8 Results for "

dwarfism

" in MedChemExpress (MCE) Product Catalog:
Products (8)

8 Results for "dwarfism" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-121161A
CAS No.: 280129-83-1
Purity:  99.71%
Target:  

Cytochrome P450

Research Areas:  

Others

Brassinazole is a selective triazole-type brassinosteroid (BR) biosynthesis inhibitor. Brassinazole is used for regulating plant growth and development .
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Cat. No.: HY-P3503
CAS No.: 1480724-61-5
Synonyms: BMN 111
Target:  

FGFR

Research Areas:  

Others

Vosoritide (BMN 111) is a modified recombinant CNP (C-type natriuretic peptide) analogue, binds to NPR-B (natriuretic peptide receptor type B) and reduces the activity of FGFR3 (fibroblast growth factor receptor 3). Vosoritide can be used in achondroplasia and dwarfism research .
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Cat. No.: HY-121161C
CAS No.: 259200-30-1
Purity:  99.83%
Target:  

Phytohormone

Research Areas:  

Metabolic Disease

Brassinazole (0.5, 1, 5 μM) causes markedly deformed seedlings, whose morphology is similar to that of BR-deficient mutants. Brassinazole causes cress dwarfism, altering leaf morphology such as the typical downward curl and dark green appearance of Arabidopsis BR-deficient mutants. However, administration of 10 nM BR reversed dwarfism .
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Cat. No.: HY-115707
CAS No.: 126281-90-1
Synonyms: 16:0/0:0/18:3-DG; DG(16:0/0:0/18:3); 1-Palmitin-3-Linolenin
Target:  

Others

Research Areas:  

Others

1-Palmitoyl-3-Linolenoyl-rac-glycerol (16:0/0:0/18:3-DG) is a diacylglycerol containing palmitic acid (HY-N0830) and α-linolenic acid (HY-N0728) at the sn-1 and sn-3 positions, respectively. It has been found in the peel and pulp of unripe Dwarf Cavendish bananas.
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Cat. No.: HY-P5129
Target:  

Peptides

Research Areas:  

Others

ASB20123 is a CNP/ghrelin chimeric peptide. ASB20123 stimulate bone growth. ASB20123 can be used in research of growth disorders and dwarfism .
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Cat. No.: HY-176547
CAS No.: 3069945-78-1
Target:  

FGFR Cytochrome P450

Research Areas:  

Endocrinology

FGFR2/3-IN-3 is a dual-target FGFR2/3 inhibitor with IC50s of 2.7 nM (TEL-FGFR2) and 3.9 nM (TEL-FGFR3), respectively. FGFR2/3-IN-3 has effective activity against both wild-type and mutant FGFR3. FGFR2/3-IN-3 has low CYP3A4 inhibitory effect and hERG toxicity. FGFR2/3-IN-3 improves the imbalance between chondrocyte proliferation and differentiation and promotes bone growth by inhibiting the signaling pathway mediated by mutant FGFR3. FGFR2/3-IN-3 shows a growth-promoting effect in a dwarfism mouse model and has the potential to study bone development disorder-related diseases such as achondroplasia (ACH) .
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Cat. No.: HY-122833
CAS No.: 2833703-74-3
Target:  

FGFR

FGFR3-IN-10 is a selective FGFR3 inhibitor that inhibits FGFR3 kinase activity. FGFR3-IN-10 can be used in research related to cancer, systemic sclerosis, fibrosis, pulmonary fibrosis, achondroplasia, lethal dwarfism, severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN), and Muenke syndrome .
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Cat. No.: HY-P72196
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: ACH; CD 333; CD333; CD333 antigen; CEK 2; CEK2; FGFR 3; FGFR-3; FGFR3; FGFR3_HUMAN; Fibroblast growth factor receptor 3 achondroplasia thanatophoric dwarfism; ; Fibroblast growth factor receptor 3; Heparin binding growth factor receptor; HSFGFR3EX; Hydroxyaryl protein kinase; JTK 4; JTK4; MFR 3; SAM 3; Tyrosine kinase JTK 4; Tyrosine kinase JTK4; Z FGFR 3
Species:  
Source:  
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