271 Results for "

Arg6-Arg7 loop

" in MedChemExpress (MCE) Product Catalog:
Products (271)

271 Results for "Arg6-Arg7 loop" in MCE Product Catalog:

19
19 Publications Verification
Art. -Nr.: HY-17468
CAS. Nr.: 28395-03-1
Synonyms: Ro 10-6338; PF 1593
Target:  

NKCC

Forschungsgebiete:  

Cardiovascular Disease Metabolic Disease

Bumetanide (Ro 10-6338; PF 1593), a highly potent loop diuretic, is a Na +-K +-Cl + cotransporter (NKCC) blocker. Bumetanide is a selective NKCC1 inhibitor, but also inhibits NKCC2, with IC50s of 0.68 μM and 4.0 μM for hNKCC1A and hNKCC2A, respectively .
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18
18 Cited Publications
Art. -Nr.: HY-12795
CAS. Nr.: 1383716-33-3
Reinheit:  99.79%
Target:  

PI3K Autophagy

Forschungsgebiete:  

Cancer

Vps34-IN-1 is a potent and selective inhibitor of class III Vps34 PI3K. Vps34-IN-1 inhibits phosphorylation of PtdIns by recombinant insect cell expressed Vps34-Vps15 complex with an IC50 of ~25 nM. Vps34-IN-1 can suppress SGK3 activation by reducing PtdIns(3)P levels via lowering phosphorylation of T-loop and hydrophobic motifs. Vps34-IN-1 modulates autophagy .
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15
15 Cited Publications
Art. -Nr.: HY-101561
CAS. Nr.: 1703793-34-3
Reinheit:  99.75%
Synonyms: BLU-285
Target:  

c-Kit PDGFR

Forschungsgebiete:  

Cancer

Avapritinib (BLU-285) is a highly potent, selective, and orally active KIT and PDGFRA activation loop mutant kinases inhibitor with IC50s of 0.27 and 0.24 nM for KIT D816V and PDGFRA D842V, respectively. Avapritinib (BLU-285) binds the active conformation of the kinase and shows antitumor activity. Avapritinib (BLU-285) attenuates the transport function of both ABCB1 and ABCG2 .
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9
9 Cited Publications
Art. -Nr.: HY-106178
CAS. Nr.: 219639-75-5
Reinheit:  99.98%
Synonyms: 3D53
PMX-53 (3D53) is a synthetic peptidic and a potent and orally active complement C5a receptor (CD88) antagonist with an IC50 of 20 nM. PMX-53 is also a low-affinity MrgX2 agonist that stimulates MrgX2-mediated mast cell degranulation. PMX-53 specifically binds to C5aR1 and does not bind to the second C5aR (C5L2) and C3aR. PMX-53 has anti-inflammatory, anticancer and antiatherosclerotic effects .
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9
9 Cited Publications
Art. -Nr.: HY-P1082
CAS. Nr.: 197250-15-0
Forschungsgebiete:  

Cardiovascular Disease

Gap 26 is a connexin mimetic peptide, composed of residue numbers 63-75 of the first extracellular loop of connexin 43 (gap junction blocker), containing the SHVR amino acid motif .
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9
9 Cited Publications
Art. -Nr.: HY-P1082A
Forschungsgebiete:  

Cardiovascular Disease

Gap 26 TFA is a connexin mimetic peptide, composed of residue numbers 63-75 of the first extracellular loop of connexin 43 (gap junction blocker), containing the SHVR amino acid motif .
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9
9 Cited Publications
Art. -Nr.: HY-P80704
Synonyms: HIF1A; BHLHE78; MOP1; PASD8; Hypoxia-inducible factor 1-alpha; HIF-1-alpha; HIF1-alpha; ARNT-interacting protein; Basic-helix-loop-helix-PAS protein MOP1; Class E basic helix-loop-helix protein 78; bHLHe78; Member of PAS protein 1; PAS doma

Host:  

Rabbit

Application:  

WB, ICC/IF, ELISA

Reactivity:  

Human, Mouse, Rat

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7
7 Cited Publications
Art. -Nr.: HY-P0139
CAS. Nr.: 198284-64-9
Target:  

Gap Junction Protein

Forschungsgebiete:  

Cardiovascular Disease

Gap 27, a synthetic connexin43 mimetic peptide, is a gap junction inhibitor. Gap 27 possesses conserved sequence homology to a portion of the second extracellular loop leading into the fourth transmembrane connexin segment .
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7
7 Cited Publications
Art. -Nr.: HY-P80626
Synonyms: MYC; BHLHE39; Myc proto-oncogene protein; Class E basic helix-loop-helix protein 39; bHLHe39; Proto-oncogene c-Myc; Transcription factor p64

Host:  

Rabbit

Application:  

WB, ICC/IF, IP

Reactivity:  

Human, Mouse, Rat

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5
5 Cited Publications
Art. -Nr.: HY-P1136
CAS. Nr.: 1507930-57-5
Target:  

Gap Junction Protein

Forschungsgebiete:  

Cardiovascular Disease

Gap19, a peptide derived from nine amino acids of the Cx43 cytoplasmic loop (CL), is a potent and selective connexin 43 (Cx43) hemichannel blocker. Gap19 inhibits hemichannels caused by preventing intramolecular interactions of the C-terminus (CT) with the CL. Gap19 is not blocking GJ channels or Cx40/pannexin-1 hemichannels. Gap19 has protective effects against myocardial .
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5
5 Cited Publications
Art. -Nr.: HY-P1136A
Target:  

Gap Junction Protein

Forschungsgebiete:  

Cardiovascular Disease

Gap19 TFA, a peptide derived from nine amino acids of the Cx43 cytoplasmic loop (CL), is a potent and selective connexin 43 (Cx43) hemichannel blocker. Gap19 TFA inhibits hemichannels caused by preventing intramolecular interactions of the C-terminus (CT) with the CL. Gap19 TFA is not blocking GJ channels or Cx40/pannexin-1 hemichannels. Gap19 TFA has protective effects against myocardial .
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5
5 Cited Publications
Art. -Nr.: HY-15815
CAS. Nr.: 1619994-69-2
Reinheit:  99.89%
Forschungsgebiete:  

Cancer

Bromosporine, a chemical probe, is a potent BET inhibitor with an IC50 value of 2.1 μM for PCAF. Bromosporine can arrest cell cycle and induce apoptosis in cancer cells. Bromosporine exhibits excellent antitumor activity in xenograft mice model when combined with 5-Fluorouracil (HY-90006). Bromosporine can increase CDK9 T-loop phosphorylation in HIV-1 latency models, resulting the protection of reactivate HIV-1 replication from latency. Bromosporine can be used to research colorectal cancer, acute myeloid leukemia (AML) and AIDS .
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4
4 Cited Publications
Art. -Nr.: HY-124691
CAS. Nr.: 688342-78-1
Reinheit:  99.70%
Target:  

DNA/RNA Synthesis

Forschungsgebiete:  

Cancer

D-I03 is a selective RAD52 inhibitor with a Kd of 25.8 μM. D-I03 specifically inhibits RAD52-dependent single-strand annealing (SSA) and D-loop formation with IC50s of 5 μM and 8 μM, respectively. D-I03 suppresses growth of BRCA1- and BRCA2-deficient cells and inhibits formation of damage-induced RAD52 foci, but does not effect on RAD51 foci induced by Cisplatin .
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4
4 Cited Publications
Art. -Nr.: HY-P74888
Reinheit:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: HIF1A; Basic-Helix-loop-Helix-PAS Protein MOP1; Hypoxia Inducible Factor 1 Subunit Alpha; HIF-1-Alpha; BHLHe78; Hypoxia Inducible Factor 1 Alpha Subunit; PASD8; Hypoxia-Inducible Factor1alpha; MOP1; Member Of PAS Superfamily 1; Class E Basic Helix-loop-Helix Protein 78; ARNT Interacting Protein; Hypoxia-Inducible Factor 1-Alpha; ARNT-Interacting Protein; PAS Domain-Containing Protein 8; HIF1-ALPHA; Member Of PAS Protein 1; HIF1-Alpha; HIF-1alpha; BHLHE78; HIF1; HIF-1A; Hypoxia Inducible Factor 1, Alpha Subunit (Basic Helix-loop-Helix Transcription Factor)
Species:  
Human
Source:  
E. coli
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3
3 Cited Publications
Art. -Nr.: HY-107321
CAS. Nr.: 27589-33-9
Reinheit:  99.85%
Target:  

NKCC

Forschungsgebiete:  

Metabolic Disease

Azosemide, a sulfonamide loop diuretic, is a potent NKCC1 inhibitor with IC50s of 0.246 μM and 0.197 μM for hNKCC1A and NKCC1B, respectively .
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3
3 Cited Publications
Art. -Nr.: HY-W011400
CAS. Nr.: 566914-00-9
Target:  

MyD88

Forschungsgebiete:  

Inflammation/Immunology

TLR1 (compound 4a) is a low molecular weight, cell-penetrating Toll/IL-1 receptor/resistance (TIR) domain/BB-Loop mimic. TLR1 inhibits IL-1 receptor-mediated responses .
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3
3 Cited Publications
Art. -Nr.: HY-P80900
Synonyms: SREBF1; BHLHD1; SREBP1; Sterol regulatory element-binding protein 1; SREBP-1; Class D basic helix-loop-helix protein 1; bHLHd1; Sterol regulatory element-binding transcription factor 1

Host:  

Rabbit

Application:  

WB, ELISA

Reactivity:  

Human, Mouse, Rat

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3
3 Cited Publications
Art. -Nr.: HY-W012078
CAS. Nr.: 838-07-3
Synonyms: 5-Methyldeoxycytidine
5-Methyl-2'-deoxycytidine (5mdC) is an endogenous substrate of DNA methyltransferases (such as mammalian 5-C-MTase) and binds to DNA dependent on the formation of DNA stem-loop structures. 5-Methyl-2'-deoxycytidine guides de novo DNA methylation by acting as a methylation mark and activates the methylation of adjacent CpG sites in single-stranded DNA through cis action. 5-Methyl-2'-deoxycytidine regulates DNA methylation patterns by recruiting methyltransferases to specific chromatin regions, affecting chromatin condensation and gene expression. Its distribution in plant cells is related to cell proliferation and differentiation stages. The methylation level of 5-Methyl-2'-deoxycytidine is low in proliferating cells and high in differentiated cells .
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2
2 Cited Publications
Art. -Nr.: HY-113047
CAS. Nr.: 5627-05-4
Reinheit:  99.58%
5,6-Dihydrouridine is a modified base found in conserved positions in the D-loop of tRNA in Bacteria, Eukaryota, and some Archaea.
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2
2 Cited Publications
Art. -Nr.: HY-13242
CAS. Nr.: 1258861-20-9
Reinheit:  99.92%
Synonyms: LY2940680
Target:  

Smo Gli

Forschungsgebiete:  

Cancer

Taladegib is a Smoothened (SMO) antagonist. Taladegib hydrochloride inhibits the Hedgehog signaling pathway, with an IC50 of 5.5 nM for suppressing GLI1 mRNA expression in DAOY cells and an IC50 of 7.6 nM in CGNP cell proliferation assays. Taladegib binds to the extracellular loop region (site 1) of the transmembrane domain of the SMO receptor, competes with cyclopamine for SMO binding, and thereby inhibits Gli-dependent transcription. Taladegib can be used in studies of Hedgehog pathway-related cancers .
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