D-Histidine|CAS 351-50-8|DC Chemicals

Cas No.:	351-50-8
Chemical Name:	D-Histidine
Synonyms:	(R)-2-Amino-3-(1H-imidazol-4-yl)propanoic acid;D-Histidine hydrochloride;D-Histidine hydrochloride monohydrate;H-D-His-OH;D-Histidine;HISTIDINE, D-(RG);(D)-histidine;(R)-2-Amino-3-(4-imidazolyl)propionic acid;(R)-2-AMino-3-(4-iMidazolyl)propionic acid;(R)-Histidine;CHEBI:27947;D-2-AMino-4(or 5)iMidazolepropionic acid;D-His-OH;ST069340;D-2-Amino-3-(4-imidazolyl)propionic acid;D-Histidin;D-His;(2R)-2-amino-3-(1H-imidazol-4-yl)propanoic acid;(R)-alpha-Amino-1H-imidazole-4-propionic acid;D-Histamine;(2R)-2-amino-3-(1H-imidazol-5-yl)propanoic acid;PubChem12316;2ez7;D-alpha-Amino-beta-(4-imidazolyl)propionic acid;KSC222G6N;GTPL4679;NIOSH/MS3116000;KS-
SMILES:	O([H])C([C@@]([H])(C([H])([H])C1=C([H])N=C([H])N1[H])N([H])[H])=O
Formula:	C₆H₉N₃O₂
M.Wt:	155.1546
Purity:	>98%
Sotrage:	Powder-20°C3 years4°C2 yearsIn solvent-80°C6 months -20°C1 month

Cat. No.	Product name	Field of application
DC49761	BAY-179	BAY-179 is a potent, selective, and species cross-reactive complex I inhibitor (IC50=79 µM).
DC49760	THP104c	THP104c is a mitochondrial fission inhibitor.
DC42141	D-Histidine	D-Histidine is an enantiomer of L-histidine. L-Histidine is an essential amino acid for infants. L-Histidine is an inhibitor of mitochondrial glutamine transport.
DC40140	Mitochondrial fusion promoter M1	Mitochondrial fusion promoter M1 is a mitochondrial dynamic modulator. Mitochondrial fusion promoter M1 preserves the mitochondrial function and promotes cellular respiration. Mitochondrial fusion promoter M1 alleviates cardiac and brain damage in rats with cardiac ischemia/reperfusion injury.
DC28781	NL-1	NL-1 is a mitoNEET inhibitor with antileukemic effect. NL-1 inhibits REH and REH/Ara-C cells growth with IC50s of 47.35 µM and 56.26 µM, respectively. NL-1-mediated death in leukemic cells requires the activation of the autophagic pathway.
DC76894	ZGL-18	ZGL-18 is an uncoupling protein 1 (UCP1)-inspired mitochondrial uncoupler. ZGL-18 activates brown adipocytes and reduces mitochondrial membrane potential.
DC76893	SHO1122147	SHO1122147 (Compound 7m) affects the mitochondrial electron transport chain, exhibits mitochondrial uncoupling activity (EC50=3.6 μM), and increases the oxygen consumption rate (OCR=69%) and promotes cellular respiration. SHO1122147 is orally active, and can be used in reaearch of obesity and metabolic dysfunction-associated steatohepatitis (MASH).
DC76892	S-15176	S-15176 is an inhibitor of the mitochondrial permeability transition pore (PTP). S-15176 inhibits mitochondrial swelling induced by tert-butylhydroperoxide with an IC50 value of 45.7 μM. S-15176 inhibits PTP opening, prevents mitochondrial membrane potential dissipation and NAD(P)H oxidation, and increases mitochondrial calcium loading capacity. S-15176 is promising for research of ischemia-reperfusion injury.
DC76891	PENAO	PENAO is a potent tumour cell mitochondrial toxin. PENAO inactivates tumor cell mitochondria by targeting inner-membrane adenine nucleotide transferase.
DC76890	LH1513	LH1513 is a dioxalate derivative of l-lysine that inhibits CaOx crystallization with better activity than citrate and pyruvate. LH1513 has potential preventive activity in hyperoxaluria models and effectively prevents urinary CaOx crystal formation in Agxt knockout mice. AGXT-1 is a mitochondrial protein involved in metabolism.