ChemicalBook--->CAS DataBase List--->14325-05-4

14325-05-4

14325-05-4 Structure

14325-05-4 Structure
IdentificationBack Directory
[Name]

TIN PROTOPORPHYRIN IX DICHLORIDE
[CAS]

14325-05-4
[Synonyms]

SnPPIX
Nsc267099
TINPROTOPORPHYRIN
tin protoporphyrin IX
TIN PROTOPORPHYRIN IX DICHLORIDE
Tin Protoporphyrin IX (chloride)
Stannate(2-) dichloro[7,12-diethenyl-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropanoic acid]
[Molecular Formula]

C34H36Cl2N4O4Sn
[MDL Number]

MFCD00673909
[MOL File]

14325-05-4.mol
[Molecular Weight]

754.29
Chemical PropertiesBack Directory
[storage temp. ]

Store at RT
[solubility ]

Soluble to 25 mM in 1eq. NaOH and to 5 mM in DMSO
[form ]

Dark red to violet solid.
[color ]

Brown to reddish brown
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H315-H335
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
Hazard InformationBack Directory
[Uses]

Heme oxygenase (HO) converts protoheme to biliverdin, which in turn is enzymatically metabolized to bilirubin . While HO-2 is constitutively expressed, HO-1 can be induced by its heme substrate as well as by heavy metals, oxidizing agents, and other environmental stresses. TIN PROTOPORPHYRIN IX DICHLORIDE(SnPPIX) is a synthetic heme analog that selectively inhibits HO-1 (Ki = 11 nM) over HO-2 (IC50 = 7.5 μM). It also weakly inhibits endothelial nitric oxide synthase and soluble guanylyl cyclase (IC50s = 35 and 30 nM, respectively). SnPPIX prevents hyperbilirubinemia in neonates by blocking HO-1 activity that increases postnatally. It is rapidly cleared from plasma and persists in certain tissues, including kidney, liver, and spleen. SnPPIX is commonly used as a tool to study the role of HO-1 activity in cells and in animals.[Cayman Chemical]
[in vivo]

Tin protoporphyrin IX dichloride (intraperitoneal injection; 5 mg/kg; at 0, 7, 15, and 20 days) alone or combines with Gemcitabine significantly reduced the weight of pancreatic tumors (P < 0.05), decreases metastasis and improved the efficacy of Gemcitabine treatment[1].

Animal Model:Male and female athymic nude mice with PDAC cell-derived xenograft tumors[1]
Dosage:5 mg/kg
Administration:Intraperitoneal injection; at days 1, 4, 6, 8, 11, 13, 15, 18, and 20
Result:Inhibited tumor growth and sensitized tumors to chemotherapy (Gemcitabine).
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