ChemicalBook--->CAS DataBase List--->23103-35-7

23103-35-7

23103-35-7 Structure

23103-35-7 Structure
IdentificationBack Directory
[Name]

Myo-Inositol Trispyrophosphate HexasodiuM Salt
[CAS]

23103-35-7
[Synonyms]

ITPP
ITTP HexasodiuM Salt
Myo-Inositol Tripyrphosphate HexasodiuM salt
Myo-Inositol Trispyrophosphate HexasodiuM Salt
Myo-Inositol Trispyrophosphate HexasodiuM Salt 9
MYO-INOSITOL TRISPYROPHOSPHATE HEXASODIUM (ITPP)
Inositol cyclic-1,2:3,4:5,6-tris(P,P'-dihydrogen diphosphate) hexasodium salt
Myo-Inositol Cyclic 1,2:3,4:5,6-Tris(dihydrogen pyrophosphate)) HexasodiuM Salt
Myo-Inositol Cyclic 1,2:3,4:5,6-Tris(P,P'-dihydrogen diphosphate) HexasodiuM Salt
[Molecular Formula]

C6H6Na6O21P6
[MDL Number]

MFCD28899029
[MOL File]

23103-35-7.mol
[Molecular Weight]

791.926
Chemical PropertiesBack Directory
[Melting point ]

>270°C (dec.)
[storage temp. ]

Hygroscopic, -20°C Freezer, Under Inert Atmosphere
[solubility ]

Water (Slightly, Sonicated)
[form ]

Solid
[color ]

White to Off-White
[Stability:]

Hygroscopic
Hazard InformationBack Directory
[Chemical Properties]

Off-White Solid
[Uses]

A novel membrane-permeant allosteric effector of hemoglobin (Hb), enhances the regulated oxygen release capacity of red blood cells, thus counteracting the effects of hypoxia in diseases such as cancer and cardiovascular ailments.
[in vivo]

Non-salt dose:
myo-Inositol trispyrophosphate (1.5 g/kg; intraperitoneal injection; twice a week for 4 weeks) has a protective effect in rat model of myocardial infarction[1].
myo-Inositol trispyrophosphate (1.5 g/kg; intravenous injection; once a week for 11 weeks) has antitumor activity in a rat model of pancreatic cancer[2].

Animal Model:Male Wistar rats (280-320 g) with myocardial infarction[1]
Dosage:1.5 g/kg (Non-salt dose)
Administration:Intraperitoneal injection (i.p.); twice a week for 4 weeks
Result:Essentially halted the increase of LV dilation and significantly reduced impairment of LV ejection fraction, while it had no effect on sham-operated rats.
Animal Model:DSL-6A/C1 tumors treated immunocompetent male Lewis rats[2]
Dosage:1.5 g/kg (Non-salt dose)
Administration:Intravenous injection (i.v.); once a week for 11 weeks
Result:Significantly extended the survival time of rats.
Basically did not cause liver metastasis and primary tumor growth was restricted to 2 cm3.
Restored the pO2 pressure in tumors reducing hypoxia-inducible and proangiogenic factors.
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