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PROTOPORPHYRINATO ZINC

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PROTOPORPHYRINATO ZINC Basic information
Product Name:PROTOPORPHYRINATO ZINC
Synonyms: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+%;Zinc (II) Protoporphyrin IX - CAS 15442-64-5 - Calbiochem;PROTOPORPHYRINATO ZINC ISO 9001:2015 REACH;Zinc Protoporphyrin IX DISCONTINUED, offer Z439970;Zinc(II) 3,3'-(3,8,13,17-tetramethyl-7,12-divinylporphyrin-2,18-diyl)dipropionate
CAS:15442-64-5
MF:C34H31N4O4Zn-
MW:625.03
EINECS:239-455-7
Product Categories:Natural Porphyrins and Derivitives;Porphyrins;metal porphine (porphyrin) complex;1
Mol File:15442-64-5.mol
PROTOPORPHYRINATO ZINC Structure
PROTOPORPHYRINATO ZINC Chemical Properties
RTECS ZG9210300
storage temp. Inert atmosphere,2-8°C
solubility DMSO : 50 mg/mL (79.87 mM; Need ultrasonic)H2O : < 0.1 mg/mL (insoluble)
form Crystalline
color Dark red to purple
Water Solubility Insoluble in water. Soluble in ethanol, and DMSO, pyridine, or dimethyl formamide.
λmax426 nm
ε(extinction coefficient)≥10000 at 585-591nm in pyridine
≥12000 at 548-554nm in pyridine
≥135000 at 423-429nm in pyridine
Stability:Hygroscopic
InChIKeyFUTVBRXUIKZACV-RGGAHWMASA-K
SMILESC(C1C(=C2C=C3C(C=C)=C(C)C4C=C5C(C=C)=C(C)C6=CC7C(C)=C(CCC(=O)[O-])C8N=7[Zn+2]([N-]56)(N3=4)[N-]2C=1C=8)C)CC(=O)[O-].[H+]
EPA Substance Registry SystemZincate(2-), [7,12-diethenyl-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropanoato(4-)-.kappa.N21,.kappa.N22,.kappa.N23,.kappa.N24]-, dihydrogen, (SP-4-2)- (15442-64-5)
Safety Information
WGK Germany 3
TSCA TSCA listed
Storage Class11 - Combustible Solids
MSDS Information
PROTOPORPHYRINATO ZINC Usage And Synthesis
UsesZinc Protoporphyrin is a metabolite formed during biosynthesis and is used to evaluate iron nutrition and metabolism.
General DescriptionA potent and selective inhibitor of heme oxygenase, the enzyme which generates carbon monoxide (CO) and biliverdin. Inhibits soluble guanylyl cyclase and produces a time- and concentration-dependent inactivation of all three isoforms of nitric oxide synthase (IC50 = 800 nM, 4 μM, and 5 μM for nNOS, iNOS, and eNOS, respectively). Inhibits relaxation induced by acetylcholine, ANP, and VIP in isolated rat aorta. Blocks interleukin-1 and prevents induction of long-term potentiation. Also useful as an indicator of iron-deficient erythropoiesis. Does not cross the blood-brain barrier.
Biological ActivityInhibitor of heme oxygenase, which generates the putative neurotransmitter CO.
Biochem/physiol ActionsPrimary Targetheme oxygenase
in vivo

Zinc Protoporphyrin (12.5, 25, 50 mg/kg for i.p.; 12.5, 50 mg/kg for p.o.; from day 7 to 19) exerts dose-dependent antitumor effects manifested by the retardation of tumor growth[3].

Animal Model:BALB/c mice inoculated with C-26 cells[3]
Dosage:12.5, 25, 50 mg/kg for i.p.; 12.5, 50 mg/kg for p.o.
Administration:IP or PO; from day 7 to 19
Result:Exerted dose-dependent antitumor effects manifested by the retardation of tumor growth.
IC 50Human Endogenous Metabolite
PROTOPORPHYRINATO ZINC Preparation Products And Raw materials
Tag:PROTOPORPHYRINATO ZINC(15442-64-5) Related Product Information
Protoporphyrin IX 2,3,4,5-TETRAMETHYLPYRROLE Allylacetic acid ZINC NITRATE, TETRAHYDRATE 2,4-Dimethylpyrrole 2,5-Dimethyl-1H-pyrrole PROTOPORPHYRINATO ZINC 4-HEXENOIC ACID 3-BUTEN-1-AMINE 6-Heptenoic acid 3-METHYL-2-BUTEN-1-AMINE 1,3,6-HEPTATRIENE N-PROPYLETHYLIDENEAMINE 3,4-DIMETHYLPYRROLE 5-METHYL-4-HEXENOIC ACID 2,4-OCTADIENE HEPTA-4,6-DIENOIC ACID 3-ETHYL-2-METHYL-2-PENTENE