359 Results for "

FGF

" in MedChemExpress (MCE) Product Catalog:
Products (359)

359 Results for "FGF" in MCE Product Catalog:

43
43 Publications Verification
Cat. No.: HY-P7004
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHubFGF; HBGF-2; FGF-2; FGF-b; FGF-basic
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14
14 Cited Publications
Cat. No.: HY-P7066
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rMubFGF; HBGF-2; FGF-2; FGF-b; FGF-basic
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12
12 Cited Publications
Cat. No.: HY-P7014
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHuFGF-4; HBGF-4; HST; HST-1; HSTF1
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9
9 Cited Publications
Cat. No.: HY-101568
CAS No.: 1708971-55-4
Purity:  99.67%
Synonyms: FGF-401
Target:  

FGFR

Research Areas:  

Cancer

Roblitinib (FGF-401) is an orally active and highly selective FGFR4 inhibitor with an IC50 of 1.9 nM . Roblitinib has antitumor activity .
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9
9 Cited Publications
Cat. No.: HY-P7331
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHubFGF, 154a.a.; bFGF; FGF-2; HBGF-2; FGFB
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5
5 Cited Publications
Cat. No.: HY-P7091
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rRtbFGF; HBGF-2; FGF-2; FGF-b; FGF-basic
Species:  
Rat
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5
5 Cited Publications
Cat. No.: HY-P7170
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rMuFGF-10; Keratinocyte growth factor-2; FGF10
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5
5 Cited Publications
Cat. No.: HY-P701242
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Fibroblast growth factor 2; FGF-2; Basic fibroblast growth factor; bFGF; Heparin-binding growth factor 2; HBGF-2; FGF2; FGFB
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4
4 Cited Publications
Cat. No.: HY-P7173
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rMuFGF-21; FGF21
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4
4 Cited Publications
Cat. No.: HY-P70473
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Fibroblast Growth Factor 21; FGF-21; FGF21
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4
4 Cited Publications
Cat. No.: HY-P7330
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHubFGF, 145a.a.; bFGF; FGF-2; HBGF-2; FGFB
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4
4 Cited Publications
Cat. No.: HY-P1408
CAS No.: 404882-00-4
Target:  

Integrin VEGFR

Research Areas:  

Cancer

Obtustatin is a non-RGD disintegrin consisting of 41 residues. Obtustatin inhibits the adhesion of α1β1 integrin to type IV Collagen (HY-NP003), blocks α1β1 integrin signaling in endothelial cells, and suppresses FGF2-induced angiogenesis. Obtustatin inhibits tumor progression in mouse models and upregulates VEGF expression in sarcoma-bearing mice. Obtustatin can be used in research related to Lewis lung carcinoma and S-180 sarcoma .
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4
4 Cited Publications
Cat. No.: HY-P70597
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Fibroblast growth factor 7; FGF-7; Heparin-binding growth factor 7; HBGF-7; Keratinocyte growth factor; FGF7; KGF
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4
4 Cited Publications
Cat. No.: HY-107574
CAS No.: 17328-16-4
Purity:  98.03%
TC-E 5003 is a selective protein arginine methyltransferase 1 (PRMT1) inhibitor with an IC50 of 1.5 µM against hPRMT1. TC-E 5003 modulates the lipopolysaccharide (LPS) (HY-D1056)-induced AP-1 and NF-κB signaling pathways with anti-inflammatory properties. TC-E 5003 also upregulates the expression of Ucp1 and Fgf21, activates protein kinase A signaling and lipolysis in primary subcutaneous adipocytes from both mouse and humans. TC-E 5003 is promising for research of obesity and associated metabolic disorders, oxidative stress, inflammation and cancers .
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3
3 Cited Publications
Cat. No.: HY-P72651
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: FGF21; Fibroblast Growth Factor 21; FGF-21
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3
3 Cited Publications
Cat. No.: HY-P73052
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Fibroblast growth factor 2; FGF-2; bFGF; HBGF-2; FGF2
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3
3 Cited Publications
Cat. No.: HY-P7331A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHubFGF, 154a.a.; bFGF; FGF-2; HBGF-2; FGFB
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3
3 Cited Publications
Cat. No.: HY-P70533
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Fibroblast growth factor 8; Androgen-induced growth factor; Heparin-binding growth factor 8; AIGF; HBGF-8; FGF-8B
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3
3 Cited Publications
Cat. No.: HY-108628
CAS No.: 251356-45-3
Purity:  99.36
Target:  

PDGFR

Research Areas:  

Cancer

SU16f is a potent and selective PDGFRβ inhibitor with IC50s of 10 nM, 140 nM, 2.29 μM for PDGFRβ, VEGF-R2, FGF-R1, respectively . Neutralization of PDGFRβ receptor by SU16f blocks the promoting role of GC-MSCs (gastric cancer-derived mesenchymal stem cells) conditioned medium in gastric cancer cell proliferation and migration .
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2
2 Cited Publications
Cat. No.: HY-148432
CAS No.: 113143-13-8
Purity:  98.07%
Target:  

HIV

Research Areas:  

Inflammation/Immunology

FGF22-IN-1 (compound c1) is a potent CD4 D1 inhibitor. FGF22-IN-1 can be used as immunosuppressive agent .
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