66 Results for "

transforming-growth-factor-&beta

" in MedChemExpress (MCE) Product Catalog:
Products (66)

66 Results for "transforming-growth-factor-&beta" in MCE Product Catalog:

22
22 Publications Verification
Cat. No.: HY-13012
CAS No.: 446859-33-2
Purity:  99.92%
Synonyms: E-616452; SJN 2511
Research Areas:  

Metabolic Disease

RepSox (E-616452) is a potent and selective transforming growth factor-beta receptor I/activin like kinase 5 (TGF-β-RI/ALK5) inhibitor. RepSox inhibits ALK5 autophosphorylation with an IC50 value of 4 nM. RepSox can be used for the research of obesity and associated metabolic diseases such as type 2 diabetes .
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19
19 Cited Publications
Cat. No.: HY-P0118B
Synonyms: P144 diammonium
Research Areas:  

Cancer

Disitertide (P144) diammonium is a peptidic transforming growth factor-beta 1 (TGF-β1) inhibitor specifically designed to block the interaction with its receptor. Disitertide diammonium is also a PI3K inhibitor and an apoptosis inducer .
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19
19 Cited Publications
Cat. No.: HY-P0118
CAS No.: 272105-42-7
Synonyms: P144
Research Areas:  

Cancer

Disitertide (P144) is a peptidic transforming growth factor-beta 1 (TGF-β1) inhibitor specifically designed to block the interaction with its receptor. Disitertide (P144) is also a PI3K inhibitor and an apoptosis inducer .
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5
5 Cited Publications
Cat. No.: HY-P99720
CAS No.: 1373715-00-4
Synonyms: ACE-536; luspatercept–aamt

Target:  

TGF-beta/Smad

Research Areas:  

Cardiovascular Disease

Luspatercept (ACE-536) is a recombinant modified ActRIIB fusion protein that binds with transforming growth factor β superfamily ligands. Luspatercept increases the erythrocyte numbers and promotes maturation of erythroid precursors. Luspatercept binds with GDF11 and inhibits Smad2/3 signaling. Luspatercept can be used for the research of anemia .
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3
3 Cited Publications
Cat. No.: HY-112331
CAS No.: 425613-09-8
Purity:  99.66%
Target:  

TGF-β Receptor

Research Areas:  

Cancer

SJ000291942 is an activator of the canonical bone morphogenetic proteins (BMP) signaling pathway. BMPs are members of the transforming growth factor beta (TGFβ) family of secreted signaling molecules.
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3
3 Cited Publications
Cat. No.: HY-115669
CAS No.: 69640-38-6
Purity:  98.88%
Synonyms: Antibiotic A 15104 Y; PClP
Target:  

Myosin TGF-β Receptor

Research Areas:  

Cancer

Pentachloropseudilin (Antibiotic A 15104 Y; PClP) is a reversible and allosteric potent inhibitor of Myo1s (class 1 myosins) with IC50s range from 1 to 5 μM for mammalian class-1 myosins and greater than 90 μM for class-2 and class-5 myosins. Pentachloropseudilin is a potent inhibitor of transforming growth factor-β (TGF-β)-stimulated signaling, with an IC50 of 0.1 to 0.2 μM for TGF-β .
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2
2 Cited Publications
Cat. No.: HY-18758
CAS No.: 868612-83-3
Target:  

TGF-β Receptor

Research Areas:  

Inflammation/Immunology Cancer

IN-1130 is a highly selective transforming growth factor-β type I receptor kinase (ALK5) inhibitor with an IC50 of 5.3 nM for ALK5-mediated Smad3 phosphorylation. IN-1130 inhibits ALK5 phosphorylation of casein (IC50=36 nM) and p38α mitogen-activated protein kinase (IC50=4.3 μM). IN-1130 suppresses renal fibrosis in obstructive nephropathy and blocks breast cancer lung metastasis .
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1
1 Cited Publications
Cat. No.: HY-128437
CAS No.: 259870-32-1
Purity:  98.03%
Target:  

TGF-β Receptor

Research Areas:  

Inflammation/Immunology

TGFβ-IN-5 is a type I transforming growth factor-β receptor (TGF-β R1) kinase inhibitor with an IC50 value of 0.0485 μM. TGFβ-IN-5 reverses the effect of TGF-β-mediated cell activation on the expression of fibrosis-related genes. TGFβ-IN-5 can be used in the research of fibroproliferative diseases .
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1
1 Cited Publications
Cat. No.: HY-113604
CAS No.: 10245-81-5
Purity:  99.63%
Pentabromopseudilin (PBrP) is a marine antibiotic isolated from the marine bacteria Pseudomonas bromoutilis and Alteromonas luteoviolaceus. PBrP exhibits antimicrobial, anti-tumour and phytotoxic activities. PBrP is a reversible and allosteric inhibitor of myosin Va (MyoVa). PBrP also is a potent inhibitor of transforming growth factor-β (TGF-β) activity. PBrP can be used for the research of fibrotic diseases and cancer .
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1
1 Cited Publications
Cat. No.: HY-P74525A
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: transforming growth factor-beta-induced protein ig-h3; Beta ig-h3; RGD-CAP; BIGH3
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-P80908
Synonyms: MAP3K7; TAK1; Mitogen-activated protein kinase kinase kinase 7; transforming growth factor-beta-activated kinase 1; TGF-beta-activated kinase 1

Host:  

Mouse

Application:  

WB

Reactivity:  

Human, Mouse, Rat, Monkey

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1
1 Cited Publications
Cat. No.: HY-P80858
Synonyms: MAP3K7; TAK1; Mitogen-activated protein kinase kinase kinase 7; transforming growth factor-beta-activated kinase 1; TGF-beta-activated kinase 1

Host:  

Rabbit

Application:  

WB, ICC/IF, IP

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-112671
CAS No.: 1191265-33-4
Purity:  99.71%
Synonyms: RTA dh404
CDDO-dhTFEA (RTA dh404) is a synthetic oleanane triterpenoid compound which potently activates Nrf2 and inhibits the pro-inflammatory transcription factor NF-κB . CDDO-dhTFEA restores hypertension (MAP), increases Nrf2 and expression of its target genes, attenuates activation of NF-κB and transforming growth factor-β pathways, and reduces glomerulosclerosis, interstitial fibrosis and inflammation in the chronic kidney disease (CKD) rats .
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Cat. No.: HY-13783
CAS No.: 334951-90-5
Purity:  99.42%
Target:  

TGF-β Receptor

Research Areas:  

Cancer

BIBF0775 is a potent and selective transforming growth factor β (TGFβ) type I receptor (Alk5) inhibitor with an IC50 of 34 nM.
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Cat. No.: HY-120548
CAS No.: 1143863-69-7
Purity:  99.52%
Research Areas:  

Cancer

KBU2046 is an orally active transforming growth factor-β (TGF-β1) inhibitor. KBU2046 reduces integrin family protein expression, decreases Raf, RIPK1 and ERK phosphorylation to deactivate the ERK signaling pathway, and down-regulates genes linked to TGF-β1 maturation. KBU2046 suppresses tumor cell motility, impedes cancer invasion and metastasis, and inhibits human ESCC growth and metastasis in a murine model. KBU2046 can be used for the researches of triple-negative breast cancer and esophageal squamous cell carcinoma .
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Cat. No.: HY-P5189A
Research Areas:  

Others

His-D-beta-Nal-Ala-Trp-D-Phe-Lys-NH2 TFA, is a growth hormone releasing peptide, as well as a metabolite of GHRP-1. GHRP-1, or Ala-His-D-beta Nal-Ala-Trp-D-Phe-Lys-NH2, has the effect of promoting the release of growth hormone (GH). GHRP-1 increases GH release and increases [Ca2+]i levels in static monolayer cells of rat pituitary gland, but does not affect cAMP levels .
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Cat. No.: HY-146693
CAS No.: 1807631-83-9
Purity:  99.36%
Target:  

TGF-β Receptor

Research Areas:  

Cancer

CJJ300 is a transforming growth factor-β (TGF-β) inhibitor with an IC50 of 5.3 µM. CJJ300 inhibits TGF-β signaling by disrupting the formation of the TGF-β-TβR-I-TβR-II signaling complex .
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Cat. No.: HY-W105318
CAS No.: 608-71-9
Synonyms: PBP
Target:  

TGF-beta/Smad Apoptosis

Research Areas:  

Cancer

Pentabromophenol (PBP) is a brominated flame retardant (BFR) widely used in various consumer products to reduce the flammability of materials used in different utility items. Pentabromophenol can accelerate the degradation of transforming growth factor-β (TGF-β) receptors by promoting clathrin-mediated endocytosis, thereby inhibiting the TGF-β signaling pathway. Additionally, Pentabromophenol can also induce apoptosis in peripheral blood mononuclear cells (PBMCs) .
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Cat. No.: HY-P5457
CAS No.: 500719-13-1
Target:  

Peptides

Research Areas:  

Others

BMP-2 Epitope (73-92) is a biological active peptide. (This is amino acids 73 to 92 fragment of bone morphogenetic protein (BMP) knuckle epitope. It is a member of transforming growth factor beta (TGF-b). This peptide fragment is able to raise alkaline phosphate activity in murine multipotent mesenchymal cells.)
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Cat. No.: HY-142967
CAS No.: 883560-84-7
Target:  

TGF-β Receptor

Research Areas:  

Cancer

TGFβ-IN-1 is an antitumor growth and metastasis agent through inhibiting the transforming growth factor‑β signaling pathway.
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