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| Product | Description | |
|---|---|---|
| Proteoglycan from bovine nasal septum | chromatographically purified. Group: Fluorescence/luminescence spectroscopy. |  |
| Proteoglycan from chicken sternal cartilage | solid. Group: Fluorescence/luminescence spectroscopy. | |
| Protheobromine | Protheobromine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Protheobromine, Cordaleromin, Pantobromino, Protheobromin, Cordabromin, Vascopil, Bonicor, Corodil, Theocor, Proteobromina, Protheobrominum, Pro-Cor, TEBE, beta-Oxypropyltheobromine, Protheobromine [INN], Proteobromina [INN-Spanish], Protheobrominum [INN-Latin], 1-(2-Hydroxypropyl)theobromine, l-(beta-Hydroxypropyl)theobromine, EINECS 200-034-8. Product Category: Heterocyclic Organic Compound. CAS No. 50-39-5. Molecular formula: C10H14N4O3. Mole weight: 238.246. Purity: 0.96. IUPACName: 1-(2-hydroxypropyl)-3,7-dimethylpurine-2,6-dione. Canonical SMILES: CC(CN1C(=O)C2=C(N=CN2C)N(C1=O)C)O. Density: 1.46g/cm³. ECNumber: 200-034-8. Product ID: ACM50395. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Prothioconazole | analytical standard. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. | |
| Prothioconazole | 1g Pack Size. Group: Analytical Reagents, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C14H15Cl2N3OS. CAS No. 178928-70-6. Prepack ID 90023720-1g. Molecular Weight 344.2594. See USA prepack pricing. |  |
| Prothioconazole | Prothioconazole is a triazolinthione fungicide. Prothioconazole is a CYP51 inhibitor [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: JAU-6476. CAS No. 178928-70-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-116568. |  |
| Prothioconazole-desthio | analytical standard. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. | |
| Prothionamide | Protionamide (prothionamide) acts on tuberculosis and leprosy. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Protionamide. CAS No. 14222-60-7. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-B0306. | |
| Prothionamide | Prothionamide. Group: Biochemicals. Alternative Names: 2-propyl -4-pyridinecarbothioamide ; 2-propyl thioisonicotinamide; 2-propyl isonicotinylthioamide. Grades: Highly Purified. CAS No. 14222-60-7. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C9H12N2S. US Biological Life Sciences. |  Worldwide |
| Prothionamide-[d5] | Prothionamide-[d5] is the labelled analogue of Protionamide. Protionamide is a drug used in the treatment of tuberculosis and leprosy. Synonyms: Prothionamide D5. Grade: 95% by HPLC; 95% atom D. CAS No. 1330261-26-1. Molecular formula: C9H7D5N2S. Mole weight: 185.30. |  |
| Prothionamide sulfoxide | Prothionamide sulfoxide. Group: Biochemicals. Alternative Names: 2-Propyl-a-sulfinyl-4-pyridinemethanamine; 2-Propyl-4-pyridinecarbothioamide S-oxide. Grades: Highly Purified. CAS No. 62178-61-4. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C9H12N2OS. US Biological Life Sciences. | Worldwide |
| Prothipendyl-[d6]-oxalate | Prothipendyl-[d6]-oxalate is a labelled salt of Prothipendyl. Prothipendyl is a weak dopamine receptor antagonist that is used to treat anxiety and agitation in psychotic syndromes. Synonyms: 10-{3-[Di(methyl-d3)amino]propyl}-10H-pyrido[3,2-b][1,4]benzothiazine oxalate salt; N,N-Di(methyl-d3)-3-pyrido[3,2-b][1,4]benzothiazin-10-ylpropan-1-amine oxalate salt; (3-Benzo[b]pyrido[2,3-e][1,4]thiazin-10-yl-propyl)-dimethyl-D6-amine oxalate. Grade: 95% by HPLC; 98% atom D. Molecular formula: C18H15D6N3O4S. Mole weight: 381.48. | |
| Prothipendyl-(dimethyl-d6) oxalate | analytical standard. Group: Antihistamines standards. | |
| Prothipendyl hydrochloride | Prothipendyl hydrochloride. Group: Biochemicals. Alternative Names: N,N-Dimethyl-10H-pyrido[3,2-b][1,4]benzothiazine-10-propanamine hydrochloride; AY 56031; Azacon. Grades: Highly Purified. CAS No. 1225-65-6. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C16H20ClN3S. US Biological Life Sciences. | Worldwide |
| Prothracarcin | Prothracarcin is an antitumor antibiotic produced by Str. umbrosus subsp. raffinophilus DO-62. It is active against Gram-positive and Gram-negative bacteria and experimental murine tumor sarcoma 180 and leukemia P388. Synonyms: Antibiotic DC 62. Grade: >98%. CAS No. 81542-99-6. Molecular formula: C14H14N2O. Mole weight: 226.27. | |
| PROT-IN-1 | PROT-IN-1 (Compound 2) is a proline transporter ( PROT ) inhibitor ( IC 50 : 1.48 μM). PROT-IN-1 can be used for research of cognitive disorders [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 329935-45-7. Pack Sizes: 5 mg; 10 mg. Product ID: HY-153763. | |
| Protionamide | An anti-tuberculosis agent. It has also been used to treat Leprosy. Antibacterial (tuberculostatic). Group: Biochemicals. Alternative Names: 2-propyl -4-pyridinecarbothioamide ; 2-propyl thioisonicotinamide; 2-propyl isonicotinylthioamide; 9778 R. P.; Ektebin; Prothionamide; Protion; Protionamid; Protionizina; RP 9778; TH 1321; Tebeform; Trevintix; Tuberex. Grades: Highly Purified. CAS No. 14222-60-7. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Protionamide | 5g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Pyridines, Pyrimidines. Formula: C9H12N2S. CAS No. 14222-60-7. Prepack ID 89981934-5g. Molecular Weight 180.27. See USA prepack pricing. | |
| Protionamide Sulfoxide-[d5] | Protionamide Sulfoxide-[d5] is the labelled analogue of Protionamide Sulfoxide, which is a metabolite of Protionamide. Protionamide is a drug used in the treatment of tuberculosis and leprosy. Synonyms: Protionamide-d5 Sulfoxide; 2-(Propyl-d5)-α-sulfinyl-4-pyridinemethanamine; 2-(Propyl-d5)-4-pyridinecarbothioamide S-Oxide; 2-(Propyl-d5)thioisonicotinamide S-Oxide; Prothionamide-d5 S-Oxide. Grade: >95%. CAS No. 1329568-86-6. Molecular formula: C9H7D5N2OS. Mole weight: 201.30. | |
| Protirelin | Protirelin. Uses: For analytical and research use. Group: Api standards; european pharmacopoeia (ph. eur.); pharmaceutical toxicology; pharmacopoeial standards. Alternative Names: Thyrotropic hormone-releasing factor, L-Pyroglutamyl-L-histidyl-L-proline amide, Lopremone, Synthetic thyrotropin-releasing hormone, Antepan, Synthetic thyrotropin-releasing factor, TRF, Thyrotropic releasing hormone, Stimu TSH, Thyrotropin-releasing hormone, Synthetic TRH, L-Prolinamide, 5-oxo-L-prolyl-L-histidyl-, (Pyro)-L-glutamic acid-L-histidine-L-proline-NH2, 83: PN: US20090175821 PAGE: 403 claimed protein, TSH-RF, Rifotironin, Thyroliberin, Prem, Thyrotropin-releasing factor (8CI), Synthetic TSH-releasing hormone, TRH, Protirelin, Thyrefact, Thyrotropic-releasing factor, FDA 1725, Synthetic TSH-releasing factor, Thypinone, L-Pyroglutamyl-L-histidyl-L-prolinamide, Synthetic TRF,Protirelin, Relefact TRH, Ro 8-6270/9, 5-Oxo-l-prolyl-l-histidyl-l-prolinamide, Abbott 38579, Rifathyroin, Thyroid-stimulating hormone-releasing factor, TSH-releasing hormone, Thyroid releasing hormone, 252: PN: WO2010033207 SEQID: 378 claimed protein, TSH-releasing factor, Thyrotropic hormone-releasing hormone. CAS No. 24305-27-9. IUPAC Name: (2S)-N-[(2S)-1-[(2S)-2-carbamoylpyrrolidin-1-yl]-3-(1H-imidazol-4-yl)-1-oxopropan-2-yl]-5-oxopyrrolidine-2-carboxamide. Molecular formula: C16H22N6O4. Mole weight: 362.38. Catalog: APS24305279. SMILES: NC(=O)[C@@H]1CCCN1C(=O)[C@H]( | |
| Protirelin | Protirelin is a highly conserved neuropeptide that exerts the hormonal control of thyroid-stimulating hormone (TSH) levels as well as neuromodulatory functions. Uses: Scientific research. Group: Peptides. Alternative Names: Thyrotropin-releasing-hormone; TRH. CAS No. 24305-27-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P0002. | |
| Protirelin acetate | Protirelin Acetate is a highly conserved neuropeptide that exerts the hormonal control of thyroid-stimulating hormone (TSH) levels as well as neuromodulatory functions. Uses: Scientific research. Group: Peptides. Alternative Names: Thyrotropin-releasing-hormone acetate; TRH acetate. CAS No. 120876-23-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-P0002A. | |
| Protirelin Acetate | Protirelin Acetate is a highly conserved neuropeptide that plays a hormonal role in controlling thyroid-stimulating hormone (TSH) levels and neuromodulatory functions. Synonyms: TRF Acetate; TRH Acetate; TSH-RF Acetate; pGlu-HP-NH2; L-pyroglutamyl-L-histidyl-L-prolinamide acetic acid; 5-Oxo-L-prolyl-L-histidyl-L-prolinamide acetate (2:3). Grade: ≥95%. CAS No. 120876-23-5. Molecular formula: C16H22N6O4.3/2C2H4O2. Mole weight: 452.46. | |
| PROTO-1 | PROTO-1 is a hair cell protector and can be used in studies of ototoxicity-induced hair cell death [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 312951-85-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-18673. | |
| protoaphin-aglucone dehydratase (cyclizing) | The product is converted non-enzymically to erythroaphin, an aphid pigment. Group: Enzymes. Synonyms: protoaphin dehydratase; protoaphin dehydratase (cyclizing); protoaphin-aglucone hydro-lyase (cyclizing). Enzyme Commission Number: EC 4.2.1.73. CAS No. 64177-87-3. 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-5057; protoaphin-aglucone dehydratase (cyclizing); EC 4.2.1.73; 64177-87-3; protoaphin dehydratase; protoaphin dehydratase (cyclizing); protoaphin-aglucone hydro-lyase (cyclizing). Cat No: EXWM-5057. |  |
| Protoapigenone | Protoapigenone is an antineoplastic agent isolated from ferns. Protoapigenone has significant inhibitory activity against Hep G2, Hep 3B, MCF-7, A549 and MDAMB-231, with IC 50 s values of 1.60, 0.23, 0.78, 3.88 and 0.27 μg/mL respectively [1]. Uses: Scientific research. Group: Natural products. CAS No. 862884-32-0. Pack Sizes: 1 mg; 5 mg. Product ID: HY-134008. | |
| protoasukamycin 4-monooxygenase | The enzyme, characterized from the bacterium Streptomyces nodosus subsp. asukaensis, is involved in the biosynthesis of the antibiotic asukamycin. Requires a flavin cofactor, with no preference among FMN, FAD or riboflavin. When flavin concentration is low, activity is enhanced by the presence of the NADH-dependent flavin-reductase AsuE2. Group: Enzymes. Enzyme Commission Number: EC 1.14.13.215. 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-0817; protoasukamycin 4-monooxygenase; EC 1.14.13.215. Cat No: EXWM-0817. | |
| Protocatechualdehyde | Protocatechualdehyde (Catechaldehyde), a natural polyphenol compound isolated from the roots of radix Salviae Miltiorrhizae, is associated with a wide variety of biological activities and has been widely used in medicine as an antioxidant, anti-aging, an antibacterial and anti-inflammatory agent. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1,2-Dihydroxy-4-formylbenzene. Product Category: Inhibitors. Appearance: Slightly brown crystalline powder. CAS No. 139-85-5. Molecular formula: C7H6O3. Mole weight: 138.12. Purity: 0.98. IUPACName: 3,4-Dihydroxybenzaldehyde. Canonical SMILES: C1=CC(=C(C=C1C=O)O)O. Density: 1.2667 g/cm³. Product ID: ACM139855. Alfa Chemistry ISO 9001:2015 Certified. | |
| Protocatechualdehyde | Protocatechualdehyde (Catechaldehyde), a natural polyphenol compound isolated from the roots of radix Salviae Miltiorrhizae , is associated with a wide variety of biological activities and has been widely used in medicine as an antioxidant, anti-aging, an antibacterial and anti-inflammatory agent [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Catechaldehyde; Protocatechuic aldehyde; Rancinamycin IV. CAS No. 139-85-5. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N0295. | |
| Protocatechualdehyde | Protocatechualdehyde. Group: Biochemicals. Alternative Names: 3,4-Dihydroxybenzaldehyde; Protocatechuic aldehyde; Rancinamycin IV. Grades: Plant Grade. CAS No. 139-85-5. Pack Sizes: 100mg. Molecular Formula: C7H6O3, Molecular Weight: 138.121. US Biological Life Sciences. | Worldwide |
| protocatechuate 3,4-dioxygenase | Requires Fe3+. The enzyme, which participates in the degradation of aromatic compounds, catalyses the intradiol addition of both oxygen atoms from molecular oxygen, resulting in ortho-cleavage of the aromatic ring. The type of cleavage leads to mineralization via the intermediate 3-oxoadipate. Group: Enzymes. Synonyms: protocatechuate oxygenase; protocatechuic acid oxidase; protocatechuic 3,4-dioxygenase; protocatechuic 3,4-oxygenase; protocatechuate:oxygen 3,4-oxidoreductase (decyclizing). Enzyme Commission Number: EC 1.13.11.3. CAS No. 9029-47-4. Protocatechuate 3, 4-dioxygenase. 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-0549; protocatechuate 3,4-dioxygenase; EC 1.13.11.3; 9029-47-4; protocatechuate oxygenase; protocatechuic acid oxidase; protocatechuic 3,4-dioxygenase; protocatechuic 3,4-oxygenase; protocatechuate:oxygen 3,4-oxidoreductase (decyclizing). Cat No: EXWM-0549. | |
| Protocatechuate 3,4-dioxygenase | Protocatechuate 3,4-dioxygenase is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Signaling pathways. CAS No. 9029-47-4. Pack Sizes: 25 U. Product ID: HY-P2915. | |
| Protocatechuate 3,4-Dioxygenase from Bacteria, Recombinant | In enzymology, a protocatechuate 3,4-dioxygenase (EC 1.13.11.3) is an enzyme that catalyzes the chemical reaction:3,4-dihydroxybenzoate + O2<-> 3-carboxy-cis,cis-muconate. Thus, the two substrates of this enzyme are 3,4-dihydroxybenzoate (protocatechuic acid) and O2, whereas its product is 3-carboxy-cis,cis-muconate. This enzyme belongs to the family of oxidoreductases, specifically those acting on single donors with O2 as oxidant and incorporation of two atoms of oxygen into the substrate (oxygenases). This enzyme participates in benzoate degradation via hydroxylation and 2,4-dichlorobenzoate degradation. It employs one cofactor, iron. Applications: Useful for removal of protocatechuate derived from choline esterase determination. Group: Enzymes. Synonyms: protocatechuate 3,4-dioxygenase; protocatechuate oxygenase; protocatechuic acid oxidase; protocatech. Enzyme Commission Number: EC 1.13.11.3. CAS No. 9029-47-4. Protocatechuate 3, 4-dioxygenase. Mole weight: 28 kD α subuit, 24 kD β subunit?SDS-PAGE?. Activity: > 3 Units / mg. Storage: 1 - 10°C (do not freeze). Form: Solution. Source: E. coli. Species: Bacteria. protocatechuate 3,4-dioxygenase; protocatechuate oxygenase; protocatechuic acid oxidase; protocatechuic 3,4-dioxygenase; protocatechuic 3,4-oxygenase; 9029-47-4; EC 1.13.11.3; PCD. Cat No: NATE-1028. | |
| protocatechuate 4,5-dioxygenase | Requires Fe2+. Group: Enzymes. Synonyms: protocatechuate 4,5-oxygenase; protocatechuic 4,5-dioxygenase; protocatechuic 4,5-oxygenase; protocatechuate:oxygen 4,5-oxidoreductase (decyclizing). Enzyme Commission Number: EC 1.13.11.8. CAS No. 9029-56-5. 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-0600; protocatechuate 4,5-dioxygenase; EC 1.13.11.8; 9029-56-5; protocatechuate 4,5-oxygenase; protocatechuic 4,5-dioxygenase; protocatechuic 4,5-oxygenase; protocatechuate:oxygen 4,5-oxidoreductase (decyclizing). Cat No: EXWM-0600. | |
| protocatechuate decarboxylase | This enzyme belongs to the family of lyases, specifically the carboxy-lyases, which cleave carbon-carbon bonds. This enzyme participates in benzoate degradation via hydroxylation. Group: Enzymes. Synonyms: 3,4-dihydrobenzoate decarboxylase; protocatechuate carboxy-lyase. Enzyme Commission Number: EC 4.1.1.63. CAS No. 37290-55-4. 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-4810; protocatechuate decarboxylase; EC 4.1.1.63; 37290-55-4; 3,4-dihydrobenzoate decarboxylase; protocatechuate carboxy-lyase. Cat No: EXWM-4810. | |
| Protocatechuic acid | Protocatechuic acid is a phenolic compound which exhibits neuroprotective effect. Uses: Scientific research. Group: Natural products. Alternative Names: 3,4-Dihydroxybenzoic acid. CAS No. 99-50-3. Pack Sizes: 10 mM * 1 mL; 200 mg; 1 g. Product ID: HY-N0294. | |
| Protocatechuic acid | primary reference standard. Group: Herbal medicinal products standards. | |
| Protocatechuic acid | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Protocatechuic Acid | Protocatechuic Acid - Product ID: NST-10-36. Category: Benzoic acid derivatives. Alternative Names: 3,4-Dihydroxybenzoic acid. Purity: 98%. Test method: HPLC. CAS No. 99-50-3. Pack Sizes: 50g, 100g, 250g, 500g. Appearance: White to off-white powder. Molecular formula: C7H6O4. Mole weight: 154.12. Storage: +2 +8 °C. |  |
| Protocatechuic Acid | Protocatechuic Acid. Group: Biochemicals. Alternative Names: Carbohydroquinonic acid; Catechol-4-carboxylic acid; Hypogallic acid. Grades: Plant Grade. CAS No. 99-50-3. Pack Sizes: 20mg. Molecular Formula: C7H6O4, Molecular Weight: 154.12. US Biological Life Sciences. | Worldwide |
| Protocatechuic acid (Standard) | Protocatechuic acid (Standard) is the analytical standard of Protocatechuic acid. This product is intended for research and analytical applications. Protocatechuic acid is a phenolic compound which exhibits neuroprotective effect. Uses: Scientific research. Group: Natural products. CAS No. 99-50-3. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0294R. | |
| Protocetraric acid | Protocetraric acid has strong antioxidant, antibacterial and anticancer effects. Synonyms: 11H-Dibenzo(b,e)(1,4)dioxepin-7-carboxylic acid, 4-formyl-3,8-dihydroxy-9-(hydroxymethyl)-1,6-dimethyl-11-oxo-; 10-formyl-3,9-dihydroxy-4-(hydroxymethyl)-1,7-dimethyl-6-oxobenzo[b][1,4]benzodioxepine-2-carboxylic acid; Protocetrarsaeure. Grade: ≥98%. CAS No. 489-51-0. Molecular formula: C18H14O9. Mole weight: 374.30. | |
| protochlorophyllide reductase | The enzyme catalyses a light-dependent trans-reduction of the D-ring of protochlorophyllide; the product has the (7S,8S)-configuration. Group: Enzymes. Synonyms: NADPH2-protochlorophyllide oxidoreductase; NADPH-protochlorophyllide oxidoreductase; NADPH-protochlorophyllide reductase; protochlorophyllide oxidoreductase (ambiguous); protochlorophyllide photooxidoreductase; light-dependent protochlorophyllide reductase. Enzyme Commission Number: EC 1.3.1.33. CAS No. 68518-04-7. 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-1306; protochlorophyllide reductase; EC 1.3.1.33; 68518-04-7; NADPH2-protochlorophyllide oxidoreductase; NADPH-protochlorophyllide oxidoreductase; NADPH-protochlorophyllide reductase; protochlorophyllide oxidoreductase (ambiguous); protochlorophyllide photooxidoreductase; light-dependent protochlorophyllide reductase. Cat No: EXWM-1306. | |
| Protodeltonin | Protodeltonin. Group: Biochemicals. Grades: Plant Grade. CAS No. 94992-08-2. Pack Sizes: 10mg. Molecular Formula: C51H84O23, Molecular Weight: 1065.21. US Biological Life Sciences. | Worldwide |
| protodeoxyviolaceinate monooxygenase | The enzyme, characterized from the bacterium Chromobacterium violaceum, participates in the biosynthesis of the violet pigment violacein. The product, protoviolaceinate, can be acted upon by EC 1.14.13.224, violacein synthase, leading to violacein production. However, it is very labile, and in the presence of oxygen can undergo non-enzymic autooxidation to the shunt product proviolacein. Group: Enzymes. Synonyms: vioD (gene name); protoviolaceinate synthase. Enzyme Commission Number: EC 1.14.13.217. 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-0819; protodeoxyviolaceinate monooxygenase; EC 1.14.13.217; vioD (gene name); protoviolaceinate synthase. Cat No: EXWM-0819. | |
| Protodioscin | Protodioscin. Group: Biochemicals. Alternative Names: Saponin C. Grades: Plant Grade. CAS No. 55056-80-9. Pack Sizes: 20mg. Molecular Formula: C51H84O22, Molecular Weight: 1049.2. US Biological Life Sciences. | Worldwide |
| Protodioscin | Protodioscin, a major steroidal saponin in Trigonella foenum-graecum Linn., has been shown to exhibit multiple biological actions, such as anti-hyperlipidemia, anti-cancer, sexual effects and cardiovascular properties. Uses: Scientific research. Group: Natural products. CAS No. 55056-80-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0799. | |
| Protodioscin | Protodioscin - Product ID: NST-10-58. Category: Sterols. Purity: 98%. Test method: HPLC. CAS No. 55056-80-9. Pack Sizes: 0,05g, 0,1g, 0,25g, 0,5g. Appearance: White to beige colored powder. Molecular formula: C51H84O22. Mole weight: 1049.2. Storage: +2 +8 °C. | |
| protodioscin 26-O-β-D-glucosidase | The enzyme has been characterized from the plants Cheilocostus speciosus and Solanum torvum. It also hydrolyses the 26-β-D-glucose group from related steroid glucosides such as protogracillin, torvoside A and torvoside H. Group: Enzymes. Synonyms: F26G; torvosidase; CSF26G1; furostanol glycoside 26-O-β-D-glucosidase; furostanol 26-O-β-D-glucoside glucohydrolase. Enzyme Commission Number: EC 3.2.1.186. 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-3870; protodioscin 26-O-β-D-glucosidase; EC 3.2.1.186; F26G; torvosidase; CSF26G1; furostanol glycoside 26-O-β-D-glucosidase; furostanol 26-O-β-D-glucoside glucohydrolase. Cat No: EXWM-3870. | |
| Protogracillin | Protogracillin. Group: Biochemicals. Grades: Plant Grade. CAS No. 54848-30-5. Pack Sizes: 10mg. Molecular Formula: C51H84O23, Molecular Weight: 1065.21. US Biological Life Sciences. | Worldwide |
| Protoneogracillin | Protoneogracillin, a furostanol glycoside, shows anti-fungal activity against the plant pathogenic fungus P.oryzae (MMDC=94.0 μM) and cytotoxic activity on K562 cancer cells (IC50=6.6 μM). Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Solid. CAS No. 191334-50-6. Molecular formula: C51H84O23. Mole weight: 1065.2. Canonical SMILES: C[C@@]12[C@](C[C@@]3([H])[C@]2([H])[C@@H]([C@](O)(O3)CC[C@H](C)CO[C@@H]4O[C@@H]([C@H]([C@@H]([C@H]4O)O)O)CO)C)([H])[C@@]5([H])[C@]([C@@]6(C(C[C@H](CC6)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO)O)O[C@@H]8O[C@@H]([C@H]([C@@H]([C@H]8O)O)O)CO)O[C@H]9[C@@H]([C@@H]([C@H]([C@@H](O9)C)O)O)O)=CC5)C)([H])CC1. Product ID: ACM191334506. Alfa Chemistry ISO 9001:2015 Certified. | |
| proton-translocating NAD(P)+ transhydrogenase | The enzyme is a membrane bound proton-translocating pyridine nucleotide transhydrogenase that couples the reversible reduction of NADP by NADH to an inward proton translocation across the membrane. In the bacterium Escherichia coli the enzyme provides a major source of cytosolic NADPH. Detoxification of reactive oxygen species in mitochondria by glutathione peroxidases depends on NADPH produced by this enzyme. Group: Enzymes. Synonyms: pntA (gene name); pntB (gene name); NNT (gene name). Enzyme Commission Number: EC 7.1.1.1 (Formerly EC 1.6.1.5). 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-1578; proton-translocating NAD(P)+ transhydrogenase; EC 1.6.1.5; pntA (gene name); pntB (gene name); NNT (gene name). Cat No: EXWM-1578. | |
| Proto-oncogene PIM1 (191-199) | Proto-oncogene PIM1 (191-199) is a 9-aa peptide. Pim-1's role in oncogenic signalling has led to it becoming a widely studied target in cancer research, with numerous drug candidates under investigation which target it. | |
| Protopanaxadiol, 20S- | Protopanaxadiol, 20S-. Group: Biochemicals. CAS No. 30636-90-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| protopanaxadiol 6-hydroxylase | A heme-thiolate protein (P-450). Involved in the biosynthetic pathway of ginsenosides. Isolated from the rhizomes of ginseng (Panax ginseng). Group: Enzymes. Synonyms: protopanaxatriol synthase; P6H; CYP716A53v2; protopanaxadiol,NADPH:O2 oxidoreductase (6α-hydroxylating). Enzyme Commission Number: EC 1.14.13.184. 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-0783; protopanaxadiol 6-hydroxylase; EC 1.14.13.184; protopanaxatriol synthase; P6H; CYP716A53v2; protopanaxadiol,NADPH:O2 oxidoreductase (6α-hydroxylating). Cat No: EXWM-0783. | |
| Protopanaxatriol | 20S-Protopanaxatriol (g-PPT), a dammarane-type tetracyclic terpene sapogenin, may be used to study its binding to and modulation of cell function via glucocortoid (GR) and oestrogen (ER) receptors. Protopanaxatriol can be used in health products. Synonyms: 20(S)-APPT; g-PPT. Grade: >98%. CAS No. 34080-08-5. Molecular formula: C30H52O4. Mole weight: 476.73. | |
| Protopanaxatriol | Botanical Source: Group: Biochemicals. Alternative Names: (20R)-Protopanaxatriol. Grades: Plant Grade. CAS No. 1453-93-6. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Protopanaxatriol, 20S- | Protopanaxatriol, 20S-. Group: Biochemicals. CAS No. 34080-08-5. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Protopine | Protopine (Corydinine), an isoquinoline alkaloid, is a specific reversible and competitive inhibitor of acetylcholinesterase. Protopine exhibits anti-inflammation, anti-microbial, anti-angiogenic and anti-tumour activity [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Corydinine. CAS No. 130-86-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0793. | |
| Protopine | Protopine is an alkaloid isolated from the tubers of Corydalis yanhusuo W.T.Wang. It shows weak spasmolytic, smooth muscle stimulant activities. Uses: Bactericidal; sedative; antihypertensive. Synonyms: 7-Methyl-6,8,9,16-tetrahydrodi[1,3]benzodioxolo[4,5-c:5,6-g]azecin-15(7H)-one; Biflorine. Grade: 98%. CAS No. 130-86-9. Molecular formula: C20H19NO5. Mole weight: 353.4. | |
| Protopine | Protopine is a Ca2+ channel blocker and antiplatelet agent. Immunomodulator. Group: Biochemicals. Alternative Names: 4,6,7,14-Tetrahydro-5-methyl-. Grades: Highly Purified. CAS No. 130-86-9. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| protopine 6-monooxygenase | A heme-thiolate protein (P-450) involved in benzophenanthridine alkaloid synthesis in higher plants. Group: Enzymes. Synonyms: protopine 6-hydroxylase. Enzyme Commission Number: EC 1.14.13.55. CAS No. 128561-60-4. 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-0862; protopine 6-monooxygenase; EC 1.14.13.55; 128561-60-4; protopine 6-hydroxylase. Cat No: EXWM-0862. | |
| Protopine hydrochloride | ?98%, solid. Group: Fluorescence/luminescence spectroscopy. | |
| Protopine N-Oxide | Protopine N-Oxide. Uses: For analytical and research use. Group: Impurity standards. CAS No. 87264-51-5. Molecular formula: C20H19NO6. Mole weight: 369.37. Catalog: APS87264515. SMILES: C[N+]1([O-])CCc2cc3OCOc3cc2C(=O)Cc4ccc5OCOc5c4C1. Format: Neat. Shipping: Room Temperature. | |
| Protoporphyrinato zinc | Protoporphyrinato zinc. Group: other materials. Alternative Names: PROTOPORPHYRINATO ZINC; dihydrogen [3, 8, 13, 17-tetramethyl-7, 12-divinyl-21H, 23H-porphine-2, 18-dipropionato(4-)-N21, N22, N23, N24]zincate(4-); Zinc protoporphyrin trihydrate; Zinc protoporphyrin trihydrate, 95+%. CAS No. 15442-64-5. Product ID: zinc; 3-[18-(2-carboxyethyl)-8,13-bis(ethenyl)-3,7,12,17-tetramethylporphyrin-21,23-diid-2-yl]propanoic acid. Molecular formula: 626g/mol. Mole weight: C34H32N4O4Zn. CC1=C (C2=CC3=NC (=CC4=C (C (=C ([N-]4)C=C5C (=C (C (=N5)C=C1[N-]2)C)C=C)C)C=C)C (=C3CCC (=O)O)C)CCC (=O)O. [Zn+2]. InChI=1S/C34H34N4O4. Zn/c1-7-21-17 (3)25-13-26-19 (5)23 (9-11-33 (39)40)31 (37-26)16-32-24 (10-12-34 (41)42)20 (6)28 (38-32)15-30-22 (8-2)18 (4)27 (36-30)14-29 (21)35-25; /h7-8, 13-16H, 1-2, 9-12H2, 3-6H3, (H4, 35, 36, 37, 38, 39, 40, 41, 42); /q; +2/p-2. FUTVBRXUIKZACV-UHFFFAOYSA-L. |  |
| protoporphyrin ferrochelatase | The enzyme catalyses the terminal step in the heme biosynthesis pathways of eukaryotes and Gram-negative bacteria. Group: Enzymes. Synonyms: ferro-protoporphyrin chelatase; iron chelatase (ambiguous); heme synthetase (ambiguous); heme synthase (ambiguous); protoheme ferro-lyase; ferrochelatase (ambiguous). Enzyme Commission Number: EC 4.99.1.1. CAS No. 9012-93-5. 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-5358; protoporphyrin ferrochelatase; EC 4.99.1.1; 9012-93-5; ferro-protoporphyrin chelatase; iron chelatase (ambiguous); heme synthetase (ambiguous); heme synthase (ambiguous); protoheme ferro-lyase; ferrochelatase (ambiguous). Cat No: EXWM-5358. | |
| Protoporphyrin IX | Protoporphyrin IX. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Protoporphyrin; Ooporphyrin. Product Category: Porphyrins and Phthalocyanines. Appearance: Purple powder. CAS No. 553-12-8. Molecular formula: C34H34N4O4. Mole weight: 562.67. Purity: 0.95. IUPACName: 3-[18-(2-carboxyethyl)-8,13-bis(ethenyl)-3,7,12,17-tetramethyl-22,23-dihydroporphyrin-2-yl]propanoic acid. Product ID: ACM553128-3. Alfa Chemistry ISO 9001:2015 Certified. | |
| Protoporphyrin IX | ?95%. Group: Fluorescence/luminescence spectroscopy. | |
| Protoporphyrin IX | Protoporphyrin IX is a final intermediate in the heme biosynthetic pathway, which acts as a radiation sensitizer enhancing ROS generation even in a hypoxic state and inducing DNA damage. Protoporphyrin IX also acts as a photo sensitizer undergoing photobleaching that occurs through direct degradation by light irradiation. Protoporphyrin IX is formed and accumulated following 5-aminolevulinic acid (5-ALA) (HY-W000450) administration in the tumor cells of rats. Protoporphyrin IX causes selective improvement of basal cell carcinoma when activated red fluorescence of a peak wavelength at 405 nm. Protoporphyrin IX is promising for research of sonodynamic and photodynamic agents for a wide range of cancers, such as bladder cancer and nodular basal cell carcinoma [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. CAS No. 553-12-8. Pack Sizes: 100 mg; 250 mg. Product ID: HY-B1247. | |
| Protoporphyrin IX | Protoporphyrin IX is an important precursor to biologically essential prosthetic groups such as heme, cytochrome c, and chlorophylls. As a result, a number of organisms are able to synthesize this tetrapyrrole from basic precursors such as glycine and succinyl CoA, or glutamate. Despite the wide range of organisms that synthesize protoporphyrin IX the process is largely conserved from bacteria to mammals with a few distinct exceptions in higher plants.[1][2][3]. Group: Biochemicals. Alternative Names: 3,18-Divinyl-2,7,13,17-tetramethylporphine-8, 12-dipropionic acid. Grades: Reagent Grade. CAS No. 553-12-8. Pack Sizes: 100mg, 250mg, 1g, 5g. US Biological Life Sciences. | Worldwide |
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