11 Results for "

mitogenesis

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "mitogenesis" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-21290
CAS No.: 76086-99-2
Target:  

Tyrosinase

Research Areas:  

Cancer

SU-4942 is a tyrosine kinase signal signal modulator. SU-4942 inhibits VEGF- and endothelial cell growth factor (ECGF)-induced mitogenesis in endothelial cells (US5792783A) .
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Cat. No.: HY-12697
CAS No.: 189060-98-8
Purity:  98.28%
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

NGB 2904 is a potent, selective, orally active and brain-penetrated antagonist of dopamine D3 receptor, with a Ki of 1.4 nM. NGB 2904 shows selectivity for D3 over D2, 5-HT2, α1, D4, D1 and D5 receptors (Kis=217, 223, 642, >5000, >10000 and >10000 nM, respectively). NGB 2904 antagonizes Quinpirole-stimulated mitogenesis .
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Cat. No.: HY-21289
CAS No.: 3476-86-6
Target:  

VEGFR

Research Areas:  

Cancer

SU5205 is an inhibitor of VEGFR2 (FLK-1), with an IC50 of 9.6 μM .
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Cat. No.: HY-116111
CAS No.: 134036-53-6
Purity:  ≥97.0%
Target:  

PDGFR

Research Areas:  

Cardiovascular Disease

AG 370, an indole tyrphostin, is a potent PDGF-induced mitogenesis inhibotor (IC50 of 20 μM). AG 370 displays weak inhibition of the EGF receptor .
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Cat. No.: HY-111006
CAS No.: 95999-12-5
Synonyms: UH 232
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

(+)-UH 232 is a partially selective agonist of the D3 receptor with an intrinsic activity of 0.2-0.4. (+)-UH 232 antagonized quinpirole-induced mitogenesis with a Ki value of 9.4 nM .
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Cat. No.: HY-12697A
CAS No.: 189061-11-8
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

NGB 2904 hydrochloride is a potent, selective, orally active and brain-penetrated antagonist of dopamine D3 receptor, with a Ki of 1.4 nM. NGB 2904 hydrochloride shows selectivity for D3 over D2, 5-HT2, α1, D4, D1 and D5 receptors (Kis=217, 223, 642, >5000, >10000 and >10000 nM, respectively). NGB 2904 hydrochloride antagonizes Quinpirole-stimulated mitogenesis .
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Cat. No.: HY-174686
Target:  

mRNA

Research Areas:  

Cancer

Human FGFRL1 mRNA encodes the human fibroblast growth factor receptor like 1 (FGFRL1) protein, a member of the fibroblast growth factor receptor (FGFR) family. The extracellular portion of FGFRL1 protein can interact with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation.
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Cat. No.: HY-174689
Target:  

mRNA

Research Areas:  

Cancer

Human FGFR2 mRNA encodes the human fibroblast growth factor receptor 2 (FGFR2) protein, a member of the fibroblast growth factor receptor (FGFR) family. The extracellular portion of FGFR2 protein can interact with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation.
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Cat. No.: HY-174690
Target:  

mRNA

Research Areas:  

Cancer

Human FGFR1 mRNA encodes the human fibroblast growth factor receptor 1 (FGFR1) protein, a member of the fibroblast growth factor receptor (FGFR) family. The extracellular portion of FGFR1 protein can interact with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation.
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Cat. No.: HY-174688
Target:  

mRNA

Research Areas:  

Cancer

Human FGFR3 mRNA encodes the human fibroblast growth factor receptor 3 (FGFR3) protein, a member of the fibroblast growth factor receptor (FGFR) family. The extracellular portion of FGFR3 protein can interact with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation.
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Cat. No.: HY-135446
CAS No.: 141595-53-1
Target:  

Endothelin Receptor

BQ-610 is a selective antagonist of the endothelin A receptor (ETA receptor). BQ-610 specifically blocks the ETA receptor, competitively inhibiting the binding of endothelin-1 (ET-1) (a vasoconstrictive peptide) to the receptor, thereby blocking the effects of ET-1 such as vascular smooth muscle contraction, cell mitosis, and inhibition of hormone secretion. BQ-610 significantly alleviates cerebral vasospasm in rabbits. BQ-610 blocks the bronchial epithelial and pulmonary vascular cell proliferation caused by cigarette smoke in rat models. BQ-610 can delay the natural luteal regression in the cow's uterus. BQ-610 can be used for research on vasospasm, abnormal cell proliferation, and reproductive endocrine disorders .
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