141 Results for "

PDGF

" in MedChemExpress (MCE) Product Catalog:
Products (141)

141 Results for "PDGF" in MCE Product Catalog:

  • Recombinant Proteins Recommended:
28
28 Cited Publications
Cat. No.: HY-P7055
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHuPDGF-BB; PDGF-2; GDGF; ODGF; SIS; SSV
Species:  
Source:  
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12
12 Cited Publications
Cat. No.: HY-P7278
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rRtPDGF-BB; PDGF-2; PDGFb
Species:  
Rat
Source:  
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9
9 Cited Publications
Cat. No.: HY-P7087
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rMuPDGF-BB; PDGF-2; GDGF; ODGF; SIS; SSV
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8
8 Cited Publications
Cat. No.: HY-N0284
CAS No.: 305-01-1
Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities .
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6
6 Cited Publications
Cat. No.: HY-N0590
CAS No.: 630-94-4
Corynoxeine, isolated from the hook of Uncaria rhynchophylla, is a potent ERK1/ERK2 inhibitor of key PDGF-BB-induced vascular smooth muscle cells (VSMCs) proliferation.
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3
3 Cited Publications
Cat. No.: HY-N0366
CAS No.: 128-57-4
Sennoside B is a potent and orally active platelet-derived growth factor (PDGF) inhibitor. Sennoside B inhibits cell proliferation and the expression of phosphorylation of PDGFR-β, STAT-5, AKT and ERK induced by PDGF-BB. Sennoside B shows gastroprotective activities. Sennoside B has the potential for the research of gastritis .
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3
3 Cited Publications
Cat. No.: HY-13894
CAS No.: 146535-11-7
Purity:  99.69%
Synonyms: AG1296
Tyrphostin AG1296 is a potent and selective inhibitor of platelet-derived growth factor receptor (PDGFR), with an IC50 of 0.8 μM. Tyrphostin AG1296 inhibits signaling of human PDGF α- and β-receptors as well as of the related stem cell factor receptor (c-Kit). Tyrphostin AG1296 is also a potent inhibitor of FLT3, with an IC50 in the micromolar range .
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3
3 Cited Publications
Cat. No.: HY-P7280
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHuPDGF-DD; Platelet-derived growth factor D; SCDGFB
Species:  
Source:  
CHO
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2
2 Cited Publications
Cat. No.: HY-P70598
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: PDGFAA; PDGF-AA
Species:  
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2
2 Cited Publications
Cat. No.: HY-P7279
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHuPDGF-CC; PDGF-C; SCDGF
Species:  
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2
2 Cited Publications
Cat. No.: HY-N2484
CAS No.: 73340-41-7
Synonyms: Astrapterocarpan
Methylnissolin (Astrapterocarpan) is an osteoclast inhibitor with anti-inflammatory, neuroprotective and antioxidant activities. Methylnissolin downregulates the activation of the MAPK and PI3K/AKT pathways, inhibits the phosphorylation of MAPK1 and AKT1, and blocks PDGF-BB-induced phosphorylation of ERK1/2. Methylnissolin reduces the expression and secretion of proinflammatory mediators, decreases intracellular ROS levels, upregulates antioxidant enzymes, and downregulates osteoclastogenesis markers. Methylnissolin is applicable to research related to ischemic stroke, osteoporosis, cardiovascular diseases, skin aging, etc.
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1
1 Cited Publications
Cat. No.: HY-10527
CAS No.: 332012-40-5
Purity:  99.37%
Synonyms: Bay 57-9352
Target:  

c-Kit PDGFR VEGFR

Research Areas:  

Cancer

Telatinib (Bay 57-9352) is an orally active, small molecule inhibitor of VEGFR2, VEGFR3, PDGFα, and c-Kit with IC50s of 6, 4, 15 and 1 nM, respectively.
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1
1 Cited Publications
Cat. No.: HY-10527C
CAS No.: 332013-26-0
Purity:  99.74%
Synonyms: Bay 57-9352 mesylate
Target:  

VEGFR PDGFR c-Kit

Research Areas:  

Cancer

Telatinib mesylate (Bay 57-9352 mesylate) is a potent and orally active VEGFR2, VEGFR3, PDGFα, and c-Kit inhibitor with IC50s of 6 nM, 4 nM, 15 nM and 1 nM, respectively .
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1
1 Cited Publications
Cat. No.: HY-P7055B
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHuPDGF-BB; PDGF-2; GDGF; ODGF; SIS; SSV
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-P7055A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHuPDGF-BB; PDGF-2; GDGF; ODGF; SIS; SSV
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-P7055G
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: PDGFBB; PDGF-BB
Species:  
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1
1 Cited Publications
Cat. No.: HY-P73351
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Platelet-derived growth factor subunit B; PDGF subunit B; PDGF2; PDGFB; SIS
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-W011266
CAS No.: 627518-40-5
Target:  

PDGFR

Research Areas:  

Cancer

JNJ-10198409 is a relatively selective, orally active, and ATP competitive PDGF-RTK (platelet-derived growth factor receptor tyrosine kinase) inhibitor (IC50=2 nM). It is a dual-mechanism, antiangiogenic, and tumor cell antiproliferative agent. JNJ-10198409 has good activity against PDGFR-β kinase (IC50=4.2 nM) and PDGFR-α kinase (IC50=45 nM) .
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1
1 Cited Publications
Cat. No.: HY-133708
CAS No.: 13405-60-2
Purity:  99.82%
Synonyms: Glucogallin; 1-O-Galloyl-β-D-glucose
β-Glucogallin is an orally active and selective aldose reductase (AKR1B1) inhibitor with an IC50 value of 58 μM when using Glyceraldehyde (HY-128748) as AKR1B1 substrate. β-Glucogallin reduces ROS, PDGF, RAGE, and NF-κB. β-Glucogallin increases SOD. β-Glucogallin has antioxidant and hepatoprotective effects. β-Glucogallin can be used in retinal research .
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1
1 Cited Publications
Cat. No.: HY-N2464
CAS No.: 34612-38-9
Synonyms: Amylotetraose; Fujioligo 450; α-1,4-Tetraglucose
Maltotetraose can serve as a substrate for enzyme-linked assays to measure amylase activity in biological fluids. Maltotetraose has oral active, and reduces TNF-α-induced inflammatory responses by inhibiting NF-κB activity and decreasing ICAM-1 expression. Maltotetraose also inhibits PDGF-induced vascular smooth muscle cell migration and neovascularization. Additionally, Maltotetraose derivatives can function as probes for detecting bacterial infections by targeting the maltodextrin transporter. With good long-term safety, Maltotetraose holds promise for research in atherosclerosis-related diseases .
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