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| Product | Description | |
|---|---|---|
| Desipramine hydrochloride | Desipramine hydrochloride. Group: Biochemicals. Alternative Names: 10,11-Dihydro-N-methyl-5H-dibenz[b,f]azepine-5-propanamine; G-35020; JB-8181. Grades: Highly Purified. CAS No. 58-28-6. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. Molecular Formula: C18H23ClN2, Molecular Weight: 302.84. US Biological Life Sciences. |  Worldwide |
| Desipramine hydrochloride | Desipramine hydrochloride is an inhibitor of norepinephrine transporter ( NET ), 5-HT transporter ( SERT ) and dopamine transporter ( DAT ) with K i s of 4, 61 and 78,720 nM, respectively. Uses: Scientific research. Group: Signaling pathways. CAS No. 58-28-6. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B1272. |  |
| 2-Hydroxy Desipramine-d6 Hydrochloride | 2-Hydroxy Desipramine-d6 Hydrochloride is a labeled salt analogue of 2-Hydroxy Desipramine (H936500), a metabolite of Desipramine Hydrochloride (D290050), a tricyclic antidepressant that is a more potent inhibitor of the norepinephrine transporter than the serotonin transporter. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug, 5mg. Molecular Formula: C18H17D6ClN2O, Molecular Weight: 324.88. US Biological Life Sciences. | Worldwide |
| 2-Hydroxydesipramine Dihydrochloride | 2-Hydroxydesipramine Dihydrochloride is a metabolite of Desipramine, a tricyclic antidepressant that is a more potent inhibitor of the norepinephrine transporter than the serotonin transporter. Synonyms: 5H-Dibenz(b,f)azepin-2-ol, 10,11-dihydro-5-(3-(methylamino)propyl)-, hydrochloride (1:2); 5-[3-(Methylamino)propyl]-10,11-dihydro-5H-dibenzo[b,f]azepin-2-ol hydrochloride (1:2); 2-Hydroxydesmethylimipramine dihydrochloride; 10,11-Dihydro-5-[3-(methylamino)propyl]-5H-dibenz[b,f]azepin-2-ol dihydrochloride. Molecular formula: C18H24Cl2N2O. Mole weight: 355.30. |  |
| Desipramine-2,4,6,8-d4 Hydrochloride (10,11-Dihydro-N-methyl-5H-dibenz[b,f]azepine-5-propanamine-d4, G-35020-d4, JB-8181-d4, NSc-114901-d4, Norpramin-d4, Nortimil-d4, Pertofran-d4, Pertofrane-d4, Petylyl-d4) | Desipramine is an active metabolite of imipramine and has been found to be useful in the treatment of neuropathic pain. It may also be used to treat symptoms of cocaine withdrawal. Desipramine is a tricyclic antidepressant (TCA). Tricyclic antidepressants contain a characteristic three ringed nucleus structure. They act primarily as serotoninnorepinephri ne reuptake inhibitors. Tricyclic antidepressants are mainly used as antidepressants, but have also been for the treatment of anxiety disorders and attention hyperactivity disorder and as an adjunct to certain analgesics to treat chronic pain. In many treatments they have been replaced by other compounds with fewer sideeffects. Group: Biochemicals. Alternative Names: 10,11-Dihydro-N-methyl-5H-dibenz[b,f]azepine-5-propanamine-d4; G-35020-d4; JB-8181-d4; NSc-114901-d4; Norpramin-d4; Nortimil-d4; Pertofran-d4; Pertofrane-d4; Petylyl-d4. Grades: Highly Purified. CAS No. 61361-34-0. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Desipramine Ethyl Carbamate | Desipramine Ethyl Carbamate is derived from 3-Dimethylaminopropyl Chloride Hydrochloride (D461800), which is is used mainly as a pharmaceutical intermediate for the synthesis of many types of drugs, as an agricultural chemical intermediate, as a photographic chemical intermediate, and as a biochemical reagent for enzyme and other studies. The compound shows mutagenic activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 27097-69-4. Pack Sizes: 50mg, 100mg. Molecular Formula: C21H26N2O2, Molecular Weight: 338.44. US Biological Life Sciences. | Worldwide |
| Proadifen hydrochloride | Proadifen (SKF-525A) hydrochloride is a non-competitive Cytochrome P450 inhibitor with an IC 50 value of 19 μM. Proadifen hydrochloride reduces monoamine oxidase A ( MAO-A ) activity and reverses the antidepressantlike behavioral effect of Imipramine (HY-B1490A) and Desipramine (HY-B1272A) in rats. Proadifen hydrochloride also reduces N, N-dimethyltryptamine ( DMT ) metabolism in liver microsomes and inhibits N-demethylationand Acridone (HY-W007771) formation. Proadifen hydrochloride augments Lipopolysaccharide (LPS) (HY-D1056)-induced fever and exacerbates Prostaglandin E2 (PGE2) (HY-101952) levels in the rat. Proadifen hydrochloride is promising for research of metabolism-related deseases, ovarian carcinoma, inflammation and dopamine neurons-related deseases [1] [2] [3] [4] [5] [6]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SKF-525A; U-5446; RP-5171. CAS No. 62-68-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg; 500 mg. Product ID: HY-B1311. | |
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