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replacement

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    TargetMol | Inhibitors_Agonists
Deoxycorticosterone acetate
DOC acetate, Cortexone acetate, 11-Deoxycorticosterone acetate
T303356-47-3
Deoxycorticosterone acetate (Cortexone acetate) is the 21-acetate derivative of desoxycorticosterone, used for intramuscular injection for replacement therapy of the adrenocortical steroid.
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Testosterone phenylpropionate
Testosterone hydrocinnamate, Testosterone 17-phenylpropionate, Retandrol
T31301255-49-8
Testosterone phenylpropionate (Testosterone 17-phenylpropionate)is a steroid indicated for testosterone replacement therapy in sterilization, missing testicle, hypopituitarism, and osteoporosis.
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Glycocyamine
Guanidoacetic acid, 2-Guanidinoacetic acid
T4238352-97-6
Glycocyamine (2-Guanidinoacetic acid), a precursor of creatine, is a replacement of dietary arginine and could support overall energy homeostasis of the bird. Glycocyamine is an important marker for renal failure, kidney transplantation, and the renal metabolic activity. The compound is a metabolite of guanidine.
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H-D-cis-Hyp-OH
D-allo-Hydroxyproline, cis-4-Hydroxy-D-proline
T47122584-71-6
H-D-cis-Hyp-OH (D-allo-Hydroxyproline) belongs to the class of organic compounds known as proline and derivatives. Proline and derivatives are compounds containing proline or a derivative thereof resulting from a reaction of proline at the amino group or the carboxyl group, or from the replacement of any hydrogen of glycine by a heteroatom.
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TargetMol | Inhibitor Sale
N-Acetyl-L-leucine
T47981188-21-2
N-Acetylleucine belongs to the class of organic compounds known as leucine and derivatives. Leucine and derivatives are compounds containing leucine or a derivative thereof resulting from reaction of leucine at the amino group or the carboxy group, or fro
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alpha-D-glucose
α-D-Glucose, alpha-Glucose, α-Dextrose
T4884492-62-6
alpha-D-glucose (α-Dextrose) is a primary source of energy for living organisms. It is naturally occurring and is found in fruits and other parts of plants in its free state. It is used therapeutically in fluid and nutrient replacement.
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Desmopressin acetate trihydrate
Vasopressin 1-Desamino-8-arginine, Desmogalen, Deamino Arginine Vasopressin, Adiuretin
T2129662357-86-2
Desmopressin acetate is a synthetic replacement for vasopressin, which reduces urine production. Medical use of Desmopressin acetate includes: (a) bed wetting; (b) diabetes insipidus; (c) nighttime urination; (d) clotting disorders.
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2'-Deoxyadenosine monohydrate
T275216373-93-6
Deoxyadenosine, a deoxyribonucleoside, is a derivative of the nucleoside adenosine, differing from the latter by the replacement of a hydroxyl group (-OH) by hydrogen (-H) at the 2' position of its ribose sugar moiety.
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Lyso-Globotriaosylceramide (d18:1)
Lyso-Globotriaosylceramide (d18:1)
T37291126550-86-5
Lyso-globotriaosylceramide is a form of globotriaosylceramide that is lacking the fatty acyl group. It binds to Shiga toxin 1 (Stx1) in the presence of cholesterol and phosphatidylcholine but does not bind Stx2. It also reduces viability and aggregation of human neutrophils induced by phorbol 12-myristate 13-acetate when used at concentrations of 50 and 1 μM, respectively. Lyso-globotriaosylceramide accumulates in the brain, heart, kidney, liver, lung, and spleen in a mouse model of Fabry disease, a lysosomal storage disorder characterized by a deficiency in the enzyme α-galactosidase A. It also accumulates in the urine, kidney, and plasma of patients with Fabry disease. Lyso-globotriaosylceramide levels decrease in response to administration of the α-galactosidase inhibitor 1-deoxygalactonojirimycin in a transgenic mouse model of Fabry disease. Decreases in plasma and urine concentrations of lyso-globotriaosylceramide have been used as a biomarker for efficacy of enzyme replacement therapy (ERT) and other therapies in the treatment of Fabry disease.
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Spinacine
T3729859981-63-4
Spinacine has been isolated from spinach and the roots of Panax ginseng. This conformationally constrained amino acid is a structural element in certain biologically active compounds as glucagon antagonists and angiotensin II receptor antagonists. Spinacine can be inserted as a His replacement with a locked imidazole moiety for elucidating the role of the lateral heterocycle in the activity of a peptide.
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3-Methyl-L-histidine
T8274368-16-1
3-Methylhistidine belongs to the class of organic compounds known as histidine and derivatives. Histidine and derivatives are compounds containing cysteine or a derivative thereof resulting from reaction of cysteine at the amino group or the carboxy group
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