluorescent Dye

230

Biochemical Assay Reagents

559

Peptides

6

MCE Kits

118

Inhibitory Antibodies

1069

Natural
Products

594

Recombinant Proteins

720

Isotope-Labeled Compounds

229

Antibodies

120

Click Chemistry

168

Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-W420033
    (S)-(+)-Etomoxir

    		Acyltransferase Others
    (S)-(+)-Etomoxir is the S enantiomer of Etomoxir (HY-50202). Etomoxir is an irreversible inhibitor of carnitine palmitoyltransferase 1a (CPT-1a), inhibits fatty acid oxidation (FAO) through CPT-1a and inhibits palmitate β-oxidation in human, rat and guinea pig .
    (S)-(+)-Etomoxir
  • HY-B0102B
    (S)-Fluoxetine hydrochloride

    		Serotonin Transporter Neurological Disease
    (S)-Fluoxetine hydrochloride, an antidepressant, is serotonin reuptake inhibitor (SSRI) .
    (S)-Fluoxetine hydrochloride
  • HY-154659
    Polycarbophil

    		Biochemical Assay Reagents Others
    Polycarbophil is an orally active hydrophilic polymer. Polycarbophil achieves bioadhesion through hydrogen bonding between carboxyl groups and mucosal surfaces, and prolongs compound retention time and regulates compound release through swelling properties. Polycarbophil relieves constipation and diarrhea .
    Polycarbophil
  • HY-P5077A
    Guanylin (mouse, rat) (TFA)

    		Guanylate Cyclase Metabolic Disease
    Guanylin (mouse, rat) TFA, a petide, is composed of 15 amino acids. Guanylin (mouse, rat) TFA is an activator of intestinal guanylate cyclase. Guanylin (mouse, rat) TFA can be used for the research of diarrhea .
    Guanylin (mouse, rat) (TFA)
  • HY-155228
    LK-44

    		Others Inflammation/Immunology
    hCES2A-IN-2 (Compound 44) is an orally active human carboxylesterase 2 (hCES2A) inhibitor (IC50: 5.02 μM). hCES2A-IN-2 improves Irinotecan (HY-16562)-induced delayed diarrhea .
    LK-44
  • HY-B0519C
    Tylosin lactate

    		Bacterial Infection
    Tylosin (lactate) is an anti-bacterial agent that can target spore-forming bacteria. Tylosin (lactate) can increase the levels of Enterococcus and lactobacilli in dogs' feces and help relieve tylosin-responsive diarrhea .
    Tylosin lactate
  • HY-176465
    hCES2A-IN-3

    		Carboxylesterase (CES) Inflammation/Immunology
    hCES2A-IN-3 (Compound 9d) is a potent serine-targeting covalent human carboxylesterase 2A (hCES2A) inhibitor with an IC50 value of 0.12 nM. hCES2A-IN-3 is promising for research of diarrhea and ulcerative colitis .
    hCES2A-IN-3
  • HY-P5077
    Guanylin (mouse, rat)

    		Guanylate Cyclase Metabolic Disease
    Guanylin (mouse, rat), a petide, is composed of 15 amino acids. Guanylin (mouse, rat) is an activator of intestinal guanylate cyclase. Guanylin (mouse, rat) can be used for the research of diarrhea .
    Guanylin (mouse, rat)
  • HY-P4521
    Ac-Pro-Leu-Gly-[(S)-2-mercapto-4-methyl-pentanoyl]-Leu-Gly-OEt

    		MMP Others
    Ac-Pro-Leu-Gly-[(S)-2-mercapto-4-methyl-pentanoyl]-Leu-Gly-OEt is a MMP12 substrate, and can be used to detect MMP12 enzyme activity .
    Ac-Pro-Leu-Gly-[(S)-2-mercapto-4-methyl-pentanoyl]-Leu-Gly-OEt
  • HY-149802
    SLC26A3-IN-1

    		GLUT Metabolic Disease
    SLC26A3-IN-1 is an inhibitor of anion exchanger protein SLC26A3 (IC50=340 nM). SLC26A3 belongs to solute carrier (SLC) proteins, and the SLC26 family. SLC26 family has broad anion specificity for chloride, bicarbonate, sulfate and oxalate. SLC26A3 down-regulates in adenoma, DRA, involves in in intestinal absorption of chloride and oxalate. The loss of SLC26A3 function mutations is associated with chloride-losing diarrhea .
    SLC26A3-IN-1
  • HY-149276
    SLC26A3-IN-2
    1 Publications Verification

    		 GLUT Metabolic Disease
    SLC26A3-IN-2 is an orally active inhibitor of anion exchanger protein SLC26A3 (IC50=360 nM). SLC26A3 belongs to solute carrier (SLC) proteins, and the SLC26 family. SLC26 family has broad anion specificity for chloride, bicarbonate, sulfate and oxalate. SLC26A3 down-regulates in adenoma, DRA, involves in in intestinal absorption of chloride and oxalate. The loss of SLC26A3 function mutations is associated with chloride-losing diarrhea .
    SLC26A3-IN-2
  • HY-P990387
    Anti-CTSS/Cathepsin S Antibody (Fsn0503h)

    		Ser/Thr Protease Inflammation/Immunology
    The Anti-CTSS/Cathepsin S Antibody (Fsn0503h) is a humanized antibody expressed in CHO cells, targeting CTSS/Cathepsin S. The Anti-CTSS/Cathepsin S Antibody (Fsn0503h) has a huIgG1 type heavy chain and a huκ type light chain, with a predicted molecular weight (MW) of 150 kDa. The isotype control for Anti-CTSS/Cathepsin S Antibody (Fsn0503h) can be referenced as Human IgG1 kappa, Isotype Control (HY-P99001).
    Anti-CTSS/Cathepsin S Antibody (Fsn0503h)
  • HY-E70226
    Cathepsin S, human

    CTSS

    		 Ser/Thr Protease Cardiovascular Disease Inflammation/Immunology Cancer
    Cathepsin S, human, is a potent cysteine protease that promotes the degradation of damaged or harmful proteins in the endolysosomal pathway. Cathepsin S, human, is involved in multiple pathological processes, including arthritis, cancer, and cardiovascular disease .
    Cathepsin S, human
  • HY-132593
    Rovanersen

    WVE-120101

    		 Huntingtin Neurological Disease
    Rovanersen (WVE-120101) is an antisense oligonucleotide that specifically targets mutated mRNA copies of the huntington (HTT) gene without affecting healthy mRNA of HTT gene, thereby preventing the production of faulty Huntingtin protein. Rovanersen can be used for huntington’s disease research .
    Rovanersen
  • HY-155181
    hCES2-IN-1

    		Others Cancer
    hCES2-IN-1 (Compound 24) is a reversible and selective hCES2 inhibitor (IC50: 6.72 μM). hCES2-IN-1 reduces the level of hCES2 in living cells. hCES2-IN-1 is effective against Irinotecan (HY-16562)-induced delayed diarrhea and DSS-induced ulcerative colitis .
    hCES2-IN-1
  • HY-131976
    BVDV-IN-1

    		Flavivirus Infection
    BVDV-IN-1 is a non-nucleoside inhibitor (NNI) of bovine viral diarrhea virus (BVDV), with an EC50 of 1.8 μM. BVDV-IN-1 directly binds to a hydrophobic pocket of the BVDV RdRp. BVDV-IN-1 has antiviral activity against BVDV resistant to NNI thiosemicarbazone (TSC) .
    BVDV-IN-1
  • HY-107547
    BPIPP

    		Guanylate Cyclase Adenylate Cyclase Metabolic Disease
    BPIPP is a guanylyl cyclase type C (GC-C) and adenylyl cyclase inhibitor that can suppress cyclic nucleotide synthesis. BPIPP inhibits chloride-ion transport stimulated by activation of guanylyl or adenylyl cyclases, and has the potential for diarrhea research .
    BPIPP
  • HY-A0274
    Ramosetron

    YM060 free base

    		 5-HT Receptor Others
    Ramosetron (YM060 free base) is an orally active 5-HT3 antagonist that improves dysphoria, interference with activity and food avoidance. Ramosetron is promising for research of irritable bowel syndrome with diarrhea .
    Ramosetron
  • HY-401913
    endo CNTinh-03

    		Phosphodiesterase (PDE) Infection Cancer
    Endo CNTinh-03 is inhibitor for the elevation of cAMP and cGMP induced by agonist, such as G protein-coupled receptors, adenylate cyclase, and guanylate cyclase (IC50 is 4 μM). Endo CNTinh-03 inhibits cholera toxin- and Escherichia coli (STa) toxin- induced CFTR chloride current, ameliorates secretory diarrhea in mouse models, and prevents cyst growth in polycystic kidney disease model .
    endo CNTinh-03
  • HY-N5142
    α-Terpineol

    		Bacterial Antibiotic NF-κB AMPK Fungal Infection Neurological Disease Metabolic Disease Inflammation/Immunology
    α-Terpineol (with oral activity) can be found in Eucalyptus globulus Labill. α-Terpineol exhibits strong antimicrobial activity against periodontopathic and cariogenic bacteria.α-Terpineol possesses antifungal activity against T. mentagrophytes, and the activity might lead to irreversible cellular disruption. In addition, α-Terpineol exhibits antineuropathic and anti-inflammatory activities. α-Terpineol can be utilized in research related to diarrhea, neuropathic pain, infections, and inflammation .
    α-Terpineol
  • HY-126732
    L-640876

    		Antibiotic Bacterial Infection
    L-640876 is a broad-spectrum and orally active lactam antimicrobial agent. L-640876 showa MIC90 of 0.125 pg/mL for the E. coli strains, 2 /mg/mL for the S.choleraerai strains and 4 pg/mL for the S. typhinwrium strains .
    L-640876
  • HY-125845A
    (S,S,S)-AHPC hydrochloride
    2 Publications Verification

    (S,S,S)-VH032-NH2 hydrochloride

    		 Ligands for E3 Ligase Cancer
    (S,S,S)-AHPC hydrochloride is a von Hippel-Lindau (VHL) amino building block. (S,S,S)-AHPC (Compound 27) is a ligand used as a negative control for (S,R,S)-AHPC. (S,R,S)-AHPC is the VH032-based VHL ligand used in the recruitment of the VHL protein .
    (S,S,S)-AHPC hydrochloride
  • HY-119813
    (S,S)-Sinogliatin

    (S,S)-HMS-5552; (S,S)-RO-5305552

    		 Glucokinase Metabolic Disease
    (S,S)-Sinogliatin ((S,S)-HMS-5552) is the (S,S) -enantiomer of Sinogliatin. Sinogliatin is a glucokinase activator that can be used to study type 2 diabetes .
    (S,S)-Sinogliatin
  • HY-17518A
    (S,S)-Valifenalate

    (S,S)-IR5885; (S,S)-Valiphenal

    		 Fungal Infection
    (S,S)-Valifenalate ((S,S)-IR5885) is an acylamino acid fungicide and is used to control a wide range of fungi belonging to the class of Oomycetes. (S,S)-Valifenalate ((S,S)-IR5885) interferes with the cell-wall synthesis thus affecting the growth stages of the pathogens controlled, both outside (on the spores) or inside the plant (on the mycelium) .
    (S,S)-Valifenalate
  • HY-123109A
    (S,S,S)-AHPC-Boc

    (S,S,S)-VH032-Boc

    		 Ligands for E3 Ligase Cancer
    (S,S,S)-AHPC-Boc is the isomer of (S,R,S)-AHPC-Boc (HY-123109), and can be used as an experimental control. (S,R,S)-AHPC-Boc (VH032-Boc) is a ligand used in the recruitment of the von Hippel-Lindau (VHL) protein. (S,R,S)-AHPC-Boc is used in PROTAC technology .
    (S,S,S)-AHPC-Boc
  • HY-172298
    (R,S,S,S)-Orlistat

    (R,S,S,S)-Tetrahydrolipstatin; (R,S,S,S)-Ro-18-0647

    		 Fatty Acid Synthase (FASN) Infection
    (R,S,S,S)-Orlistat is a stereogenic derivative of orlistat (tetrahydrolipstatin; THL) (HY-B0218). (R,S,S,S)-Orlistat inhibits three Mycobacterium tuberculosis lipid esterases, Ag85C (KI: 16.43 μM), Rv3802 (EC50: 16.2 nM), and Pks13-TE .
    (R,S,S,S)-Orlistat
  • HY-107409B
    (S,S)-GNE 5729

    		Drug Isomer Others
    (S,S)-GNE 5729 is a (S,S)-enantiomer of GNE 5729 (HY-107409) .
    (S,S)-GNE 5729
  • HY-16776A
    (2S,5S)-Censavudine

    (2S,5S)-Festinavir; (2S,5S)-BMS-986001; (2S,5S)-OBP-601

    		 HIV Infection
    (2S,5S)-Censavudine ((2S,5S)-OBP-601) is the (2S,5S)-enantiomer of Censavudine. Censavudine, a nucleoside reverse transcriptase inhibitor, is a potent HIV inhibitor . (2S,5S)-Censavudine is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    (2S,5S)-Censavudine
  • HY-145543
    9(S)10(S)13(S)-TriHOME

    		Biochemical Assay Reagents Metabolic Disease
    9(S)10(S)13(S)-TriHOME is an ester product.
    9(S)10(S)13(S)-TriHOME
  • HY-107608A
    5(S),12(S)-Leukotriene B4

    5(S),12(S)-LTB4; 5(S),12(S)-DiHETE

    		 Drug Isomer Others
    5(S),12(S)-Leukotriene B4 (5(S),12(S)-LTB4; 5(S),12(S)-DiHETE) is a stereochemical isomer of LTB4 (HY-107608) .
    5(S),12(S)-Leukotriene B4
  • HY-N0894B
    (3S,5S)-Octahydrocurcumin

    (3S,5S)-Hexahydrobisdemethoxycurcumin

    		 Drug Metabolite Infection
    (3S,5S)-Octahydrocurcumin ((3S,5S)-Hexahydrobisdemethoxycurcumin) is a fungal metabolite that can be isolated from Curcuma longa .
    (3S,5S)-Octahydrocurcumin
  • HY-128888A
    (S,S)-GSK321

    		Isocitrate Dehydrogenase (IDH) Cancer
    (S,S)-GSK321 is a (S,S)-enantiomer of GSK321 .
    (S,S)-GSK321
  • HY-W681822
    (R,S,S)-Dihydrotetrabenazine

    R,S,S-DHTBZ

    		 Drug Metabolite Monoamine Transporter Neurological Disease
    (R,S,S)-Dihydrotetrabenazine (R,S,S-DHTBZ) is a kind of discrete isomeric secondary alcohol metabolites of Tetrabenazine (TBZ, HY-B0590), is a poor VMAT2 inhibitor (Ki = 690 nM) .
    (R,S,S)-Dihydrotetrabenazine
  • HY-B0010C
    (S,S)-Formoterol

    (+)-Formoterol

    		 Interleukin Related Inflammation/Immunology
    (S,S)-Formoterol ((+)-Formoterol) is a (S,S)-enantiomer of Formoterol. (S,S)-Formoterol can promote asthma by enhancing IL-4 production in mast cells of the asthmatic airway .
    (S,S)-Formoterol
  • HY-167739
    (S,S)-Dehydroemetine

    		Endogenous Metabolite Neurological Disease
    (S,S)-Dehydroemetine is an antispasmodic compound with inhibitory activity on smooth muscle. (S,S)-Dehydroemetine can be used to inhibit diseases related to smooth muscle contraction .
    (S,S)-Dehydroemetine
  • HY-149154
    (4S,5S,6S,12aS)-Oxytetracycline

    		Antibiotic Infection
    (4S,5S,6S,12aS)-Oxytetracycline is a broad-spectrum antibiotic that can inhibit the synthesis of protein in bacteria. (4S,5S,6S,12aS)-Oxytetracycline is an important member of the bacterial aromatic polyketone family, a type of natural product with diverse structures .
    (4S,5S,6S,12aS)-Oxytetracycline
  • HY-168398
    9(S),12(S),13(S)-TriHODE

    		Drug Derivative Cancer
    9(S),12(S),13(S)-TriHODE is an α-Linolenic acid (HY-N0728)-derived oxylipin that has been found in C. olitorius .
    9(S),12(S),13(S)-TriHODE
  • HY-112403
    (S)-Roscovitine

    (S)-Seliciclib; (S)-CYC202

    		 CDK Neurological Disease
    (S)-Roscovitine ((S)-Seliciclib; (S)-CYC202) is a potent and cross the blood-brain barrier CDKs inhibitor. (S)-Roscovitine shows neuroprotective efficacy. (S)-Roscovitine has the potential for the research of stroke .
    (S)-Roscovitine
  • HY-105099
    Rifalazil

    KRM-1648; ABI-1648

    		 Antibiotic DNA/RNA Synthesis Bacterial Infection Inflammation/Immunology
    Rifalazil (KRM-1648; ABI-1648), a rifamycin derivative, inhibits the bacterial DNA-dependent RNA polymerase and kills bacterial cells by blocking off the β-subunit in RNA polymerase . Rifalazil (KRM-1648; ABI-1648) is an antibiotic, exhibits high potency against mycobacteria, gram-positive bacteria, Helicobacter pylori, C. pneumoniae and C. trachomatis with MIC values from 0.00025 to 0.0025 μg/ml . Rifalazil (KRM-1648; ABI-1648) has the potential for the treatment of Chlamydia infection, Clostridium difficile associated diarrhea (CDAD), and tuberculosis (TB) .
    Rifalazil
  • HY-E70236
    CoA-S-S-CoA

    		Endogenous Metabolite Others
    CoA–S-S–CoA is an endogenous metabolite found inP. furiousus. CoA–S-S–CoA is a substrate of NOXA2 .
    CoA-S-S-CoA
  • HY-141554A
    (2S,3S,11bR)-Dihydrotetrabenazine

    (2S,3S,11bR)-DHTBZ

    		 Monoamine Transporter Neurological Disease
    (2S,3S,11bR)-Dihydrotetrabenazine ((2S,3S,11bR)-DHTBZ) is a highly selective inhibitor of vesicular monoamine transporter 2 (VMAT2) with a Ki value of 593 nM. (2S,3S,11bR)-Dihydrotetrabenazine inhibits vesicular transport of monoamine neurotransmitters like dopamine and serotonin, reducing their synaptic release. (2S,3S,11bR)-Dihydrotetrabenazine is promising for research of Huntington's chorea and other hyperkinetic disorders .
    (2S,3S,11bR)-Dihydrotetrabenazine
  • HY-101955
    (2S,6S)-Hydroxynorketamine hydrochloride

    (2S,6S)-HNK hydrochloride

    		 mTOR nAChR Neurological Disease
    (2S,6S)-Hydroxynorketamine hydrochloride is a neurorelaxant with potential antidepressant and analgesic effects. (2S,6S)-Hydroxynorketamine hydrochloride can activate the mTOR pathway, increase the phosphorylation level of downstream targets, and antagonize α7-nicotinic acetylcholine receptor (nAChR) to exert neuroactive properties .
    (2S,6S)-Hydroxynorketamine hydrochloride
  • HY-137428
    (S,S)-EDDS

    		Biochemical Assay Reagents Others
    (S,S)-EDDS is a stereoisomer of EDTA (HY-Y0682), and exhibits ability to chelate metal ions. (S,S)-EDDS exhibits good biodegradability in the environment, and can be used in environmental management and biotechnology .
    (S,S)-EDDS
  • HY-50856A
    Ruxolitinib (S enantiomer)
    4 Publications Verification

    S-Ruxolitinib; S-INCB18424

    		 JAK Cancer
    Ruxolitinib (S enantiomer) (S-Ruxolitinib) is the S-enantiomer of Ruxolitinib (HY-50856). Ruxolitinib (S enantiomer) is an orally active, potent JAK inhibitor .
    Ruxolitinib (S enantiomer)
  • HY-CE00213
    (2S,5S)-5-Carboxymethylproline-CoA

    (2S,5S)-5-Carboxymethylproline-coenzyme A

    		 Biochemical Assay Reagents Others
    (2S,5S)-5-Carboxymethylproline-CoA ((2S,5S)-5-Carboxymethylproline-coenzyme A) is a derivative of Coenzyme A (HY-128851).
    (2S,5S)-5-Carboxymethylproline-CoA
  • HY-W074930
    (S)-Tenofovir

    (S)-GS 1278; (S)-PMPA; (S)-TDF

    		 HIV HBV Infection
    (S)-Tenofovir ((S)-GS 1278) is the less active S-enantiomer of Tenofovir. Tenofovir is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B (HBV) .
    (S)-Tenofovir
  • HY-14658A
    (S)-Thalidomide

    (S)-(-)-Thalidomide

    		 Molecular Glues Ligands for E3 Ligase Autophagy Apoptosis Metabolic Disease Inflammation/Immunology
    (S)-Thalidomide ((S)-(-)-Thalidomide) is the S-enantiomer of Thalidomide. (S)-Thalidomide has immunomodulatory, anti-inflammatory, antiangiogenic and pro-apoptotic effects . (S)-Thalidomide induces teratogenic effects by binding to cereblon (CRBN) .
    (S)-Thalidomide
  • HY-107661A
    S-(+)-Arundic Acid

    (S)ONO-2506; (S)-2-Propyloctanoic acid

    		 Drug Isomer Others
    S-(+)-Arundic Acid ((S)ONO-2506) is the S-enantiomer of Arundic Acid. Arundic acid is an astrocyte-modulating agent, has the potential for stroke and Alzheimer’s disease research .
    S-(+)-Arundic Acid
  • HY-141848A
    (S,S)-BMS-984923

    		mGluR Neurological Disease
    (S,S)-BMS-984923 is a less active (S,S)-enantiomer of BMS-984923. (S,S)-BMS-984923 shows an EC50 >1μM for mGluR5 receptor . BMS-984923 is a potent mGluR5 silent allosteric modulator . (S,S)-BMS-984923 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    (S,S)-BMS-984923
  • HY-14855A
    (S)-Tedizolid
    2 Publications Verification

    (S)-TR 700; (S)-DA 7157

    		 Bacterial Antibiotic Infection
    (S)-Tedizolid is the S-enantiomer of Tedizolid. Tedizolid is a novel oxazolidinone with activity against Gram-positive pathogens. (S)-Tedizolid is the less active isomer.
    (S)-Tedizolid

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