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type-II

" in MedChemExpress (MCE) Product Catalog:

123

Inhibitors & Agonists

2

Screening Libraries

10

Biochemical Assay Reagents

13

Peptides

3

Inhibitory Antibodies

7

Natural
Products

44

Recombinant Proteins

2

Isotope-Labeled Compounds

21

Antibodies

Targets Recommended:
Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-E70005B

    MMP Others
    Collagenase, Type II is a microbially derived matrix metalloproteinases (MMPs) and zinc peptidase. Collagenase, Type II breaksdown collagens1, 3, 5, 7, 8, 10, fibronectin, gelatin, aggrecann .

    Collagenase, <em>Type II</em>
  • HY-150044

    DNA/RNA Synthesis Topoisomerase Bacterial Infection
    Type II topoisomerase inhibitor 1 is a potent and selective E. coli DNA gyrase inhibitor (IC50: 1.7 nM), and forms hydrogen bonds with Asp73 residue. Type II topoisomerase inhibitor 1 inhibits topoisomerase IV activity (IC50: 0.98 μM). Type II topoisomerase inhibitor 1 can be used in the research of antibacterial area .
    <em>Type II</em> topoisomerase inhibitor 1
  • HY-163004

    Trk Receptor Cancer
    Type II TRK inhibitor 2 (compound 40l) is a selective type II TRK inhibitor with plasma stability and moderate hepatic microsomal stability. Type II TRK inhibitor 2 significantly inhibits Km-12, Ba/F3-TRKA G595R and Ba/F3-TRKA G667C cell proliferation (IC50: 4.1 nM, 41.5 nM, 1.4 nM). Type II TRK inhibitor 2 can be used to study NTRK fusion cancers .
    <em>Type II</em> TRK inhibitor 2
  • HY-146807

    Trk Receptor Cancer
    Type II TRK inhibitor 1 is a potent TRK inhibitor, which inhibits various TRK fusion protein variants and wild type. Type II TRK inhibitor 1 exhibits antiproliferative activity against Ba/F3 cells harboring CD74-TRKA G667C and ETV6-TRKC G696C fusion proteins with IC50s of 6 nM and 1.7 nM, respectively . Type II TRK inhibitor 1 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    <em>Type II</em> TRK inhibitor 1
  • HY-154972

    Glucosidase Amylases Metabolic Disease
    α-Amylase/α-Glucosidase-IN-3 (Compound 17) is an α-Amylase/α-Glucosidase dual inhibitor, with IC50s of 0.70 μM and 1.10 μM. α-Amylase/α-Glucosidase-IN-3 can be used for research of type-II diabetes mellitus .
    α-Amylase/α-Glucosidase-IN-3
  • HY-P5003

    Biochemical Assay Reagents Inflammation/Immunology
    Collagen Type II Fragment is an anti-inflammatory peptide that potently inhibits collagen-induced arthritis (CIA) in mice. Collagen Type II Fragment can be used for research on inflammation and immunity .
    Collagen <em>Type II</em> Fragment
  • HY-P9910

    GA101; Anti-Human CD20 type II, Humanized Antibody

    CD20 Cancer
    Obinutuzumab (GA101) a novel glycoengineered Type II CD20 humanized IgG1 monoclonal antibody in development for non-Hodgkin lymphoma.
    Obinutuzumab
  • HY-10326
    GW788388
    10+ Cited Publications

    TGF-β Receptor Cancer
    GW788388 is a potent and selective inhibitor of ALK5 with IC50 of 18 nM, and also inhibits TGF-β type II receptor and activin type II receptor activities, without inhibiting BMP type II receptor.
    GW788388
  • HY-A0104J

    Hypromellose (type II,Viscosity:5mPa.s); (Hydroxypropyl)methyl cellulose (type II,Viscosity:5mPa.s); Celacol HPM 5000 (type II,Viscosity:5mPa.s)

    Biochemical Assay Reagents Others
    HPMC (Hypromellose) (Type II,Viscosity:5mPa.s) is a hydrophilic, non-ionic cellulose ether used to form swellable-soluble matrices. HPMC (Type II,Viscosity:5mPa.s) is widely used in agent formulations due to its biocompatibility, uncharged nature, solubility in water and thermoplastic behavior .
    HPMC (<em>Type II</em>,Viscosity:5mPa.s)
  • HY-A0104I

    Hypromellose (type II,Viscosity:100000mPa.s); (Hydroxypropyl)methyl cellulose (type II,Viscosity:100000mPa.s); Celacol HPM 5000 (type II,Viscosity:100000mPa.s)

    Biochemical Assay Reagents Others
    Hydroxypropylmethylcellulose (Type II,Viscosity:100000mPa.s) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    HPMC (<em>Type II</em>,Viscosity:100000mPa.s)
  • HY-A0104E

    Hypromellose (type II,Viscosity:100mPa.s); (Hydroxypropyl)methyl cellulose (type II,Viscosity:100mPa.s); Celacol HPM 5000 (type II,Viscosity:100mPa.s)

    Biochemical Assay Reagents Others
    Hypromellose (Type II,Viscosity:100mPa.s) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    HPMC (<em>Type II</em>,Viscosity:100mPa.s)
  • HY-A0104H

    Hypromellose (type II,Viscosity:15000mPa.s); (Hydroxypropyl)methyl cellulose (type II,Viscosity:15000mPa.s); Celacol HPM 5000 (type II,Viscosity:15000mPa.s)

    Biochemical Assay Reagents Others
    Hypromellose (Type II,Viscosity:15000mPa.s) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    HPMC (<em>Type II</em>,Viscosity:15000mPa.s)
  • HY-A0104F

    Hypromellose (type II,Viscosity:400mPa.s); (Hydroxypropyl)methyl cellulose (type II,Viscosity:400mPa.s); Celacol HPM 5000 (type II,Viscosity:400mPa.s)

    Biochemical Assay Reagents Others
    Hypromellose (Type II,Viscosity:400mPa.s) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    HPMC (<em>Type II</em>,Viscosity:400mPa.s)
  • HY-A0104G

    Hypromellose (type II,Viscosity:4000mPa.s); (Hydroxypropyl)methyl cellulose (type II,Viscosity:4000mPa.s); Celacol HPM 5000 (type II,Viscosity:4000mPa.s)

    Biochemical Assay Reagents Others
    Hypromellose (Type II,Viscosity:4000mPa.s) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    HPMC (<em>Type II</em>,Viscosity:4000mPa.s)
  • HY-P0220

    PACAP Receptor Neurological Disease
    PACAP (6-38), human, ovine, rat is a potent PACAP receptor antagonist with IC50s of 30, 600, and 40 nM for PACAP type I receptor, PACAP type II receptor VIP1, and PACAP type II receptor VIP2, respectively.
    PACAP (6-38), human, ovine, rat
  • HY-16742
    Gepotidacin
    5+ Cited Publications

    GSK2140944

    Bacterial Topoisomerase Infection
    Gepotidacin (GSK2140944) is a novel triazaacenaphthylene bacterial type II topoisomerase inhibitor.
    Gepotidacin
  • HY-110304

    mGluR Neurological Disease
    NPEC-caged-LY379268 is a type II mGluR agonist .
    NPEC-caged-LY379268
  • HY-P0220A
    PACAP (6-38), human, ovine, rat TFA
    1 Publications Verification

    PACAP Receptor Neurological Disease
    PACAP (6-38), human, ovine, rat TFA is a potent PACAP receptor antagonist with IC50s of 30, 600, and 40 nM for PACAP type I receptor, PACAP type II receptor VIP1, and PACAP type II receptor VIP2, respectively.
    PACAP (6-38), human, ovine, rat TFA
  • HY-114632

    Others Metabolic Disease
    Oxeglitazar is an orally active compound that can be used for the research of type II diabetes .
    Oxeglitazar
  • HY-P0221
    PACAP (1-38), human, ovine, rat
    3 Publications Verification

    Pituitary Adenylate Cyclase Activating Polypeptide 38

    PACAP Receptor Neurological Disease
    PACAP (1-38), human, ovine, rat is a neuropeptide with 38 amino acid residues. PACAP (1-38) binds to PACAP type I receptor, PACAP type II receptor VIP1, and PACAP type II receptor VIP2 with IC50s of 4 nM, 2 nM, and 1 nM, respectively.
    PACAP (1-38), human, ovine, rat
  • HY-100600

    K03859

    BGG463 (K03859) is an orally active type II CDK2 inhibitor .
    BGG463
  • HY-P0221A

    Pituitary Adenylate Cyclase Activating Polypeptide 38 TFA

    PACAP Receptor Neurological Disease
    PACAP (1-38), human, ovine, rat TFA is a neuropeptide with 38 amino acid residues. PACAP (1-38) binds to PACAP type I receptor, PACAP type II receptor VIP1, and PACAP type II receptor VIP2 with IC50s of 4 nM, 2 nM, and 1 nM, respectively.
    PACAP (1-38), human, ovine, rat TFA
  • HY-76938

    4-Acetylaminophenylacetic acid; MS-932

    Others Inflammation/Immunology
    Actarit, an orally active antirheumatic compound, has the potential to treat type II collagen-induced arthritis .
    Actarit
  • HY-15465
    KN-93
    Maximum Cited Publications
    54 Publications Verification

    CaMK Autophagy Cancer
    KN-93 is a cell-permeable, reversible and competitive inhibitor calmodulin-dependent kinase type II (CaMKII) with a Ki of 370 nM.
    KN-93
  • HY-15465A
    KN-93 hydrochloride
    Maximum Cited Publications
    54 Publications Verification

    CaMK Autophagy Cancer
    KN-93 hydrochloride is a cell-permeable, reversible and competitive inhibitor calmodulin-dependent kinase type II (CaMKII) with a Ki of 370 nM.
    KN-93 hydrochloride
  • HY-101267
    CHMFL-BMX-078
    1 Publications Verification

    CHMFL-BMX 078

    BMX Kinase Cancer
    CHMFL-BMX-078 is a highly potent and selective type II irreversible BMX kinase inhibitor with an IC50 of 11 nM.
    CHMFL-BMX-078
  • HY-13635
    Finasteride
    4 Publications Verification

    MK-906

    5 alpha Reductase Cancer
    Finasteride (MK-906) is a potent and competitive 5α-reductase inhibitor, with an IC50 of 4.2 nM for type II 5α-reductase. Finasteride has approximately a 100-fold greater affinity for type II 5α-reductase enzyme than for the type I enzyme. Finasteride can be used for the research of benign prostatic hyperplasia (BPH) and androgenic alopecia .
    Finasteride
  • HY-13635A

    MK-906 acetate

    5 alpha Reductase Cancer
    Finasteride (MK-906) acetate is a potent and competitive 5α-reductase inhibitor, with an IC50 of 4.2 nM for type II 5α-reductase. Finasteride acetate has approximately a 100-fold greater affinity for type II 5α-reductase enzyme than for the type I enzyme. Finasteride acetate can be used for the research of benign prostatic hyperplasia (BPH) and androgenic alopecia .
    Finasteride acetate
  • HY-19900
    ITX5061
    2 Publications Verification

    p38 MAPK Autophagy HCV Infection
    ITX5061 is a type II inhibitor of p38 MAPK and also an antagonist of scavenger receptor B1 (SR-B1).
    ITX5061
  • HY-145985

    Bacterial Infection
    CBR-3465 is a mycobacterium tuberculosis (Mtb) type II NADH dehydrogenase inhibitor, with the MIC of 0.16 μM against Mtb .
    CBR-3465
  • HY-145986

    Bacterial Infection
    CBR-6672 is a mycobacterium tuberculosis (Mtb) type II NADH dehydrogenase inhibitor, with the MIC of 0.14 μM against Mtb .
    CBR-6672
  • HY-18960
    CHZ868
    5 Publications Verification

    JAK Cancer
    CHZ868 is a type II JAK2 inhibitor with an IC50 of 0.17 μM in EPOR JAK2 WT Ba/F3 cell.
    CHZ868
  • HY-N3269

    Others Others
    Methyl p-hydroxyphenyllactate (MeHPLA) is an important cell growth-regulating agent which binds to nuclear type II binding sites in normal and malignant cells .
    Methyl p-hydroxyphenyllactate
  • HY-147729

    DNA/RNA Synthesis Infection
    UIAA-II-232 (compound 19b) is a potent DNA gyrase catalytic inhibitor with an IC50 value of 3.5 µM .
    UIAA-II-232
  • HY-125857

    Biochemical Assay Reagents Apoptosis Reactive Oxygen Species Metabolic Disease
    Cytochrome C is a multi-functional enzyme involving in life and death decisions of the cell. Cytochrome C is essential in mitochondrial electron transport and intrinsic type II apoptosis .
    Cytochrome C
  • HY-13635S

    MK-906-d9

    Isotope-Labeled Compounds 5 alpha Reductase Cancer
    Finasteride-d9 is deuterium labeled Finasteride. Finasteride (MK-906) is a potent and competitive 5α-reductase inhibitor, with an IC50 of 4.2 nM for type II 5α-reductase. Finasteride has approximately a 100-fold greater affinity for type II 5α-reductase enzyme than for the type I enzyme. Finasteride can be used for the research of benign prostatic hyperplasia (BPH) and androgenic alopecia[1][2][3].
    Finasteride-d9
  • HY-13635R

    MK-906 (Standard)

    5 alpha Reductase Cancer
    Finasteride (Standard) is the analytical standard of Finasteride. This product is intended for research and analytical applications. Finasteride (MK-906) is a potent and competitive 5α-reductase inhibitor, with an IC50 of 4.2 nM for type II 5α-reductase. Finasteride has approximately a 100-fold greater affinity for type II 5α-reductase enzyme than for the type I enzyme. Finasteride can be used for the research of benign prostatic hyperplasia (BPH) and androgenic alopecia .
    Finasteride (Standard)
  • HY-16619

    Free Fatty Acid Receptor Metabolic Disease
    AM-5262 is a GPR40 full agonist with an EC50 value of 0.081 μM. AM-5262 can be used for the research of type II diabetes .
    AM-5262
  • HY-161057

    Bcr-Abl Inflammation/Immunology Cancer
    HG-7-86-01 (Compound 26) is type II tyrosine kinase inhibitor. HG-7-86-01 has anti-proliferative activity .
    HG-7-86-01
  • HY-15004
    AUZ 454
    4 Publications Verification

    K03861

    CDK Cancer
    AUZ 454 (K03861) is a type II CDK2 inhibitor with Kd of 8.2 nM. AUZ 454 (K03861) inhibits CDK2 activity by competing with binding of activating cyclins.
    AUZ 454
  • HY-12149

    nAChR Neurological Disease
    A-867744 is a highly potent and selective type II positive allosteric modulator (PAM) of the alpha7 nicotinic acetylcholine receptors (nAChR) with an EC50 of 1.0 μM .
    A-867744
  • HY-112089
    Naporafenib
    2 Publications Verification

    LXH254

    Raf p38 MAPK Bcr-Abl Cancer
    Naporafenib (LXH254) is a potent, selective, orally active, type II BRAF and CRAF inhibitor, with IC50 values of 0.072 and 0.21 nM against CRAF and BRAF, respectively .
    Naporafenib
  • HY-111507

    PDGFR Cancer
    PDGFRα kinase inhibitor 1 is a highly selective type II PDGFRα kinase inhibitor with IC50s of 132 nM and 6115 nM for PDGFRα and PDGFRβ, respectively .
    PDGFRα kinase inhibitor 1
  • HY-145872

    HBV Infection
    HBV-IN-20 is a potent and oral active HBV inhibitor with an EC50 of 0.46 µM. HBV-IN-20 is a typical type II CpAM (core protein assembly modulators) .
    HBV-IN-20
  • HY-100875
    Bisantrene
    5 Publications Verification

    CL216942

    Topoisomerase Cancer
    Bisantrene is a highly effective antitumor agent, it exerts its cytotoxicity by affecting DNA intercalation. Bisantrene targets eukaryotic type II topoisomerases. Bisantrene is a substrate of MDR1 .
    Bisantrene
  • HY-100875A
    Bisantrene dihydrochloride
    5 Publications Verification

    CL-216942 dihydrochloride

    Topoisomerase Cancer
    Bisantrene dihydrochloride is a highly effective antitumor agent, it exerts its cytotoxicity by affecting DNA intercalation. Bisantrene dihydrochloride targets eukaryotic type II topoisomerases. Bisantrene dihydrochloride is a substrate of MDR1 .
    Bisantrene dihydrochloride
  • HY-135130

    (-)-BABX

    Bacterial Infection
    Bischloroanthrabenzoxocinone is a potent Type II fatty acid synthesis (FASII) inhibitor. Bischloroanthrabenzoxocinone inhibits fatty acid synthesis. Bischloroanthrabenzoxocinone shows antibacterial activities and inhibits phospholipid, DNA, RNA, protein, and cell wall synthesis .
    Bischloroanthrabenzoxocinone
  • HY-110178

    MAGL Inflammation/Immunology
    WWL123, a carbamate-based compound, is a potent and selective ABHD6 inhibitor. WWL123 can be used for research of inflammation, metabolic disorders (obesity and type II diabetes mellitus) and epilepsy .
    WWL123
  • HY-N12191

    HSV Others
    Cangorinine E-1 (compound 11) is a dihydroagarofuran derivative of the sesquiterpenoid family. Cangorinine E-1 exhibits weak inhibitory effects on herpes simplex virus type II (HSV) .
    Cangorinine E-1
  • HY-162042

    AMPK Metabolic Disease
    AMPK activator 14 (compound 32) is an orally active AMPK activator. AMPK activator 14 decreases fasted glucose and insulin levels in a db/db mouse model of Type II diabetes .
    AMPK activator 14

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