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
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
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was also studied in heart transplant recipients and in obesity patients, but these studies were terminated or withdrawn for different reasons.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
Title | Date | PubMed |
---|---|---|
Effects of prostacyclin on cardiovascular reflexes from the ventricular epicardium of the dog: comparison with the effects of prostaglandin E2. | 1981 Jun |
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Kappa- and delta-opioids block sympathetically dependent hyperalgesia. | 1991 Apr |
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Bradykinin-induced activation of nociceptors: receptor and mechanistic studies on the neonatal rat spinal cord-tail preparation in vitro. | 1992 Dec |
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S14080, a peripheral analgesic acting by release of an endogenous circulating opioid-like substance. | 1995 Jan |
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The agonist selectivity of a mouse B1 bradykinin receptor differs from human and rabbit B1 receptors. | 1996 Jun |
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Pharmacological modulation of secondary mediator systems--cyclic AMP and cyclic GMP--on inflammatory hyperalgesia. | 1999 Jun |
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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 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:01:32 GMT 2023
by
admin
on
Sat Dec 16 10:01:32 GMT 2023
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Record UNII |
6XS68K58Z5
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Record Status |
Validated (UNII)
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Record Version |
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6XS68K58Z5
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5979-11-3
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12358884
Created by
admin on Sat Dec 16 10:01:32 GMT 2023 , Edited by admin on Sat Dec 16 10:01:32 GMT 2023
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PARENT -> SALT/SOLVATE |
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ACTIVE MOIETY |