87734-77-8

Basic information

• Product Name: phyllolitorin
• Synonyms: L-Methioninamide,5-oxo-L-prolyl-L-leucyl-L-tryptophyl-L-alanyl-L-valylglycyl-L-seryl-L-phenylalanyl-;Ranatensin,2-L-leucine-3-de-L-proline-4-de-L-glutamine-9-L-serine-
• CAS NO: 87734-77-8
• Molecular Formula: C49H69N11O11S
• Molecular Weight: 1020.22
• Mol File: 87734-77-8.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 1514 °C at 760 mmHg
• Flash Point: 869.4 °C
• Appearance: /
• Density: 1.289 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.593
• CAS DataBase Reference: phyllolitorin(CAS DataBase Reference)
• NIST Chemistry Reference: phyllolitorin(87734-77-8)
• EPA Substance Registry System: phyllolitorin(87734-77-8)

Safety Data

• Hazardous Substances Data: 87734-77-8(Hazardous Substances Data)

Usage

Description

Phyllolitorin is a natural compound found in the plant Phyllanthus niruri, also known as stonebreaker or chanca piedra. It is a potent inhibitor of hepatitis B virus replication and possesses anti-inflammatory and antioxidant properties.

Uses

Used in Antiviral Applications:
Phyllolitorin is used as an antiviral agent for its ability to inhibit hepatitis B virus replication, making it a potential candidate for the development of new antiviral drugs.
Used in Liver Disorders Treatment:
Phyllolitorin is used as a therapeutic agent for liver disorders due to its anti-inflammatory and antioxidant properties, which may contribute to its traditional use in treating such conditions.
Used in Kidney Stone Treatment:
Phyllolitorin is used as a treatment for kidney stones, likely due to its traditional use and potential therapeutic effects.
Used in Urinary Tract Infections Treatment:
Phyllolitorin is used as a treatment for urinary tract infections, possibly due to its anti-inflammatory and antioxidant properties, as well as its traditional use in addressing such conditions.
Used in Natural Product Drug Discovery:
Phyllolitorin is used as a target for further research in the field of natural product drug discovery, given its ability to inhibit viral replication and its potential therapeutic effects.

InChI:InChI=1/C49H69N11O11S/c1-26(2)20-35(57-44(66)34-16-17-39(62)54-34)46(68)59-37(22-30-23-51-32-15-11-10-14-31(30)32)45(67)53-28(5)43(65)60-41(27(3)4)49(71)52-24-40(63)55-38(25-61)48(70)58-36(21-29-12-8-7-9-13-29)47(69)56-33(42(50)64)18-19-72-6/h7-15,23,26-28,33-38,41,51,61H,16-22,24-25H2,1-6H3,(H2,50,64)(H,52,71)(H,53,67)(H,54,62)(H,55,63)(H,56,69)(H,57,66)(H,58,70)(H,59,68)(H,60,65)/t28-,33-,34-,35-,36-,37-,38-,41-/m0/s1