24-Diamino-6-hydroxypyrimidine
CAS No. 56-06-4
24-Diamino-6-hydroxypyrimidine( DAHP )
Catalog No. M20881 CAS No. 56-06-4
24-Diamino-6-hydroxypyrimidine (DAHP) is a selective specific inhibitor of GTP cyclohydrolase I the rate limiting step for de novo pterin synthesis.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 43 | In Stock |
|
| 100MG | 37 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product Name24-Diamino-6-hydroxypyrimidine
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NoteResearch use only, not for human use.
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Brief Description24-Diamino-6-hydroxypyrimidine (DAHP) is a selective specific inhibitor of GTP cyclohydrolase I the rate limiting step for de novo pterin synthesis.
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Description24-Diamino-6-hydroxypyrimidine (DAHP) is a selective specific inhibitor of GTP cyclohydrolase I the rate limiting step for de novo pterin synthesis.
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In Vitro——
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In Vivo——
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SynonymsDAHP
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PathwayOthers
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TargetOther Targets
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RecptorGTP cyclohydrolase I
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Research Area——
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Indication——
Chemical Information
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CAS Number56-06-4
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Formula Weight126.12
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Molecular FormulaC4H6N4O
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Purity>98% (HPLC)
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SolubilityDMSO:25 mg/mL (198.22 mM)
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SMILESNc1cc(=O)[nH]c(N)n1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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α-Casein (90-95)
α-Casein (90-95)
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Secretin Acetate, po...
Secretin (swine), a neuroendocrine hormone, is the first hormone to be identifie and is secreted by S cells that are localized primarily in the mucosa of the duodenum. Secretin also is a 27-amino acid peptide, which acts on secretin receptors. Secretin is expressed by cells in all mature enteroendocrine cell subsets and can be prompted by fatty acids. Secretin stimulates the secretion of pancreatic water and bicarbonate. Secretin exerts various effects in organs, can be used for the research of digestive system, central nervous system and energy metabolism.
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MRGPRX4 modulator-2
MRGPRX4 modulator-2 (compound 1-55) is a highly potent antagonist of MRGPRX4 with an IC50 value of less than 100 nM.
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