38 Results for "

SANK 60501

" in MedChemExpress (MCE) Product Catalog:
Products (38)

38 Results for "SANK 60501" in MCE Product Catalog:

67
67 Publications Verification
Cat. No.: HY-15768
CAS No.: 142880-36-2
Purity:  98.39%
Synonyms: GM6001; Galardin
Target:  

MMP

Research Areas:  

Cancer

Ilomastat (GM6001) is a potent and broad spectrum matrix metalloprotease (MMP) inhibitor, inhibits MMPs (IC50s, 1.5 nM for MMP-1; 1.1 nM for MMP-2; 1.9 nM for MMP-3; 0.5 nM for MMP-9), with a Ki of 0.4 nM for human skin fibroblast collagenase (MMP-1).
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3
3 Cited Publications
Cat. No.: HY-131003
CAS No.: 1505515-69-4
Purity:  99.78%
Synonyms: DS-6051b; AB-106; IBI-344
Target:  

ROS Kinase

Research Areas:  

Cancer

Taletrectinib (DS-6051b) is a potent, orally active, and next-generation selective ROS1/NTRK inhibitor. Taletrectinib potently inhibits recombinant ROS1, NTRK1, NTRK2, and NTRK3 with IC50s of 0.207, 0.622, 2.28, and 0.98 nM, respectively. Taletrectinib also inhibits ROS1 G2032R and other Crizotinib-resistant ROS1 mutants .
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1
1 Cited Publications
Cat. No.: HY-106048
CAS No.: 56973-26-3
Purity:  99.82%
Synonyms: 5-Hydroxy-1H-imidazole-4-carboxamide; FF-10501
Research Areas:  

Others

Bredinin aglycone (5-Hydroxy-1H-imidazole-4-carboxamide) is a purine nucleotide analogue. Bredinin aglycone can be used to examine the efficiency of catalysts for the preparation of purine nucleotide analogues .
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Cat. No.: HY-P99191
CAS No.: 1709815-23-5
Synonyms: NI-0501

Target:  

IFNAR

Research Areas:  

Inflammation/Immunology

Emapalumab (NI-0501) is a human monoclonal IgG1 antibody that noncompetitively inhibits IFN-γ. Emapalumab binds with high affinity (Kd= 1.4 pM) to both free IFN-γ as well as IFN-γ bound to its receptor. Emapalumab can be used in research of hemophagocytic lymphohistiocytosis (HLH) .
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Cat. No.: HY-19929
CAS No.: 1239278-59-1
Synonyms: CHF-6001
Tanimilast (CHF-6001) is an orally active and selective phosphodiesterase 4 inhibitor (IC50=0.026 nM) with robust anti-inflammatory activity and suitable for topical pulmonary administration. Tanimilast increases cellular cAMP levels, and inhibits NF-κB signaling pathway. Tanimilast is used for the research of obstructive lung diseases .
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Cat. No.: HY-P990040
CAS No.: 2642171-64-8
Synonyms: LVGN-6051

Target:  

TNF Receptor

Research Areas:  

Cancer

Exlinkibart (LVGN-6051) targets TNFRSF9 and is an IgG1κ antibody humanized through complementarity-determining region (CDR) grafting technology.
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Cat. No.: HY-P9994
CAS No.: 2500674-05-3
Synonyms: SBT6050
Pertuzumab zuvotolimod (SBT6050) is an anti-HER2 antibody-drug conjugate (ADC). Pertuzumab zuvotolimod is composed of a humanized anti-HER2 antibody (Pertuzumab) (HY-P9912A), a linker, a TLR8 agonist payload, and the drug-linker conjugate for ADC is Zuvotolimod (HY-145620). Pertuzumab zuvotolimod potently induces multiple anti-tumor immune activities through the direct activation myeloid cells and the subsequent induction of T and NK cell cytolytic activity. Pertuzumab zuvotolimod can be used for HER2-expressing solid tumors research .
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Cat. No.: HY-106959
CAS No.: 82664-20-8
Purity:  99.73%
Synonyms: (8S)-8-Fluoroerythromycin A; P-0501A
Target:  

Antibiotic Bacterial

Research Areas:  

Infection

Flurithromycin ((8S)-8-Fluoroerythromycin A) is an orally active broad spectrum antibiotic. Flurithromycin can be used in the research of bacterial infections .
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Cat. No.: HY-131003A
CAS No.: 1505514-27-1
Synonyms: DS-6051b free base; AB-106 free base; IBI-344 free base
Target:  

ROS Kinase

Research Areas:  

Cancer

Taletrectinib (DS-6051b) free base is a potent, orally active, and next-generation selective ROS1/NTRK inhibitor. Taletrectinib free base potently inhibits recombinant ROS1, NTRK1, NTRK2, and NTRK3 with IC50s of 0.207, 0.622, 2.28, and 0.98 nM, respectively. Taletrectinib free base also inhibits ROS1 G2032R and other Crizotinib-resistant ROS1 mutants .
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Cat. No.: HY-P991566
CAS No.: 2983061-18-1

Target:  

CTLA-4

Research Areas:  

Cancer

KD6001 is a humanized IgG1κ monoclonal antibody, targeting CTLA4. KD6001 significantly disrupts CTLA-4 interactions with CD80 (IC50: 16 ng/mL) and CD86. KD6001 enhances IL-2 and IFNγ expression in PHA-activated human lymphocytes and exhibits potent antitumor effects. KD6001 effectively inhibits tumor growth in MC38, B16, and Hepa1-6 tumor mice model. KD6001 can be used for cancers research, such as advanced melanoma, hepatocellular carcinoma and liver cancer .
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Cat. No.: HY-15768R
CAS No.: 142880-36-2
Synonyms: GM6001 (Standard); Galardin (Standard)
Target:  

MMP Reference Standards

Research Areas:  

Cancer

Ilomastat (Standard) is the analytical standard of Ilomastat. This product is intended for research and analytical applications. Ilomastat (GM6001) is a potent and broad spectrum matrix metalloprotease (MMP) inhibitor, inhibits MMPs (IC50s, 1.5 nM for MMP-1; 1.1 nM for MMP-2; 1.9 nM for MMP-3; 0.5 nM for MMP-9), with a Ki of 0.4 nM for human skin fibroblast collagenase (MMP-1).
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Cat. No.: HY-106138
CAS No.: 140703-49-7
Synonyms: Meterelin; MF 6001
Target:  

GnRH Receptor

Research Areas:  

Cancer

Avorelin (Meterelin) is a gonadotropin releasing hormone (GnRH) agonist. Avorelin can be used of the study of prostate cancer .
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Cat. No.: HY-101643
CAS No.: 117705-18-7
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

RP-60503 is an orally active anxiolytic cyclopyrrolone derivative with low sedative potential. RP-60503 binds to the gamma-aminobutyric acidA (GABA)/benzodiazepine receptor with a Ki value of 1.16 nM. RP-60503 can be used for the research of neurological disease .
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Cat. No.: HY-19929A
Synonyms: (R)-CHF-6001
Research Areas:  

Inflammation/Immunology

(R)-Tanimilast is a isomeride of Tanimilast (HY-19929). Tanimilast (CHF-6001) is a novel highly potent and selective phosphodiesterase 4 inhibitor (IC50=0.026 nM) .
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Cat. No.: HY-R01929
Target:  

MicroRNA

Research Areas:  

Cancer

hsa-miR-6501-3p mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.
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Cat. No.: HY-R01930
Target:  

MicroRNA

Research Areas:  

Cancer

hsa-miR-6501-5p mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.
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Cat. No.: HY-RI01930
Target:  

MicroRNA

Research Areas:  

Cancer

hsa-miR-6501-5p inhibitors are chemically-modified oligonucleotides that hybridize with mature miRNAs. The miRNA inhibitors have full-length nucleotide 2'-methoxy modification. The miRNA inhibitors strongly compete with mature miRNAs to prevent the complementary pairing of miRNAs and their target genes, thereby inhibiting miRNAs from functioning.
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Cat. No.: HY-106048R
CAS No.: 56973-26-3
Synonyms: 5-Hydroxy-1H-imidazole-4-carboxamide (Standard); FF-10501 (Standard)
Bredinin aglycone (Standard) is the analytical standard of Bredinin aglycone. This product is intended for research and analytical applications. Bredinin aglycone (5-Hydroxy-1H-imidazole-4-carboxamide) is a purine nucleotide analogue. Bredinin aglycone can be used to examine the efficiency of catalysts for the preparation of purine nucleotide analogues[1].
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Cat. No.: HY-W182790
CAS No.: 150985-54-9
Synonyms: LSL 60101
Garsevil (LSL 60101) is a biphasic, selective imidazoline I2 receptor (I2-IR) ligand, with a pKi of 9.03 and a Ki of 0.9 nM at the high-affinity site, and a pKi of 5.25 and a Ki of 5.6 nM at the low-affinity site. Garsevil is applicable to research related to Alzheimer's disease .
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Cat. No.: HY-189002
CAS No.: 866554-59-8
Synonyms: ZHD 0501
Target:  

Others

Research Areas:  

Cancer

ACT-007 (ZHD 0501) is an indolocarbazole alkaloid derived from Actinomadura sp., which selectively inhibits the proliferation of lung cancer cells and induces G2/M phase cell cycle arrest in breast cancer cells. ACT-007 can be applied in the research of lung cancer and breast cancer .
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