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Terlipressin Acetate

Terlipressin Acetate structure

Terlipressin Acetate 

structure

Description

Terlipressin acetate is a vasopressin analogue with potent vasoactive properties. Terlipressin acetate is a highly selective vasopressin V1 receptor agonist that reduces the splanchnic blood flow and portal pressure and controlling acute variceal bleeding. Terlipressin acetate exerts anti-inflammatory and anti-oxidative effects. Terlipressin acetate has the potential for hepatorenal syndrome and norepinephrine-resistant septic shock treatment[1][2][3][4][5].

Terlipressin Acetate Basic Attributes

1347.476

1346.538330

Computed Properties

Molecular Weight:1347.5
Hydrogen Bond Donor Count:18
Hydrogen Bond Acceptor Count:23
Rotatable Bond Count:25
Exact Mass:1346.53835680
Monoisotopic Mass:1346.53835680
Topological Polar Surface Area:638
Heavy Atom Count:93
Complexity:2410
Defined Atom Stereocenter Count:8
Covalently-Bonded Unit Count:3
Compound Is Canonicalized:Yes

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