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Mesoporphyrin IX (dihydrochloride) is a photosensitizer that can be used to modify liposomes. Mesoporphyrin IX (dihydrochloride) can insert into lipid vesicles and disrupt the viral membrane structure in vesicular stomatitis virus ( VSV ), inducing cross-linking of VSV glycoproteins, thereby inhibiting viral activity [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 68938-72-7. Pack Sizes: 1 mg. Product ID: HY-W073074.
N-methyl Mesoporphyrin IX
N-methyl Mesoporphyrin IX is a transition state analog of porphyrin and an inhibitor of ferrochelatase involved in heme synthesis. It has been used as a G-quadruplex DNA specific fluorescent probe for monitoring Aβ fibrillation in living cells. Synonyms: 3-[18-(2-carboxyethyl)-7,12-diethyl-3,8,13,17,22-pentamethyl-23H-porphyrin-2-yl]propanoic acid. Grades: ≥95%. CAS No. 142234-85-3. Molecular formula: C35H40N4O4. Mole weight: 580.72.
Zn(II) Mesoporphyrin IX
Zn(II) Mesoporphyrin IX (ZnMP) is a specific activator of ABCB10 , significantly increasing its ATPase activity and acting as a substrate for ABCB10 in heme synthesis. Zn(II) Mesoporphyrin IX may promote the transcription of hemoglobinization genes by facilitating the degradation of the Bach1 repressor. Zn(II) Mesoporphyrin IX aids in studying the potential roles of ABCB10 in heme synthesis, oxidative stress protection, hepatitis C, and other areas [1] [2]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: ZnMP. CAS No. 14354-67-7. Pack Sizes: 1 mg; 5 mg. Product ID: HY-W583212.
7,12-Diethyl-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropionic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2,4-diethyl-aniline; 2,4-Diethylbenzenamine; 2,4-Diaethyl-anilin; 2,4-Diethylanilin; 2,4-dimethylmethylaniline; 2,4-diethyldeuteroporphyrin; 4-Amino-1.3-diaethyl-benzol; 7,12-diethyl-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropionic acid; Mesoporphy. Product Category: Heterocyclic Organic Compound. CAS No. 493-90-3. Molecular formula: C34H38N4O4. Mole weight: 566.689920 [g/mol]. Purity: 0.96. IUPACName: 3-[18-(2-carboxyethyl)-8,13-diethyl-3,7,12,17-tetramethyl-22,23-dihydroporphyrin-2-yl]propanoic acid. Canonical SMILES: CCC1=C(C2=CC3=C(C(=C(N3)C=C4C(=C(C(=N4)C=C5C(=C(C(=N5)C=C1N2)C)CCC(=O)O)CCC(=O)O)C)C)CC)C. Density: 1.24 g/cm³. ECNumber: 207-782-4. Product ID: ACM493903. Alfa Chemistry ISO 9001:2015 Certified. Categories: Mesoporphyrin IX.
protoporphyrinogen oxidase
This is the last common enzyme in the biosynthesis of chlorophylls and heme. Two isoenzymes exist in plants: one in plastids and the other in mitochondria. This is the target enzyme of phthalimide-type and diphenylether-type herbicides. The enzyme from oxygen-dependent species contains FAD. Also slowly oxidizes mesoporphyrinogen IX. Group: Enzymes. Synonyms: protoporphyrinogen IX oxidase; protoporphyrinogenase; PPO; Protox; HemG; HemY. Enzyme Commission Number: EC 1.3.3.4. CAS No. 53986-32-6. 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-1378; protoporphyrinogen oxidase; EC 1.3.3.4; 53986-32-6; protoporphyrinogen IX oxidase; protoporphyrinogenase; PPO; Protox; HemG; HemY. Cat No: EXWM-1378.
Stannsoporfin
Stannsoporfin (SnMP) is a porphyrin-Sn(IV) complex, is also a potent heme oxygenase inhibitor, that inhibits HO-1-mediated heme catabolism with potential medicinal application for the treatment of both neonatal jaundice and inherited hyperbilirubinemia syndromes. It was developed to possess unique structural and photophysical properties that make it a particularly potent and bioavailable in vivo inhibitor suitable for clinical use in newborns and studies to date have revealed a very favorable therapeutic profile with no significant adverse side effects. Synonyms: Tin mesoporphyrin; SNMPP; SnMP; Sn Mesoporphyrin; Stanate; Sn(IV) Mesoporphyrin IX Dichloride. CAS No. 106344-20-1. Molecular formula: C34H36Cl2N4O4Sn. Mole weight: 754.29.
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