70 Results for "

S7

" in MedChemExpress (MCE) Product Catalog:
Products (70)

70 Results for "S7" in MCE Product Catalog:

1
1 Cited Publications
Art. -Nr.: HY-P10284
CAS. Nr.: 853248-13-2
Forschungsgebiete:  

Cardiovascular Disease Cancer

S7 is an inhibitory polypeptide targeting IL-6R, which specifically binds to IL-6R and its A chain (gp80/IL-6RA) to block its signal transduction. S7 inhibits IL-6-mediated anti-apoptosis (apoptosis), angiogenesis and the expression of VEGF-A, blocks related survival signaling pathways, and enhances the sensitivity of cancer cells to chemotherapeutic drugs. S7 can be applied to the research of related diseases such as cervical cancer, multiple myeloma, Kaposi's sarcoma, prostate cancer and basal cell carcinoma .
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34
34 Publications Verification
Art. -Nr.: HY-14622A
CAS. Nr.: 852391-15-2
Reinheit:  99.65%
Synonyms: Necrostatin 1S; Nec-1S; 7-Cl-O-Nec1
Target:  

RIP kinase

Forschungsgebiete:  

Cancer

Necrostatin 2 racemate (Nec-1S), the Necrostatin-1 (HY-15760) stable, is a potent and specific RIPK1 inhibitor lacking the IDO-targeting effect .
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4
4 Cited Publications
Art. -Nr.: HY-P80616
Synonyms: FOS; G0S7; Proto-oncogene c-Fos; Cellular oncogene fos; G0/G1 switch regulatory protein 7

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, ELISA

Reactivity:  

Human, Mouse, Rat

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2
2 Cited Publications
Art. -Nr.: HY-P80081
Synonyms: G0S7, FOS, Protein c-Fos, Cellular oncogene fos, G0/G1 switch regulatory protein 7, Proto-oncogene c-Fos, Transcription factor AP-1 subunit c-Fos

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF

Reactivity:  

Human, Rat

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1
1 Cited Publications
Art. -Nr.: HY-100559
CAS. Nr.: 853625-60-2
Reinheit:  99.70%
Target:  

Apoptosis

Forschungsgebiete:  

Metabolic Disease Endocrinology Cancer

SecinH3 is an antagonist of cytohesins with IC50s of 5.4 μM, 2.4 μM, 5.4 μM, 5.6 μM, 5.6 μM and 65 μM for hCyh1, hCyh2, mCyh3, hCyh3, drosophila steppke and yGea2-S7, respectively.
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Art. -Nr.: HY-159520
CAS. Nr.: 2731294-23-6
Synonyms: Ofirnoflast; HT-6184
Ofirnoflastum (Ofirnoflast) is an orally active first-in-class allosteric NEK7 inhibitor with an IC50 of 46 nM. Ofirnoflastum binds an allosteric site adjacent to NEK7’s ATP-binding pocket, induces conformational shifts, disrupts NEK7-NLRP3 binding, blocks NLRP3 inflammasome assembly, spares NEK7’s physiological functions, and suppresses caspase-1, caspase-8, NF-κB, and TNF activity. Ofirnoflastum reduces pro-inflammatory cytokine production, suppresses ASC specks, IL-1β release, pyroptotic cell death, and leukemic burden, induces apoptosis and erythroid differentiation, restores hematopoiesis, and improves outcomes in colitis models. Ofirnoflastum can be used for the research of myelodysplastic syndromes, chronic myelomonocytic leukemia, and acute myeloid leukemia .
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Art. -Nr.: HY-W106164A
CAS. Nr.: 2820537-15-1
Target:  

Drug Intermediate

Forschungsgebiete:  

Others

((2S,7aS)-2-Fluorohexahydro-1H-pyrrolizin-7a-yl)methanol is a drug intermediate for synthesis of various active compounds.
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Art. -Nr.: HY-133885
CAS. Nr.: 856925-75-2
S-(-)-7-Desmethyl-8-nitro blebbistatin (compound 12) is an analog of (-)-Blebbistatin (HY-13441). (-)-Blebbistatin is a selective non-muscle myosin II inhibitor .
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Art. -Nr.: HY-N2207
CAS. Nr.: 178740-32-4
rel-(8R,8'R)-Dimethyl-(7S,7'R)-bis(3,4-methylenedioxyphenyl)tetrahydro-furan is a chemical constituent of the fruit of Myristica fragrans.
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Art. -Nr.: HY-W091788
CAS. Nr.: 908130-61-0
Forschungsgebiete:  

Others

(2S,3R,5S)-7-Deaza-2'-deoxy-7-iodoadenosine is the isomer of 7-Deaza-2'-deoxy-7-iodoadenosine (HY-W048490), and can be used as an experimental control. 7-Deaza-2'-deoxy-7-iodoadenosine is a modified oligonucleotide containing 7-Deazaadenine .
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Art. -Nr.: HY-174129
CAS. Nr.: 2649008-95-5
Target:  

Btk Apoptosis

Forschungsgebiete:  

Cancer

TM471-1 is an orally active and covalent Bruton's tyrosine kinase (BTK) inhibitor with IC50 values of 1.3 nM (BTK WT), >40,000 nM (BTK C481S), 7.9 nM (TEC) and 12.4 nM (TXK). TM471-1 inhibits cell growth in vivo and in vitro, arrests cell cycle at G0/G1 phase and induces cell apoptosis .
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Art. -Nr.: HY-163892
Target:  

DNA/RNA Synthesis

Forschungsgebiete:  

Cancer

POLRMT-IN-1 (compound S7) is a POLRMT inhibitor. POLRMT-IN-1 can be used in cancer-related research .
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Art. -Nr.: HY-162578
Target:  

PPAR

Forschungsgebiete:  

Metabolic Disease

PPARα/γ agonist 4 (Compound (S)-7) is an orally active dual potent agonist of PPARα and PPARγ, with EC50 values of 0.061 μM and 1.42 μM respectively. PPARα/γ agonist 4 acts through an insulin-independent mechanism and exhibits mitochondrial pyruvate carrier inhibition and anti-diabetic properties. PPARα/γ agonist 4 is expected to be used in research for dyslipidemic type 2 diabetes .
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Art. -Nr.: HY-N0291R
CAS. Nr.: 29745-04-8
Forschungsgebiete:  

Inflammation/Immunology Cancer

(±)-Norcantharidin (Standard) is the analytical standard of (±)-Norcantharidin. This product is intended for research and analytical applications. (±)-Norcantharidin ((±)-NCTD) is a compound possessing anti-angiogenetic activity with potential use in anti-cancertherapy. (±)-Norcantharidin could prevent tumorigenesis by inhibiting cell proliferation, inducing apoptosis and the cell cycle arrest, and anti-angiogenic effects .
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Art. -Nr.: HY-145177
CAS. Nr.: 1799711-31-1
Reinheit:  98.43%
Forschungsgebiete:  

Cancer

Thalidomide-O-amido-CH2-PEG3-CH2-NH-Boc is a synthesized E3 ligase ligand-linker conjugate. Thalidomide-O-amido-CH2-PEG3-CH2-NH-Boc incorporates the Thalidomide based cereblon ligand and a linker. Thalidomide-O-amido-CH2-PEG3-CH2-NH-Boc can be used for the synthesis of PROTAC BET degrader . (From patent WO2017180417A1 compound s7).
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Art. -Nr.: HY-W742809
CAS. Nr.: 63740-81-8
Target:  

Drug Derivative

Forschungsgebiete:  

Others

(S)-7-Hydroxywarfarin is the S stereoisomer of 7-Hydroxywarfarin (HY-139167). (S)-7-Hydroxywarfarin is the inactive, major metabolite of racemic Warfarin (HY-B0687) .
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Art. -Nr.: HY-P71266
Reinheit:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: RPS7; S7; Ribosomal Protein S7; Small Ribosomal Subunit Protein ES7; 40S Ribosomal Protein S7; DBA8; ES7
Species:  
Source:  
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Art. -Nr.: HY-N2747
CAS. Nr.: 100079-34-3
2(S)-7-Hydroxy-5,8,2'-trimethoxyflavanone is a natural flavanone compound .
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Art. -Nr.: HY-B0395DS
Synonyms: (1R,2S,7R)-DU6859a-d4 hydrochloride
(1R,2S,7R)-Sitafloxacin-d4 hydrochloride is deuterium labeled (1R,2S,7R)-Sitafloxacin hydrochloride (HY-B0395D). (R)-Sitafloxacin (DU-6857), a stereoisomer of Sitafloxacin (DU-6859a), is also an inhibitor of topoisomerases, with an IC50 of 0.18 μg/mL of DNA gyrase .
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Art. -Nr.: HY-N12068
CAS. Nr.: 214627-06-2
(S)-7-O-Methylpeucedanol 3′-O-β-D-glucopyranoside is a kind of coumarin glycoside .
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