287484-37-1
287484-37-1
Chemical Structure
DL-Histidine-15N
- CAS No.: 287484-37-1
- Formula:C6H9N215NO2
- Molecular Weight:156.15
IUPAC Name: histidine-Na-15N
InChIKey: HNDVDQJCIGZPNO-CDYZYAPPSA-N
SMILES: OC(C([15NH2])CC1=CN=CN1)=O
Biological Activity: DL-Histidine-15N is a 15N-labeled DL-Histidinen (HY-W010209). DL-Histidine is a histidine derivative[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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DL-Histidine-15N | DL-Histidine-15N is a 15N-labeled DL-Histidinen (HY-W010209). DL-Histidine is a histidine derivative. | |||||||||||||||||||||
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DL-Histidine (Standard) | ≥98% | DL-Histidine (Standard) is the analytical standard of DL-Histidine. This product is intended for research and analytical applications. DL-Histidine is a histidine derivative. | ||||||||||||||||||||
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DL-Histidine-13C6,15N3 | DL-Histidine-13C6,15N3 N-Acetyl-S-allyl-L-cysteine | |||||||||||||||||||||
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DL-Histidine-d3 | 99.01% | DL-Histidine-d3 is the deuterium labeled DL-Histidine. | ||||||||||||||||||||
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DL-Histidine | 99.47% | DL-Histidine is a histidine derivative. | ||||||||||||||||||||
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Thiazolylalanine | Thiazolylalanine is a synthetic non-protein amino acid containing a thiazole heterocycle. Thiazolylalanine exhibits dual activities of stimulating protein synthesis and inducing protein degradation in rat reticulocytes, but exerts no effects on protein metabolism or the thermolability of phosphoenolpyruvate carboxykinase in hepatoma cells. Thiazolylalanine can serve as the N-terminal component of tripeptide ligands for the synthesis of various organometallic complexes such as gold, mercury, CyRu (II) Cl2, and Cp*Rh (III) Cl2. Thiazolylalanine finds wide application in the research of breast cancer and other related diseases. | |||||||||||||||||||||
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Histamine-α,α,β,β-d4 dihydrochloride | 98.41% | Histamine-α,α,β,β-d4 (dihydrochloride) is the deuterium labeled Histamine. Histamine is an organic nitrogenous compound involved in local immune responses as well as regulating physiological function in the gut and acting as a neurotransmitter. | ||||||||||||||||||||
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Histamine-d4 | Histamine-d4 (Ergamine-d4) is deuterium labeled Histamine (HY-B1204). Histamine is the agonist for histamine receptor and a vasodilator. Histamine is an organic nitrogen compound that participates in local immune responses, regulates intestinal physiological functions, and acts as a neurotransmitter. Histamine affects p38 MAPK/Akt signaling pathway, exhibits antitumor, antioxidant and anti-inflammatory activities. Histamine can be used in the research of acute myeloid leukemia, malignant melanoma, and renal cell carcinoma. | |||||||||||||||||||||
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L-Tryptophan-d3 | 99.98% | L-Tryptophan-d3 is the deuterium labeled L-Tryptophan. L-Tryptophan (Tryptophan) is an essential amino acid that is the precursor of serotonin, melatonin, and vitamin B3. | ||||||||||||||||||||
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L-Histidine | 99.97% | L-Histidine is an essential amino acid for infants. L-Histidine is an inhibitor of mitochondrial glutamine transport. | ||||||||||||||||||||
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L-Histidine-13C6,15N3 | L-Histidine-13C6,15N3 is 13C and 15N-labeled L-Histidine (HY-N0832). L-Histidine is an essential amino acid for infants. L-Histidine is an inhibitor of mitochondrial glutamine transport. | |||||||||||||||||||||
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L-Hisidine (monohydrocholoride) | 99.76% | L-Hisidine is an essential amino acid for infants. L-Hisidine is an inhibitor of mitochondrial glutamine transport. | ||||||||||||||||||||
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DL-Tryptophan-d3 | 99.64% | DL-Tryptophan-d3 is the deuterium labeled DL-Tryptophan. DL-Tryptophan ((±)-Tryptophan) is an orally effective aryl hydrocarbon receptor (AhR) agonist. DL-Tryptophan reduces the expression of pro-inflammatory cytokines IL-6, TNF-α, IL-1β, as well as liver injury markers aspartate aminotransferase and alanine aminotransferase, and alleviates hepatocyte apoptosis (apoptosis) in sepsis induced by cecal ligation and puncture. DL-Tryptophan can be used in the research of sepsis-related acute liver injury. | ||||||||||||||||||||
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D-Histidine | 99.84% | D-Histidine is an anti-biofilm agent that targets bacterial quorum sensing systems (such as RhlI/RhlR pathway) and has antibacterial activity. D-Histidine works by non-covalently binding to bacterial regulatory factors or copper ion complexes, selectively inhibiting bacterial biofilm formation and motility. D-Histidine downregulates quorum sensing-related gene expression, reduces the synthesis of virulence factors (such as alginate and proteases), and interferes with bacterial membrane stability, inhibiting biofilm formation, promoting the disintegration of mature biofilms, and enhancing antibiotic sensitivity. D-Histidine is also an efficient catalyst for the salt-induced peptide formation (SIPF) reaction, which promotes the condensation of amino acids to form dipeptides (such as dialanine and dilysine) by forming a complex with copper ions (Cu2+). | ||||||||||||||||||||
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L-Histidine-13C6,15N3,d5 hydrochloride hydrate | L-Histidine-13C6,15N3,d5 hydrochloride hydrate is the deuterium, 13C-, and 15-labeled L-Histidine hydrochloride hydrate (HY-W014423). L-Histidine hydrochloride hydrate is an endogenous metabolite. L-Histidine hydrochloride hydrate scavenges hydroxyl radicals and singlet oxygen, regulate the absorption of zinc, copper and iron, exhibits anti-inflammatory and antioxidant activities. L-Histidine hydrochloride hydrate is blood brain barrier penetrable. | |||||||||||||||||||||
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L-Histidine-d5 hydrochloride hydrate | 99.96% | L-Histidine-d5 hydrochloride hydrate is the deuterium labeled L-Histidine hydrochloride hydrate (HY-W014423). L-Histidine hydrochloride hydrate is an endogenous metabolite. L-Histidine hydrochloride hydrate scavenges hydroxyl radicals and singlet oxygen, regulate the absorption of zinc, copper and iron, exhibits anti-inflammatory and antioxidant activities. L-Histidine hydrochloride hydrate is blood brain barrier penetrable. | ||||||||||||||||||||
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3-Methyl-L-histidine-d3 | 99.9% | 3-Methyl-L-histidine-d3 is the deuterium labeled 3-Methyl-L-histidine. 3-Methyl-L-histidine is an endogenous amino acid that can be found in actin and myosin. | ||||||||||||||||||||
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α-FMH | α-FMH (α-Fluoromethylhistidine) is an orally active histidine decarboxylase inhibitor. α-FMH depletes histamine in enterochromaffin-like (ECL) cells, reduces the number and volume density of secretory vesicles in ECL cells, and does not affect histamine storage in mast cells. α-FMH abolishes Omeprazole (HY-B0113)-induced vacuolization of ECL cells and decreases gastrin-induced histamine efflux from ECL cells. α-FMH does not alter the granular characteristics of ECL cells, omeprazole-induced hypertrophy of ECL cells, gastrin-induced pancreastatin-like immunoreactivity efflux, nor does it affect gastric acid secretion induced by histamine or vagal stimulation. α-FMH inhibits basal and gastrin-stimulated gastric acid secretion, reduces acid output induced by gastrin+IBMX (HY-12318), but does not directly affect acid generation in isolated parietal cells. | |||||||||||||||||||||
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D-Histidine monohydrochloride | D-Histidine monohydrochloride is a histidine derivative. | |||||||||||||||||||||
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L-Histidine dihydrochloride | L-Histidine dihydrochloride is a histidine derivative. | |||||||||||||||||||||
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4-Methyl-imidazole-d3 | 97% | 4-Methyl-imidazole-d3 is the deuterium labeled 4-Methyl-imidazole. | ||||||||||||||||||||
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