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| Product | Description | |
|---|---|---|
| Terfenadine | Nonsedating-type histamine H1-receptor antagonist. Antihistaminic. Group: Biochemicals. Alternative Names: α - [4- (1, 1-Di methyl ethyl) phenyl] -4- (hydroxydiphenyl methyl ) -1-piperidinebutanol; α - (p-tert-Butylphenyl) -4- ( α -hydroxy- α -phenylbenzyl) -1-piperidinebutanol; Allerplus; Cyater; Histadin; MDL 9918; NSC 665802; (±)-Terfenadine. Grades: Highly Purified. CAS No. 50679-08-8. Pack Sizes: 2.5g, 5g, 10g. Molecular Formula: C??H??NO?, Molecular Weight: 471.67. US Biological Life Sciences. |  Worldwide |
| Terfenadine | Terfenadine is a potent open-channel blocker of hERG (IC50=204 nM), formerly used for the treatment of allergic conditions. Uses: Nonsedating-type histamine h1-receptor antagonist. antihistaminic. Synonyms: BRN 5857899; BRN5857899; BRN-5857899; Terfenadine; Seldane; Terfen1-(4-tert-butylphenyl)-4-[4-[hydroxy(diphenyl)methyl]piperidin-1-yl]butan-1-ol. Grades: ≥98%. CAS No. 50679-08-8. Molecular formula: C32H41NO2. Mole weight: 471.67. |  |
| Terfenadine | Terfenadine ((±)-Terfenadine) is a potent open-channel blocker of hERG with an IC 50 of 204 nM [1]. Terfenadine, an H1 histamine receptor antagonist, acts as a potent apoptosis inducer in melanoma cells through modulation of Ca 2+ homeostasis. Terfenadine induces ROS-dependent apoptosis , simultaneously activates Caspase-4, -2, -9 [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (±)-Terfenadine; MDL-991. CAS No. 50679-08-8. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1193. |  |
| Terfenadine EP Impuity C | One impurity of Terfenading, which is a nonsedating-type histamine H1-receptor antagonisst and could be used as as antihistaminic agent. Synonyms: Terfenadine N-Oxide; α-[4-(1,1-Dimethylethyl)phenyl]-4-(hydroxydiphenylmethyl)-1-piperidinebutanol 1-Oxide. Grades: > 95%. CAS No. 634901-83-0. Molecular formula: C32H41NO3. Mole weight: 487.69. | |
| Terfenadine EP Impuity D | One impurity of Terfenading, which is a nonsedating-type histamine H1-receptor antagonisst and could be used as as antihistaminic agent. Grades: > 95%. Molecular formula: C32H39NO. Mole weight: 453.67. | |
| Terfenadine EP Impuity F | One impurity of Terfenading, which is a nonsedating-type histamine H1-receptor antagonisst and could be used as as antihistaminic agent. Grades: > 95%. Molecular formula: C32H37N. Mole weight: 435.66. | |
| 1-Dehydroxy Terfenadine | 1-Dehydroxy Terfenadine. Group: Biochemicals. Alternative Names: 1-[4-[4- (1, 1-Dimethylethyl) phenyl]butyl]-α , α -diphenyl-4-piperidinemethanol; VUF 4591. Grades: Highly Purified. CAS No. 147158-67-6. Pack Sizes: 250mg. Molecular Formula: C32H41NO, Molecular Weight: 455.67. US Biological Life Sciences. | Worldwide |
| Dehydroxydehydro Terfenadine | Dehydroxydehydro Terfenadine. Group: Biochemicals. Alternative Names: 1-[4-[4-(1,1-Dimethylethyl)phenyl]-3-buten-1-yl]-α,α-diphenyl-4-piperidinemethanol. Grades: Highly Purified. Pack Sizes: 100mg. Molecular Formula: C32H39NO, Molecular Weight: 453.66. US Biological Life Sciences. | Worldwide |
| Dehydroxy Terfenadine | Dehydroxy Terfenadine. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 100mg. Molecular Formula: C32H41NO, Molecular Weight: 455.67. US Biological Life Sciences. | Worldwide |
| Fexofenadine (Carboxyterfenadine, Terfenadinecarboxyl ate) | A metabolite of of terfenadine, a H1-Histamine receptor antagonist. Group: Biochemicals. Alternative Names: Carboxyterfenadine, Terfenadinecarboxyl ate. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Fexofenadine-d6 (Carboxyterfenadine-d6, Terfenadinecarboxyl ate) | A metabolite of of terfenadine, a H1-Histamine receptor antagonist. Group: Biochemicals. Alternative Names: Carboxyterfenadine-d6, Terfenadinecarboxyl ate. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Fexofenadine, Hydrochloride (Carboxyterfenadine, Terfenadinecarboxyl ate) | A metabolite of of terfenadine, a H1-Histamine receptor antagonist. Group: Biochemicals. Alternative Names: Carboxyterfenadine, Terfenadinecarboxyl ate. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| R-Fexofenadine (R-Carboxyterfenadine, R-Terfenadinecarboxyl ate) | A metabolite of of terfenadine, a H1-Histamine receptor antagonist. Group: Biochemicals. Alternative Names: R-Carboxyterfenadine, R-Terfenadinecarboxyl ate. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| S-Fexofenadine (S-Carboxyterfenadine, S-Terfenadinecarboxyl ate) | A metabolite of of terfenadine, a H1-Histamine receptor antagonist. Group: Biochemicals. Alternative Names: S-Carboxyterfenadine, S-Terfenadinecarboxyl ate. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| (1-Benzylpiperidin-4-yl)diphenyl-d10-methanol | (1-Benzylpiperidin-4-yl)diphenyl-d10-methanol is an intermediate in the synthesis of Fexofenadine-d10 Hydrochloride, the labeled analogue of Fexofenadine Hydrochloride (F322490), the active metabolite of Terfenadine (T114500), a H1-histamine receptor antagonist. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg, 100mg. Molecular Formula: C25H17D10NO, Molecular Weight: 367.55. US Biological Life Sciences. | Worldwide |
| 1-Oxo Fexofenadine-d10 Methyl Ester | 1-Oxo Fexofenadine-d10 Methyl Ester is the labeled analogue of 1-Oxo Fexofenadine Methyl Ester (O870040), an intermediate in the preparation of Fexofenadine (F322470). It can also be used for the synthesis of an oxidation metabolite of Terfenadine (T114500),a H1-receptor antagonist. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C33H29D10NO4, Molecular Weight: 523.73. US Biological Life Sciences. | Worldwide |
| 2- (4- (4- (4- (Diphenylmethylene) piperidin-1-yl) butanoyl) phenyl) -2-methylpropanoic Acid Methyl Ester | 2- (4- (4- (4- (Diphenylmethylene) piperidin-1-yl) butanoyl) phenyl) -2-methylpropanoic Acid Methyl Ester is an impurity of fexofenadine (F322490), the active metabolite of Terfenadine (T114500), a H1-histamine receptor antagonist. Group: Biochemicals. Grades: Highly Purified. CAS No. 1025909-08-3. Pack Sizes: 100mg, 1g. Molecular Formula: C33H37NO3. US Biological Life Sciences. | Worldwide |
| Azacyclonol | Azacyclonol (γ-pipradol), a metabolite of Terfenadine, is a central depressant agent. Azacyclonol is a ganglion-blocking agent. Azacyclonol can be used to diminish psychoses-induced hallucinations [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: γ-pipradol. CAS No. 115-46-8. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0530. | |
| Decarboxy Fexofenadine (Fexofenadine EP Impurity C) | Decarboxy Fexofenadine is an photodegradation product of Fexofenadine, the active metabolite of Terfenadine, a H1-histamine receptor antagonist. Group: Biochemicals. Alternative Names: 4- (Hydroxydiphenyl methyl ) - α - [4- (1- methyl ethyl) phenyl] -1-piperidinebutanol; Fexofenadine EP Impurity C. Grades: Highly Purified. CAS No. 185066-37-9. Pack Sizes: 5mg. Molecular Formula: C??H??NO?, Molecular Weight: 457.65. US Biological Life Sciences. | Worldwide |
| Fexofenadine | Fexofenadine is Histamine H1 receptor antagonist. It can be used for the treatment of allergy symptoms, such as hay fever, nasal congestion, and urticaria. Uses: Histamine h1 antagonists. Synonyms: Carboxyterfenadine; Terfenadine carboxylate; 4-[1-Hydroxy-4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]butyl]-α,α-dimethyl-benzene-acetic Acid; 4-[4-[4-(Hydroxydiphenylmethyl)-1-piperidinyl]-1-hydroxybutyl]-α,α- dimethylphenylacetic Acid; MDL 16455; MDL16455; MDL-16455; Terfenadine Acid Metabolite. Grades: ≥98%. CAS No. 83799-24-0. Molecular formula: C32H39NO4. Mole weight: 501.66. | |
| Fexofenadine | Fexofenadine (MDL-16455) is an orally active and nonsedative H1 receptor antagonist. Fexofenadine can be used in allergic rhinitis and chronic idiopathic urticarial research [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MDL-16455; Terfenadine carboxylate. CAS No. 83799-24-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0801. | |
| Fexofenadine 1-Methyl Ether Methyl Ester | Fexofenadine 1-Methyl Ether Methyl Ester is an novel intermediate of Fexofenadine (F322470), the active metabolite of Terfenadine (T114500), a H1-histamine receptor antagonist. Group: Biochemicals. Alternative Names: 2- (4- (4- (4- (Hydroxydiphenyl methyl ) piperidin-1-yl) -1-methoxybutyl) phenyl) -2- methyl propanoic Acid Methyl Ester. Grades: Highly Purified. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Fexofenadine hydrochloride | Fexofenadine (MDL-16455) hydrochloride is an orally active and nonsedative H 1 receptor antagonist. Fexofenadine hydrochloride can be used in allergic rhinitis and chronic idiopathic urticarial research [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MDL-16455 hydrochloride; Terfenadine carboxylate hydrochloride. CAS No. 153439-40-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0801A. | |
| (R)-Fexofenadine | (R)-Fexofenadine. Group: Biochemicals. Alternative Names: 4- [ (1R) -1-Hydroxy-4- [4- (hydroxydiphenyl methyl ) -1-piperidinyl] butyl] -a, a-di methyl - Benzene acetic acid; R-Carboxyterfenadine; R-Terfenadinecarboxyl ate. Grades: Highly Purified. CAS No. 139965-10-9. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C32H39NO4. US Biological Life Sciences. | Worldwide |
| (S)-Fexofenadine | (S)-Fexofenadine. Group: Biochemicals. Alternative Names: 4- [ (1S) -1-Hydroxy-4- [4- (hydroxydiphenyl methyl ) -1-piperidinyl] butyl] -a, a-di methyl - Benzene acetic acid; S-Carboxyterfenadine; S-Terfenadinecarboxyl ate. Grades: Highly Purified. CAS No. 139965-11-0. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C32H39NO4. US Biological Life Sciences. | Worldwide |
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