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Details

Stereochemistry ABSOLUTE
Molecular Formula C50H73N15O11.3C2H4O2
Molecular Weight 1240.3644
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BRADYKININ TRIACETATE

SMILES

CC(O)=O.CC(O)=O.CC(O)=O.N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N2CCC[C@H]2C(=O)NCC(=O)N[C@@H](CC3=CC=CC=C3)C(=O)N[C@@H](CO)C(=O)N4CCC[C@H]4C(=O)N[C@@H](CC5=CC=CC=C5)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O

InChI

InChIKey=GGIQAOBCVDFMSP-XFUQBTSGSA-N
InChI=1S/C50H73N15O11.3C2H4O2/c51-32(16-7-21-56-49(52)53)45(72)65-25-11-20-39(65)47(74)64-24-9-18-37(64)43(70)58-28-40(67)59-34(26-30-12-3-1-4-13-30)41(68)62-36(29-66)46(73)63-23-10-19-38(63)44(71)61-35(27-31-14-5-2-6-15-31)42(69)60-33(48(75)76)17-8-22-57-50(54)55;3*1-2(3)4/h1-6,12-15,32-39,66H,7-11,16-29,51H2,(H,58,70)(H,59,67)(H,60,69)(H,61,71)(H,62,68)(H,75,76)(H4,52,53,56)(H4,54,55,57);3*1H3,(H,3,4)/t32-,33-,34-,35-,36-,37-,38-,39-;;;/m0.../s1

HIDE SMILES / InChI

Molecular Formula C50H73N15O11
Molecular Weight 1060.2085
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 8
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula C2H4O2
Molecular Weight 60.052
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Bradykinin, a pro-inflammatory mediator is also a neuromediator and regulator of several vascular and renal functions. Bradykinin can act as a vasoactive substance along with histamine in inflammation and swelling as it is a potent vasodilator. In addition, it triggers the release of other mediators such as nitric oxide in inflammatory and cancer tissues. Bradykinin acts via specific cell surface receptors: bradykinin receptor, B1 and B2 that are G-protein coupled receptors of the seven-transmembrane domain family. It was shown that increased plasma levels of bradykinin lead to the angioedema as the common major clinical manifestation. Bradykinin was also studied in heart transplant recipients and in obesity patients, but these studies were terminated or withdrawn for different reasons. Bradykinin is also an important growth factor for many cancers. Bradykinin antagonists showed higher potency than standard anti-cancer drugs, without evident toxicity to the hosts, that is why they have great promise for the development of new anti-cancer drugs.

Approval Year

PubMed

PubMed

TitleDatePubMed
Kappa- and delta-opioids block sympathetically dependent hyperalgesia.
1991 Apr
Bradykinin-induced activation of nociceptors: receptor and mechanistic studies on the neonatal rat spinal cord-tail preparation in vitro.
1992 Dec
Differential pharmacology of cloned human and mouse B2 bradykinin receptors.
1994 Jan
Bradykinin-induced sensitization of afferent neurons in the rat paw.
1994 Mar
Mechanisms for protective effects of free radical scavengers on gentamicin-mediated nephropathy in rats.
1994 Mar
BW373U86, a delta-opioid receptor agonist, reverses bradykinin-induced thermal allodynia in rhesus monkeys.
1995 Apr 24
S14080, a peripheral analgesic acting by release of an endogenous circulating opioid-like substance.
1995 Jan
Cytokine-mediated inflammatory hyperalgesia limited by interleukin-10.
1995 Jun
The agonist selectivity of a mouse B1 bradykinin receptor differs from human and rabbit B1 receptors.
1996 Jun
Stable expression of the human kinin B1 receptor in Chinese hamster ovary cells. Characterization of ligand binding and effector pathways.
1997 Apr 25
Novel subtype-selective nonpeptide bradykinin receptor antagonists FR167344 and FR173657.
1997 Feb
The nonpeptide B2 receptor antagonist FR173657: inhibition of effects of bradykinin related to its role in nociception.
1998 Jul
The involvement of K+ channels and Gi/o protein in the antinociceptive action of the gallic acid ethyl ester.
1999 Aug 20
Effects of mexiletine on algogenic mediator-induced nociceptive responses in mice.
1999 Jul-Aug
Molecular characterisation of cloned bradykinin B1 receptors from rat and human.
1999 Jun 25
Multiple antimicrobial peptides and peptides related to bradykinin and neuromedin N isolated from skin secretions of the pickerel frog, Rana palustris.
2000 Nov 30
S-Glutathiolation by peroxynitrite activates SERCA during arterial relaxation by nitric oxide.
2004 Nov
Enhancement of arachidonic acid signaling pathway by nicotinic acid receptor HM74A.
2006 Jun 23
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:01:32 UTC 2023
Edited
by admin
on Sat Dec 16 10:01:32 UTC 2023
Record UNII
6XS68K58Z5
Record Status Validated (UNII)
Record Version
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Name Type Language
BRADYKININ TRIACETATE
Common Name English
BRADYKININ TRIACETATE SALT
Common Name English
BRADYKININ ACETATE (1:3)
Common Name English
ARGININE, N2-(N-(1-(N-(N-(N-(1-(1-L-ARGINYL-L-PROLYL)-L-PROLYL)GLYCYL)-3-PHENYL-L-ALANYL)-L-SERYL)-L-PROLYL)-3-PHENYL-L-ALANYL)-, TRIACETATE
Systematic Name English
Code System Code Type Description
FDA UNII
6XS68K58Z5
Created by admin on Sat Dec 16 10:01:32 UTC 2023 , Edited by admin on Sat Dec 16 10:01:32 UTC 2023
PRIMARY
CAS
5979-11-3
Created by admin on Sat Dec 16 10:01:32 UTC 2023 , Edited by admin on Sat Dec 16 10:01:32 UTC 2023
PRIMARY
PUBCHEM
12358884
Created by admin on Sat Dec 16 10:01:32 UTC 2023 , Edited by admin on Sat Dec 16 10:01:32 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY