US2016008385A1PendingUtilityA1
Adrenomedullin production enhancer
Assignee: NAT UNIVERSITY CORP ASAHIKAWA MEDICAL COLLEGEPriority: Feb 19, 2008Filed: Sep 25, 2015Published: Jan 14, 2016
Est. expiryFeb 19, 2028(~1.6 yrs left)· nominal 20-yr term from priority
A61P 9/12A61P 9/00A61P 43/00A61P 29/00A61K 31/164A61K 36/258A61K 36/75A61P 15/00C07J 9/00C07J 17/005A61K 31/575A61K 36/9068A61P 11/00A61P 19/00A61P 1/16A61K 31/704A61P 13/00A61P 1/00A61K 31/12A61P 1/04
40
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
It is an object of the invention to discover a substance that effectively increases the production of adrenomedullin, as well as to provide an adrenomedullin production-enhancing agent utilizing this substance. The adrenomedullin production-enhancing agent is characterized by inclusion of a ginsenoside, a sanshool, and/or a shogaol as active ingredients.
Claims
exact text as granted — not AI-modified1 . A method of treating hepatitis in a subject in need thereof comprising, administering to the subject an effective amount of an agent comprising:
a compound represented by formula (1):
wherein R 1 , R 2 , and R 3 , which may be identical or different, each represent a hydrogen atom, a hydroxyl group, —O-Glc, —O-Glc-Glc, —O-Glc-Ara, or —O-Glc—Rha, wherein Glc represents a glucose residue, Ara represents an arabinose residue, and Rha represents a rhamnose residue; and
a compound represented by formula (2):
wherein R 4 represents a hydrogen atom or a hydroxyl group, m is 1 or 2, and a wavy bond line indicates either a Z- or E-configuration; and/or
a compound represented by formula (3):
wherein n is 4, 6, or 8.
2 . The method according to claim 1 , wherein the compound represented by formula (1) is at least one ginsenoside selected from the group consisting of ginsenoside Rb 1 , ginsenoside Rb 2 , ginsenoside Rc, ginsenoside Rd, ginseonside Re, ginsenoside Rg 1 , ginsenoside Rg 2 , and ginsenoside Rh 1 .
3 . The method agent according to claim 1 , wherein the compound represented by formula (2) is at least one sanshool selected from the group consisting of α-sanshool, β-sanshool, γ-sanshool, hydroxy-α-sanshool, hydroxy-β-sanshool, and hydroxy-γ-sanshool.
4 . The method according to claim 1 , wherein the compound represented by formula (3) is at least one compound selected from the group consisting of 6-shogaol, 8-shogaol, and 10-shogaol.
5 . A method of treating hepatitis in a subject in need thereof comprising, administering to the subject an effective amount of an agent comprising:
a crude drug comprising the compound represented by formula (1):
wherein R 1 , R 2 , and R 3 , which may be identical or different, each represent a hydrogen atom, a hydroxyl group, —O-Glc, —O-Glc-Glc, —O-Glc-Ara, or —O-Glc-Rha, wherein Glc represents a glucose residue, Ara represents an arabinose residue, and Rha represents a rhamnose residue; and
a crude drug comprising the compound represented by formula (2):
wherein R 4 represents a hydrogen atom or a hydroxyl group, m is 1 or 2, and a wavy bond line indicates either a Z- or E-configuration; and/or
a crude drug comprising the compound represented by formula (3):
wherein n is 4, 6, or 8.
6 . The method according to claim 5 , wherein the crude drug comprising the compound represented by formula (1) is ginseng.
7 . The method according to claim 5 , wherein the crude drug comprising the compound represented by formula (2) is Japanese pepper.
8 . The method according to claim 5 , wherein the crude drug containing the compound represented by formula (3) is dried ginger rhizome.
9 . A method of treating hepatitis in a subject in need thereof comprising, administering to the subject an effective amount of an agent comprising: a Kampo medicine prescription comprising:
a crude drug comprising the compound represented by formula (1);
wherein R 1 , R 2 , and R 3 , which may be identical or different, each represent a hydrogen atom, a hydroxyl group, —O-Glc, —O-Glc-Glc, —O-Glc-Ara, or —O-Glc-Rha, wherein Glc represents a glucose residue, Ara represents an arabinose residue, and Rha represents a rhamnose residue; and
a crude drug comprising the compound represented by formula (2):
wherein R 4 represents a hydrogen atom or a hydroxyl group, m is 1 or 2, and a wavy bond line indicates either a Z- or E-configuration; and/or
a crude drug comprising the compound represented by formula (3):
wherein n is 4, 6, or 8.
10 . The method according to claim 9 , wherein the Kampo medicine prescription is Daikenchutou.
11 - 20 . (canceled)Join the waitlist — get patent alerts
Track US2016008385A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.