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| Product | Description | |
|---|---|---|
| Freeze-dried powder bottle for medicine | This packaging material has a variety of colors to choose from, the use of electroplating/spraying/screen printing/hot stamping process, making the bottle appearance more beautiful. Product ID: PM-073. Category: Double cavity mixed one bottle. Product Keywords: Cosmetic Plastic Packaging; Freeze-dried powder bottle for medicine; PM-073; Double cavity mixed one bottle;. Administration route: Total height: 116mm. Straight diameter: 33mm. Pump output: 0.23CC. Cover material: AS/PCTG. Pump head material: PP. Bottle material: AS/PCTG. |  |
| Freeze dried snow film | Freeze dried snow film. Product ID: CDC10-0701. Category: Cosmetic Packaging Material. Product Keywords: Cosmetic Ingredients; Mask; CDC10-0701; Freeze dried snow film; Cosmetic Packaging Material;. | |
| Freeze-dried Tencel Mask | Freeze-dried Tencel Mask. Product ID: CDC10-0700. Category: Cosmetic Packaging Material. Product Keywords: Cosmetic Ingredients; Mask; CDC10-0700; Freeze-dried Tencel Mask; Cosmetic Packaging Material;. | |
| Fremanezumab | Fremanezumab is a humanized monoclonal antibody targeting calcitonin gene-related peptide (CGRP). Fremanezumab has been investigated for the prevention of high-frequency episodic and chronic migraine. Synonyms: TEV-48125. CAS No. 1655501-53-3. |  |
| Fremanezumab | Fremanezumab (TEV-48125) is a humanized lgG2 monoclonal antibody that selectively and potently binds to calcitonin gene related peptide (CGRp) (IC50 values = 7.943 nM). Fremanezumab binds to mouse CGRP with an IC50 value of 19.6 nM. Fremanezumab counteracts anti-inflammatory effects of CGRP in vitro, including CGRP-mediated inhibition of LPS (HY-D1056)-induced microglial activation. Fremanezumab selectively inhibits the activation of Aδ meningeal nociceptors by cortical spreading depression (CSD) in rats. Fremanezumab can be used for the study of inflammation and chronic migraine[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: TEV-48125; LBR-101; PF-04427429; RN-307. CAS No. 1655501-53-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99019. |  |
| Frenatin-1 | Frenatin-1 is an antimicrobial peptide with selective activity. Frenatin-1 is only active against Micrococcus luteus (MIC=25 μg/ml) and not against Bacillus cereus, Escherichia coli, Leuconostoc mesenteroides, Micrococcus luteus, Pastewella haemolytica, Staphylococcus aureus, Streptococcus faecalis and Streptococcus uberis. | |
| Frenatin-2 | Frenatin-2 is an antimicrobial peptide with selective activity. Frenatin-2 is only active against Micrococcus luteus (MIMC=50 μg/ml) and not against Bacillus cereus, Escherichia coli, Leuconostoc mesenteroides, Micrococcus luteus, Pastewella haemolytica, Staphylococcus aureus, Streptococcus faecalis and Streptococcus uberis. | |
| Frenatin 3 | Frenatin 3 inhibits the production of nitric oxide by the enzyme neuronal nitric oxide synthase at a micromolar concentration by binding to its regulatory protein, Ca2+ calmodulin, a protein known to recognize and bind amphipathic alpha-helices. Grade: >95% by HPLC. Molecular formula: C88H146N24O24S. Mole weight: 1956.31. | |
| Frenatin-3 | The peptide frenatin 3 is a major component of the skin secretion of the Australian giant tree frog, Litoria infrafrenata. | |
| Frenatin-4 | Frenatin-4 is a very weak antimicrobial peptide since it does not show activity below 100 μg/ml against Bacillus cereus, Escherichia coli, Leuconostoc mesenteroides, Micrococcus luteus, Pastewella haemolytica, Staphylococcus aureus, Streptococcus faecalis and Streptococcus uberis. | |
| Frenlosirsen | Frenlosirsen is an antisense oligonucleotide targeted to IRF4. It is used for study of relapsed/refractory multiple myeloma (RRMM). Uses: Scientific research. Category: Signaling pathways. Alternative Names: ION-935918; ION251. CAS No. 2304711-81-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-177632. | |
| Frenlosirsen | Frenlosirsen is an interferon regulatory factor 4 (IRF4) synthesis reducer, with antineoplastic properties. Synonyms: all-P-ambo-2'-O,4'-C-[(1S)-ethane-1,1-diyl]-P-thioadenylyl-(3'→5')-2'-O,4'-C-[(1S)-ethane-1,1-diyl]-P-thioguanylyl-(3'→5')-P-thiothymidylyl-(3'→5')-P-thiothymidylyl-(3'→5')-2'-deoxy-P-thioguanylyl-(3'→5')-P-thiothymidylyl-(3'→5')-2'-deoxy-P-thioadenylyl-(3'→5')-2'-deoxy-P-thioadenylyl-(3'→5')-2'-deoxy-P-thioadenylyl-(3'→5')-P-thiothymidylyl-(3'→5')-2'-deoxy-P-thioguanylyl-(3'→5')-2'-O-(2-methoxyethyl)-P-thioadenylyl-(3'→5')-2'-O-(2-methoxyethyl)-P-thioguanylyl-(3'→5')-2'-O-(2-methoxyethyl)-5-methyl-P-thiouridylyl-(3'→5')-2'-O,4'-C-[(1S)-ethane-1,1-diyl]-5-methyl-P-thiocytidylyl-(3'→5')-2'-O,4'-C-[(1S)-ethane-1,1-diyl]guanosine; DNA, d(P-thio)((2',5'-anhydro-6'-deoxy-4'-C-(hydroxymethyl)-alpha-L-mannofurano)A-(3'->4')-(2',5'-anhydro-6'-deoxy-4'-C-(hydroxymethyl)-alpha-L-mannofurano)G-T-T-G-T-A-A-A-T-G-(2'-O-(2-methoxyethyl))rA-(2'-O-(2-methoxyethyl))rG-(2'-O-(2-methoxyethyl))m5rU-(3'->4')-(2',5'-anhydro-6'-deoxy-4'-C-(hydroxymethyl)-alpha-L-mannofurano)m5C-(3'->4')-(2',5'-anhydro-6'-deoxy-4'-C-(hydroxymethyl)-alpha-L-mannofurano)G). CAS No. 2304711-81-5. Molecular formula: C177H226N63O89P15S15. Mole weight: 5605.71. | |
| Frenlosirsen sodium | Frenlosirsen sodium is an antisense oligonucleotide targeted to IRF4. It is used for study of relapsed/refractory multiple myeloma (RRMM). Uses: Scientific research. Category: Signaling pathways. Alternative Names: ION-935918 sodium; ION251 sodium. CAS No. 2304711-82-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-177632A. | |
| Frenolicin | Frenolicin is produced by the strain of Streptomyces fradiae. It has anti-gram-positive bacterial and fungal (weak) activity. Synonyms: Frenolicine; (1R,3S,4aS,10aR)-3,4,5,10-Tetrahydro-9-hydroxy-5,10-dioxo-1-propyl-4a,10a-epoxy-1H-naphtho(2,3-C)pyran-3-acetic acid. CAS No. 10023-07-1. Molecular formula: C18H18O7. Mole weight: 346.33. | |
| Frenolicin B | One of the antibiotics produced by the strain of Streptomyces roseofulvus AM-3876. It has antifungal and mycoplasma activities. Synonyms: (3aR,5R,11bR)-7-hydroxy-5-propyl-3,3a,5,11b-tetrahydro-2H-furo[3,2-b]naphtho[2,3-d]pyran-2,6,11-trione; (1R)-1β-Propyl-3,4,5,10-tetrahydro-4α,9-dihydroxy-5,10-dioxo-1H-naphtho[2,3-c]pyran-3α-acetic acid 3,4-lactone. CAS No. 68930-68-7. Molecular formula: C18H16O6. Mole weight: 328.32. | |
| Frentizole | Frentizole is a novel inhibitor of the Aβ-ABAD interaction (IC50 = 200 lM). Frentizole, a nontoxic antiviral and immunosuppressive agent used clinically in rheumatoid arthritis and systemic lupus erythematosus, displayed a slightly improved activity (IC50 = 200 lM) compared to thioflavine T (IC50 = 230 lM). Uses: Anti-alzheimer agents; amyloid-β inhibitor. Synonyms: LY 53616; LY53616; LY-53616; Frentizole; 1-(6-methoxy-1,3-benzothiazol-2-yl)-3-phenylurea; 7EY946394I; frentizole; mono-hydrate of frentizole; FRENTIZOLE; 26130-02-9; Frentizol; Compound 53616; MLS000555007; CHEMBL128988; UNII-7EY946394I; 1-(6-methoxy-1,3-benzothiazol-2-yl)-3-phenylurea; NCGC00160657-01; SMR000147124; 1-(6-Methoxy-benzothiazol-2-yl)-3-phenyl-urea; DSSTox_CID_26279; DSSTox_RID_8150. CAS No. 26130-02-9. Molecular formula: C15H13N3O2S. Mole weight: 299.35. | |
| Frequentin | Produced by the strain of Penicillum frequentans and Pen. palitans, Frequentin has the activity of resisting ear mold, mucor mold, ploughshare mold and aspergillus. Synonyms: Frequentine; 6-[(1E,3E)-hepta-1,3-dienyl]-3,4-dihydroxy-2-oxocyclohexane-1-carbaldehyde; 6-hepta-1,3-dienyl-3,4-dihydroxy-2-oxocyclohexane-1-carbaldehyde. Grade: >98%. CAS No. 29119-03-7. Molecular formula: C14H20O4. Mole weight: 252.31. | |
| Frescile | Frescile. CAS No. 85351-07-1. VIGON Item # 503219. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers, orange nitrile. |  America & Internationally |
| Freselestat | Freselestat is a high affinity and selective human neutrophil elastase 1 (HNE1) inhibitor (Ki = 12 nM) with >100-fold less activity at other related proteases including trypsin, pancreatic elastase, collagenase and murine macrophage elastase. Freselestat can be used as treatment for neutrophil-predominant inflammatory lung diseases. Synonyms: 2-(5-amino-6-oxo-2-phenylpyrimidin-1-yl)-N-[1-(5-tert-butyl-1,3,4-oxadiazol-2-yl)-3-methyl-1-oxobutan-2-yl]acetamide; ONO6818; ONO 6818; ONO-6818. Grade: 95%. CAS No. 208848-19-5. Molecular formula: C23H28N6O4. Mole weight: 452.51. | |
| Fresh Ginger Oil | Ginger is a knotted, thick, beige, underground stem also known as rhizome The stem extends roughly 12 inches above ground with long, narrow, ribbed green leaves coupled with white or yellowish-green flowers Ginger has a slightly biting and hot note. it's aroma is rich, sweet, warm and has a distinctive woody olfactory note. Uses: Essential Oils, Flavor, Cosmetic and Care. Group: Plant Extracts. INCI Names: Zingiber Officinale (Ginger) Root Oil. Grades: FOOD GRADE. CAS No. 8007-08-7; 84696-15-1. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: FG-001. Olfactive Profile: Warm, spicy, pungent, peppered, woody, earthy, sweet, citrus/lemony odour. EC No: 283-634-2. FEMA No: 2522. Origin: Indonesia. |  New Jersey |
| Freskomenthe ® | Freskomenthe ® (2-Secondary Butyl Cyclohexanone). CAS No. 14765-30-1. FEMA No. 3261. Kosher: Y. VIGON Item # 500891. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| Fresolimumab | Fresolimumab (GC1008) is a human monoclonal antibody against TGF-β that neutralizes all mammalian active subtypes of TGF-β. The binding affinity of Fresolimumab to TGF-β2 is 1.8 nM. Fresolimumab improves Bleomycin (HY-108345)-induced acute lung injury. Fresolimumab radiolabeled with 89Zr can be used for PET analysis of TGF-β expression, antibody uptake and organ distribution. Fresolimumab can be used in the study of cancer, osteogenesis imperfecta, fibrosis and kidney disease[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: GC1008. CAS No. 948564-73-6. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-P99020. | |
| Fresolimumab | Fresolimumab is a human monoclonal antibody targeting transforming growth factor beta (TGF-β). Fresolimumab inhibits the activity of TGF-beta, which may result in the suppression of tumor cell growth, angiogenesis, and migration. Synonyms: GC1008; GC 1008; GC-1008. CAS No. 948564-73-6. | |
| FRETS-VWF73 | FRETS-VWF73 is a synthetic 73-amino-acid peptide that can be used as a fluorogenic substrate for ADAMTS13 assay. Synonyms: H-Asp-Arg-Glu-{Dap(Nma)}-Ala-Pro-Asn-Leu-Val-Tyr-Met-Val-Thr-Gly-{Dap(Dnp)}-Pro-Ala-Ser-Asp-Glu-Ile-Lys-Arg-Leu-Pro-Gly-Asp-Ile-Gln-Val-Val-Pro-Ile-Gly-Val-Gly-Pro-Asn-Ala-Asn-Val-Gln-Glu-Leu-Glu-Arg-Ile-Gly-Trp-Pro-Asn-Ala-Pro-Ile-Leu-Ile-Gln-Asp-Phe-Glu-Thr-Leu-Pro-Arg-Glu-Ala-Pro-Asp-Leu-Val-Leu-Gln-Arg-OH. Molecular formula: C370H583N103O113S. Mole weight: 8314.28. | |
| Frexalimab | Frexalimab (SAR441344) is a second-generation monoclonal antibody targeting the CD40 ligand (CD40L) with a good safety profile. Frexalimab inhibits the binding between CD40 and CD40L to modulate immune response. Frexalimab is likely to help prevent the process of β-cell destruction. Frexalimab is proming for multiple sclerosis, lupus erythematosus, Sj grens syndrome and type I diabetes research[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: SAR441344; INX-021. CAS No. 2515463-86-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99625. | |
| FRG8701 | FRG-8701 is a novel Histamine H2 receptor antagonist (IC50= 0.25~ 0.43 μM). FRG-8701 has relatively long-lasting antisecretory ef fects in comparison with famotidine and cimetidine. Synonyms: FRG8701; FRG 8701; FRG-8701; 2-(furan-2-ylmethylsulfinyl)-N-[3-[3-(piperidin-1-ylmethyl)phenoxy]propyl]acetamide; FRG 8701; FRG-8701; N-(3-(3-(piperidinylmethyl)phenoxy)propyl)-2-(furfurylsulfinyl)acetamide. CAS No. 108498-50-6. Molecular formula: C22H30N2O4S. Mole weight: 418.55. | |
| Friedelanol | Friedelanol is a triterpenoids isolated from the herbs of Celastrus stylosus Wall. It can rearrange to the isomer, ursolic acid, or be oxidized to taraxasterol and amyrin. Synonyms: Friedelan-3-ol; epi-Friedelinol; Friedelan-3alpha-ol. Grade: 98%. CAS No. 5085-72-3. Molecular formula: C30H52O. Mole weight: 428.75. | |
| Friedelin | Friedelin is derived from the leaves of Maytenus ilicifolia (Mart). Friedelin is an orally active non-competitive inhibitor of CYP3A4, with IC50 and Ki values of 10.79 μM and 6.16 μM, respectively. Friedelin is also a competitive inhibitor of CYP2E1, with IC50 and Ki values of 22.54 μM and 18.02 μM, respectively. Friedelin can be used in research related to inflammation, neurological diseases, and metabolic disorders[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 559-74-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N4110. | |
| Friedelin | Friedelin. CAS No. 559-74-0. Cenik is your partner of choice for specialised chemicals. We don't just provide products - we supply solutions to your technical and regulatory specifications. |  |
| Friedelin | Botanical Source: Group: Biochemicals. Alternative Names: 3-Friedelanone. Grades: Plant Grade. CAS No. 559-74-0. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| friedelin synthase | The enzyme from Kalanchoe daigremontiana also gives traces of other triterpenoids. Group: Enzymes. Enzyme Commission Number: EC 5.4.99.50. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5593; friedelin synthase; EC 5.4.99.50. Cat No: EXWM-5593. |  |
| Fringe Tree Bark Powder | Fringe Tree Bark Powder. |  CA, FL & NJ |
| FriO I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 20-fold overdigestion with enzyme more than 90% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 1000U; 5000U. GRGCY↑C C↓YCGRG. Activity: 20000u.a./ml. Appearance: 10 X SE-buffer Y, BSA. Storage: -20°C. Form: Liquid. Source: Flavobacterium rigense O. Pack: 10 mM Tris-HCl (pH 7.5); 200 mM KCl; 0.1 mM EDTA; 200 μg/ml BSA; 7 mM 2-mercaptoethanol; 50% glycerol. Cat No: ET-1113RE. | |
| Friulimicin A | An antibiotic originally isolated from Actinoplanes friuliensis sp. HAG 010964. Friulimicin A has the activity of inhibiting the synthesis of peptidoglycan. It is a naturally occurring cyclic lipopeptide, with excellent activity against gram-positive pathogens through cell wall interruption, including multidrug-resistant strains. Molecular formula: C58H92N14O19. Mole weight: 1289.43. | |
| Friulimicin B | An antibiotic originally isolated from Actinoplanes friuliensis sp. HAG 010964. Friulimicin B has the activity of inhibiting the synthesis of peptidoglycan. It is a naturally occurring cyclic lipopeptide, with excellent activity against gram-positive pathogens through cell wall interruption, including multidrug-resistant strains. Synonyms: Friulimycin B; 2,2'-((6S,9R,15S,21S,24S,26aR,33S,34S,36aS)-33-((S)-4-amino-2-((Z)-12-methyltridec-3-enamido)-4-oxobutanamido)-9-((R)-1-aminoethyl)-24-((S)-1-carboxyethyl)-6-isopropyl-34-methyl-5,8,11,14,17,20,23,26,32,36-decaoxotetratriacontahydro-1H,5H-pyrido[1,2-a]pyrrolo[1,2-y][1,4,7,10,13,16,19,22,25,28]decaazacyclohentriacontine-15,21-diyl)diacetic acid. Grade: >98%. CAS No. 239802-15-4. Molecular formula: C59H94N14O19. Mole weight: 1303.48. | |
| FRM-024 | FRM-024 is a central nervous system-penetrant, orally active γ-secretase modulator and Aβ42 lowering agent. FRM-024 is used for the research of familial Alzheimer's disease[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2085780-87-4. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-115726. | |
| Fromyl-L-Valine | An intermediate of gramicidin A biosynthesis. Synonyms: For-L-Val-OH; N-Formyl-L-valine; FOR-VAL-OH; N-Formyl-valin; 2-formamido-3-methyl-butanoic acid; FORMYL-L-VALINE. Grade: ≥ 98% (HPLC). CAS No. 4289-97-8. Molecular formula: C6H11NO3. Mole weight: 145.16. | |
| Fromyl-L-Valine | Fromyl-L-Valine. Group: Biochemicals. Alternative Names: For-L-Val-OH. Grades: Highly Purified. CAS No. 4289-97-8. Pack Sizes: 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| Fromyl-L-Valine 98+% (HPLC) | Fromyl-L-Valine 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Frost Resistance Benzene-Soluble Polyamide Resin | This product is a frost resistance polyamide resin with low molecular weight has excellent properties and inter-solubility with nitrocellulose. When these resins are used with pigment additives, the final product will display bright colors and gloss. |  |
| Frovatriptan | Frovatriptan. Uses: For analytical and research use. Alternative Names: 3-(methylamino)-2,3,4,9-tetrahydro-1H-carbazole-6-carboxamide. CAS No. 147009-08-3. Molecular formula: C14H17N3O2S. Mole weight: 243.30. Catalog: APB147009083. |  |
| Frovatriptan-d3 Succinate | One of the isotopic labelled salt of Frovatriptan, which has been found to be a serotonin 5-HT1B/1D receptor agonist. Synonyms: (3R)-2,3,4,9-Tetrahydro-3-(methylamino)-1H-carbazole-6-carboxamide Butanedioic Acid-d3. Molecular formula: C14H14N3OD3.C4H6O4. Mole weight: 364.42. | |
| Frovatriptan Impurity 1 | Frovatriptan Impurity 1. Uses: For analytical and research use. Alternative Names: 3-(methylamino)-2,3,4,9-tetrahydro-1H-carbazole-5-carboxamide. Molecular formula: C14H17N3O. Mole weight: 243.3. Catalog: APB05978. | |
| Frovatriptan Impurity 1 | Frovatriptan Impurity 1. Grade: > 95%. Molecular formula: C14H17N3O. Mole weight: 243.31. | |
| Frovatriptan Impurity 10 | Frovatriptan Impurity 10. Uses: For analytical and research use. Molecular formula: C14H17N3O. Mole weight: 243.31. Catalog: APB10493. | |
| Frovatriptan Impurity 11 | Frovatriptan Impurity 11. Grade: > 95%. Molecular formula: C14H15N3O2. Mole weight: 257.29. | |
| Frovatriptan Impurity 11 | Frovatriptan Impurity 11. Uses: For analytical and research use. CAS No. 214917-60-9. Molecular formula: C17H21N3O5. Mole weight: 347.37. Catalog: APB214917609. | |
| Frovatriptan Impurity 12 | Frovatriptan Impurity 12. Grade: > 95%. Molecular formula: C14H17N3O2. Mole weight: 259.31. | |
| Frovatriptan Impurity 2 | Frovatriptan Impurity 2. Uses: For analytical and research use. Alternative Names: 3-(methylamino)-2,3,4,9-tetrahydro-1H-carbazole-7-carboxamide. Molecular formula: C14H17N3O. Mole weight: 243.3. Catalog: APB05979. | |
| Frovatriptan Impurity 2 | Frovatriptan Impurity 2. Grade: > 95%. Molecular formula: C7H9N3O. Mole weight: 151.17. | |
| Frovatriptan Impurity 3 | Frovatriptan Impurity 3. Uses: For analytical and research use. Molecular formula: C16H28O4. Mole weight: 284.4. Catalog: APB10487. | |
| Frovatriptan Impurity 3 | Frovatriptan Impurity 3. Uses: For analytical and research use. Alternative Names: 3-hydrazinylbenzamide. CAS No. 473927-51-4. Molecular formula: C7H9N3O. Mole weight: 151.17. Catalog: APB473927514. | |
| Frovatriptan Impurity 3 | Frovatriptan Impurity 3. Grade: > 95%. Molecular formula: C14H17N3O. Mole weight: 243.31. | |
| Frovatriptan Impurity 4 | Frovatriptan Impurity 4. Grade: > 95%. Molecular formula: C14H17N3O. Mole weight: 243.31. | |
| Frovatriptan Impurity 4 | Frovatriptan Impurity 4. Uses: For analytical and research use. CAS No. 107431-14-1. Molecular formula: C13H25NO2. Mole weight: 227.35. Catalog: APB107431141. | |
| Frovatriptan Impurity 5 | Frovatriptan Impurity 5. Uses: For analytical and research use. Molecular formula: C14H16N2O2. Mole weight: 244.29. Catalog: APB10489. | |
| Frovatriptan Impurity 5 | Frovatriptan Impurity 5. Synonyms: 3-Hydrazinobenzamide; Benzamide, 3-hydrazino-; 3-Carboxamidophenyl hydrazine. Grade: > 95%. CAS No. 473927-51-4. Molecular formula: C7H9N3O. Mole weight: 151.17. | |
| Frovatriptan Impurity 6 | Frovatriptan Impurity 6. Grade: > 95%. Molecular formula: C16H28O4. Mole weight: 284.40. | |
| Frovatriptan Impurity 6 | Frovatriptan Impurity 6. Uses: For analytical and research use. Molecular formula: C14H15N3O2. Mole weight: 257.29. Catalog: APB10488. | |
| Frovatriptan Impurity 7 | Frovatriptan Impurity 7. Grade: > 95%. Molecular formula: C15H19N3O. Mole weight: 257.34. | |
| Frovatriptan Impurity 7 | Frovatriptan Impurity 7. Uses: For analytical and research use. Molecular formula: C14H17N3O2. Mole weight: 259.31. Catalog: APB10492. | |
| Frovatriptan Impurity 8 | Frovatriptan Impurity 8. Grade: > 95%. Molecular formula: C13H25NO2. Mole weight: 227.35. | |
| Frovatriptan Impurity 8 | Frovatriptan Impurity 8. Uses: For analytical and research use. Molecular formula: C14H17N3O2. Mole weight: 259.31. Catalog: APB10491. | |
| Frovatriptan Impurity 9 | Frovatriptan Impurity 9. Uses: For analytical and research use. Molecular formula: C14H17N3O2. Mole weight: 259.31. Catalog: APB10490. | |
| Frovatriptan Impurity 9 | Frovatriptan Impurity 9. Grade: > 95%. Molecular formula: C14H16N2O2. Mole weight: 244.30. | |
| Frovatriptan Racemate | Frovatriptan Racemate is a combination of both the R and S enantiomers of Frovatriptanis, a drug for migraines and cluster headaches. Synonyms: (RS)-3-(Methylamino)-2,3,4,9-tetrahydro-1H-carbazole-6-carboxamide; 3-Methylamino-6-carboxamido-1,2,3,4-tetrahydrocarbazole; 2,3,4,9-Tetrahydro-3-(methylamino)-1H-carbazole-6-carboxamide. Grade: > 95%. CAS No. 147009-08-3. Molecular formula: C14H17N3O. Mole weight: 243.31. | |
| Frovatriptan Related Compound A | Frovatriptan Related Compound A. Uses: For analytical and research use. CAS No. 147008-88-6. Mole weight: 229.28. Catalog: AP147008886. | |
| Frovatriptan Succinate | Frovatriptan Succinate is a selective 5-hydroxytryptamine 1B/1D (5-HT1B/1D) receptor agonist (triptan) used for the acute treatment of migraine attacks with or without aura. It is marketed as the succinate salt and is distinguished among triptans by its notably long terminal half-life (approximately 26 hours), which provides sustained receptor engagement and may contribute to lower recurrence rates. Applications: Frovatriptan succinate is indicated for the acute treatment of migraine attacks with or without aura in adults. its long half-life makes it particularly suitable for patients experiencing migraines with prolonged duration or those with a history of migraine recurrence. Category: Active pharmaceutical ingredients. Synonyms: (3R)-2,3,4,9-Tetrahydro-3-(methylamino)-1H-carbazole-6-carboxamide butanedioate;1H-Carbazole-6-carboxamide, 2,3,4,9-tetrahydro-3-(methylamino)-, (3R)-, butanedioate. CAS No. 158930-09-7. Product ID: API158930097. Molecular formula: C18H23N3O5. Mole weight: 361.4. InChIKey: WHTHWNUUXINXHN-SBSPUUFOSA-N. |  |
| Frovatriptan Succinate | Thesuccinate salt form of Frovatriptan, a carbazole derivative, has been found to be a 5-HT receptor agonist that could be used as an antimigraine agent. Synonyms: (3R)-2,3,4,9-Tetrahydro-3-(methylamino)-1H-carbazole-6-carboxamide butanedioate; 1H-Carbazole-6-carboxamide, 2,3,4,9-tetrahydro-3-(methylamino)-, (3R)-, butanedioate (1:1); Sb-209509ax; Vml 251. Grade: > 95%. CAS No. 158930-09-7. Molecular formula: C18H23N3O5. Mole weight: 361.40. | |
| Frovatriptan succinate hydrate | Frovatriptan is a selective agonist of the 5-HT1B and 5-HT1D (Kis = 2.51 and 3.98 nM, respectively). Synonyms: SB 209509; VML 251; butanedioic acid, compd. with (R)-2,3,4,9-tetrahydro-3-(methylamino)-1H-carbazole-6-carboxamide, hydrate (1:1:1); R-(+) 3-Methylamino-6-carboxamido-1,2,3,4-tetrahydrocarbazole monosuccinate monohydrate. Grade: ≥98%. CAS No. 158930-17-7. Molecular formula: C14H17N3O·C4H6O4·H2O. Mole weight: 379.41. | |
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