296 Results for "

F1

" in MedChemExpress (MCE) Product Catalog:
Products (296)

296 Results for "F1" in MCE Product Catalog:

製品番号: HY-112801
CAS 番号: 2244775-31-1
純度:  98.03%
研究分野:  

Cancer

F-1 is a potent ALK and ROS1 dual inhibitor, suppresses phospho-ALK and its relative downstream signaling pathways, with IC50s of 2.1 nM, 2.3 nM, 1.3 nM and 3.9 nM for ALK WT, ROS1 WT, ALK L1196M and ALK G1202R, respectively [1].
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61
61 Publications Verification
製品番号: HY-16589
CAS 番号: 579-13-5
別名: MCH 32
Oligomycin A (MCH 32), created by Streptomyces, acts as a mitochondrial F0F1-ATP synthase inhibitor, with a Ki of 1 μM; Oligomycin A shows anti-fungal activity.
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59
59 Cited Publications
製品番号: HY-14881
CAS 番号: 843663-66-1
純度:  99.98%
別名: TMC207; R207910
Target:  

Bacterial Antibiotic

研究分野:  

Infection

Bedaquiline (TMC207) is a diarylquinoline agent and inhibits Mycobacterium tuberculosis (Mtb) F1FO-ATP synthase through targeting of both the c- and the ε-subunit [1]. Bedaquiline has uncoupler activity. Bedaquiline is used for the multi-agent resistant tuberculosis .
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7
7 Cited Publications
製品番号: HY-111651
CAS 番号: 2101315-36-8
純度:  98.23%
Gboxin is an oxidative phosphorylation (OXPHOS) inhibitor that targets glioblastoma. Gboxin inhibits the activity of F0F1 ATP synthase. Antitumour activity [1].
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5
5 Cited Publications
製品番号: HY-P7027
純度:  ≥ 95%, as determined by reducing SDS-PAGE.
別名: IL1A; IL-1A; Prev. IL1; Preinterleukin 1 Alpha; IL1F1; Interleukin-1 Alpha; Hematopoietin-1; IL-1 Alpha; IL1-ALPHA; Interleukin 1 Alpha; Pro-Interleukin-1-Alpha
Species:  
Human
Source:  
E. coli
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4
4 Cited Publications
製品番号: HY-P7072
純度:  ≥ 95%, as determined by reducing SDS-PAGE.
別名: IL1A; IL-1A; Prev. IL1; Preinterleukin 1 Alpha; IL1F1; Interleukin-1 Alpha; Hematopoietin-1; IL-1 Alpha; IL1-ALPHA; Interleukin 1 Alpha; Pro-Interleukin-1-Alpha
Species:  
Mouse
Source:  
E. coli
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3
3 Cited Publications
製品番号: HY-P7054
純度:  ≥ 95%, as determined by reducing SDS-PAGE.
別名: SERPINF1; Testis Tissue Sperm-Binding Protein Li 70n; Prev. PEDF; Serpin Peptidase Inhibitor, Clade F (Alpha-2 Antiplasmin, Pigment Epithelium Derived Factor), Member 1; EPC-1; Proliferation-Inducing Protein 35; Pigment Epithelium-Derived Factor; Serpin F
Species:  
Human
Source:  
E. coli
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3
3 Cited Publications
製品番号: HY-118155
CAS 番号: 3548-09-2
純度:  99.56%
別名: ACMA
9-Amino-6-chloro-2-methoxyacridine (ACMA) is an acridine derivative and Fluorescent probe. 9-Amino-6-chloro-2-methoxyacridine inhibits viral replication, inhibits DNA synthesis and protein metabolism through cell cycle arrest, and induces lipid metabolism regulation, genotoxicity, mutagenicity, and cytotoxicity through DNA strand breaks. 9-Amino-6-chloro-2-methoxyacridine partially intercalates into DNA, forming three distinct complexes, stabilizes the DNA helix, and quenches fluorescence upon intercalation through electron transfer with guanine. 9-Amino-6-chloro-2-methoxyacridine monitors the generation and collapse of the proton motive force, H + pumping by F1F0-ATP synthase, and the collapse of pH gradients in inverted membrane vesicles. 9-Amino-6-chloro-2-methoxyacridine shows potent anti-BVDV activity. 9-Amino-6-chloro-2-methoxyacridine can be used for research on bovine viral diarrhea virus infection, leishmaniasis, and MRSA infection [1] .
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2
2 Cited Publications
製品番号: HY-N0598
CAS 番号: 53963-43-2
別名: 20(S)-Ginsenoside F1
Ginsenoside F1, an enzymatically modified derivative of Ginsenoside Rg1, demonstrates competitive inhibition of CYP3A4 activity and weaker inhibition of CYP2D6 activity.
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2
2 Cited Publications
製品番号: HY-17355A
CAS 番号: 104632-27-1
別名: (R)-Pramipexole dihydrochloride; R-(+)-Pramipexole dihydrochloride; KNS-760704 dihydrochloride
Dexpramipexole ((R)-Pramipexole) dihydrochloride is an orally active, blood-brain barrier permeable mitochondrial protective agent. Dexpramipexole dihydrochloride upregulates the expression of Parkin, PINK1, GPX4 and FSP1; binds to mitochondrial F1/Fo-ATP synthase; blocks the Nav1.8 sodium channel; and inhibits the activation of the NLRP3 inflammasome. Dexpramipexole dihydrochloride induces mitophagy, inhibits ferroptosis, pyroptosis, apoptosis, neuroinflammation and eosinophilopoiesis; maintains mitochondrial function and redox homeostasis; reduces reactive oxygen species production; and decreases myocardial infarct size. Dexpramipexole dihydrochloride is applicable to studies on eosinophilic asthma, myocardial ischemia/reperfusion injury, sepsis-associated encephalopathy, analgesia, and more [1] .
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2
2 Cited Publications
製品番号: HY-17355B
CAS 番号: 104632-28-2
別名: (R)-Pramipexole; R-(+)-Pramipexole; KNS-760704
Dexpramipexole ((R)-Pramipexole) is an orally active, blood-brain barrier permeable mitochondrial protective agent. Dexpramipexole upregulates the expression of Parkin, PINK1, GPX4 and FSP1; binds to mitochondrial F1/Fo-ATP synthase; blocks the Nav1.8 sodium channel; and inhibits the activation of the NLRP3 inflammasome. Dexpramipexole induces mitophagy, inhibits ferroptosis, pyroptosis, apoptosis, neuroinflammation and eosinophilopoiesis; maintains mitochondrial function and redox homeostasis; reduces reactive oxygen species production; and decreases myocardial infarct size. Dexpramipexole is applicable to studies on eosinophilic asthma, myocardial ischemia/reperfusion injury, sepsis-associated encephalopathy, analgesia, and more [1] .
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2
2 Cited Publications
製品番号: HY-P99364
CAS 番号: 1024603-92-6
別名: Anti-VEGFR1/FLT1 Reference Antibody; IMC-18F1

Target:  

VEGFR Apoptosis p38 MAPK Akt

研究分野:  

Endocrinology Cancer

Icrucumab (Anti-VEGFR1/FLT1 Reference Antibody; IMC-18F1) is an IgG1 antibody inhibitor targeting VEGFR-1/FLT1 with anti-tumor activity. By blocking ligand-dependent phosphorylation and downstream signal transduction, Icrucumab reduces the activities of MAPK and Akt in breast cancer xenograft models, inhibits the proliferation and invasion of VEGFR-1-positive tumor cells, and reverses the conversion of M1 macrophages to the pro-tumor M2-like phenotype. Icrucumab also inhibits tumor cell proliferation, promotes apoptosis, and effectively suppresses tumor growth through direct targeting of tumors and host support mechanisms. In addition, Icrucumab exhibits a synergistic effect when combined with chemotherapeutic agents, and it is used in research related to various cancers including advanced solid malignancies, thyroid cancer, melanoma, and lung cancer [1] .
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2
2 Cited Publications
製品番号: HY-15877
CAS 番号: 219793-45-0
純度:  99.60%
Target:  

ATP Synthase

研究分野:  

Cancer

BTB06584 is a selective and IF1-dependent mitochondrial F1Fo-ATPase inhibitor without compromising ATP synthesis. BTB06584 can delays ischaemic cell death [1].
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2
2 Cited Publications
製品番号: HY-P79451
純度:  ≥ 95%, as determined by reducing SDS-PAGE.
別名: UBE2L3; Ubiquitin Conjugating Enzyme E2 L3; UBCH7; Ubiquitin-Conjugating Enzyme E2 L3; E2 Ubiquitin-Conjugating Enzyme L3; Ubiquitin-Conjugating Enzyme E2-F1; Ubiquitin Carrier Protein L3; Ubiquitin-Protein Ligase L3; L-UBC; Ubiquitin-Conjugating Enzyme E
Species:  
Human
Source:  
E. coli
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1
1 Cited Publications
製品番号: HY-149913
CAS 番号: 374101-64-1
純度:  99.83%
研究分野:  

Cancer

NR2F1 agonist 1, a nuclear receptor NR2F1 agonist, specifically activates dormancy programs in malignant cells. NR2F1 agonist 1 up-regulates NR2F1 and downstream target genes that regulate dormancy. NR2F1 agonist 1 induces neural crest-like and growth suppression in head and neck squamous cell carcinoma (HNSCC) via NR2F1 activation. NR2F1 agonist 1 inhibits tumor growth in a mouse primary tumor model [1].
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1
1 Cited Publications
製品番号: HY-P73372
純度:  ≥ 95%, as determined by reducing SDS-PAGE.
別名: SERPINF1; Testis Tissue Sperm-Binding Protein Li 70n; Prev. PEDF; Serpin Peptidase Inhibitor, Clade F (Alpha-2 Antiplasmin, Pigment Epithelium Derived Factor), Member 1; EPC-1; Proliferation-Inducing Protein 35; Pigment Epithelium-Derived Factor; Serpin F
Species:  
Mouse
Source:  
HEK293
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1
1 Cited Publications
製品番号: HY-P70498A
純度:  ≥ 95%, as determined by reducing SDS-PAGE.
別名: SERPINF1; Testis Tissue Sperm-Binding Protein Li 70n; Prev. PEDF; Serpin Peptidase Inhibitor, Clade F (Alpha-2 Antiplasmin, Pigment Epithelium Derived Factor), Member 1; EPC-1; Proliferation-Inducing Protein 35; Pigment Epithelium-Derived Factor; Serpin F
Species:  
Human
Source:  
HEK293
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1
1 Cited Publications
製品番号: HY-113358
CAS 番号: 58962-34-8
6-keto Prostaglandin F1α is an endogenous metabolite present in Cerebrospinal_Fluid, Urine and Blood that can be used for the research of Meningitis, Rheumatoid Arthritis and Cardiopulmonary Resuscitation [1] .
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1
1 Cited Publications
製品番号: HY-N4165
CAS 番号: 6750-30-7
Arnidiol is a pentacyclic triterpene isolated from Barleria Longiflora Linn F. .
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1
1 Cited Publications
製品番号: HY-N2253
CAS 番号: 17676-33-4
Neoruscogenin, a member of the steroidal sapogenin family, is a high-affinity agonist of the nuclear receptor RORα (NR1F1) (EC50 = 0.11 µM) [1].
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