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BRADYKININ

CAS No.
58-82-2
Chemical Name:
BRADYKININ
Synonyms
bk;brs640;prs640;C00306;RPPGFSPFR;BRADYZIDE;Callideic;KallidinⅠ;BRADYKININ;Callidin I
CBNumber:
CB2141633
Molecular Formula:
C50H73N15O11
Molecular Weight:
1060.21
MDL Number:
MFCD00076258
MOL File:
58-82-2.mol
MSDS File:
SDS
Last updated:2024-03-27 11:49:37

BRADYKININ Properties

Melting point 170°C (rough estimate)
Boiling point 811.85°C (rough estimate)
alpha D25 -76.5° (c = 1.37 in 1N acetic acid)
Density 1.1171 (rough estimate)
refractive index 1.6930 (estimate)
RTECS EE1530000
storage temp. −20°C
solubility H2O: >40 mg/mL
pka 3.34±0.10(Predicted)
form White to off-white lyophilized solid
color Lyophilized powder
Water Solubility Soluble to 1 mg/ml in water.
Sequence H-Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg-OH
CAS DataBase Reference 58-82-2
FDA UNII S8TIM42R2W

SAFETY

Risk and Safety Statements

Safety Statements  22-24/25
WGK Germany  3
3-10-23

BRADYKININ price More Price(17)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich L9133 Leucine Enkephalin acetate salt hydrate ≥95% (HPLC) 58-82-2 10mg $112 2024-03-01 Buy
Sigma-Aldrich 05-23-0500 Bradykinin - CAS 58-82-2 - Calbiochem Induces the release of nitric oxide. 58-82-2 1mg $26.9 2024-03-01 Buy
Sigma-Aldrich L9133 Leucine Enkephalin acetate salt hydrate ≥95% (HPLC) 58-82-2 25mg $282 2024-03-01 Buy
Sigma-Aldrich 05-23-0500 Bradykinin - CAS 58-82-2 - Calbiochem Induces the release of nitric oxide. 58-82-2 5mg $82.8 2024-03-01 Buy
Sigma-Aldrich 05-23-0500 Bradykinin - CAS 58-82-2 - Calbiochem Induces the release of nitric oxide. 58-82-2 25mg $208 2024-03-01 Buy
Product number Packaging Price Buy
L9133 10mg $112 Buy
05-23-0500 1mg $26.9 Buy
L9133 25mg $282 Buy
05-23-0500 5mg $82.8 Buy
05-23-0500 25mg $208 Buy

BRADYKININ Chemical Properties,Uses,Production

Receptors

BKs signal via two GPCRs known as the B1 (BDKRB1) and B2 (BDKRB2) receptors. These BK receptor genes were the result of tandem duplication that predated the teleost tetraploidization while no extra copy was found in teleosts. B2 is constitutively expressed and predominant in different tissues while B1 expression is induced by inflammation. B1 expression in inflammatory tissues such as a wound area and vascular injury contributes to the inflammatory edema by its vasodilatory effect on local blood vessels. B2 is ubiquitously expressed in different tissues. In the aorta and large muscular arteries, including the carotid and mesenteric arteries, B2 is localized predominantly in the endothelium. However, in small arterioles toward the urinary bladder, myometrium, breast, etc., B2 is located predominantly in the smooth muscle rather than the endothelium. bdkrb2- overexpressed zebrafish induce IP3 accumulation by BK with an EC50 of 6.6 nM.

Signal transduction pathway

Both B1 and B2 trigger a typical Ca signaling of GPCRs. Receptor activation leads to phospholipase C (PLC) activation, intracellular Ca mobilization, release of endothelium-dependent relaxation factor (EDRF), and activation of PKC and cytosolic PLA2 that results in the release of prostaglandins (PGs). The endothelial nitric oxide synthase (eNOS) is also stimulated by B2 activation, leading to an increase in NO, stimulation of guanylyl cyclase, and an increase in cGMP. Most of these factors are EDRFs and are contributing to the hypotensive effect of BK. However, in smooth muscle cells, B2 activation activates PLC directly, leading to a transient increase in Ca2+ flux to induce muscle contraction. Although BK mostly induces vasorelaxation via endothelium-dependent signalings, in small arterioles where B2 is predominately localized in the smooth muscle cells, BK induces vasoconstriction. In the light of this dual function, [Arg0 ]-BK injection in teleosts was a vasopressor and could be related to a direct stimulation of B2 on smooth muscles, as the endothelium-dependent relaxing system is not prominent in teleosts.
Signal transduction pathway

Agonists and Antagonists

[Lys0 , des-Arg9 ]-BK is used as a B1 receptor agonist. Cereport (RMP-7) is a selective B2 agonist, and has been shown to transiently increase the permeability of the blood-brain barrier. The B1 antagonist BI-113823 possesses an antiinflammatory function. Icatibant (HOE 140 or JE 049) is a potent, specific, and selective peptidomimetic B2 antagonist.

Chemical Properties

Amorphous solid.

Uses

Leucine Enkephalin acetate salt hydrate has been used in the calibration of the Q-Tof Micro hybrid, triple quadrupole-orthogonal acceleration time of flight (TOF) instrument in single-stage TOF mode. It has also been used to perform the calibration of mass spectrometry. It has also been used in liquid chromatography-mass spectrometry (LCMS)/MS for calibration of the system and for relative correction of the spectra.

Uses

Bradykinin is used to lower blood pressure, increase bradykinin (by inhibiting its degradation) further lowering blood pressure. Bradykinin dilates blood vessels via the release of prostacyclin, nitric oxide, and endothelium-derived hyperpolarizing factor.

Definition

ChEBI: A linear nonapeptide messenger belonging to the kinin group of proteins, with amino acid sequence RPPGFSPFR. Enzymatically produced from kallidin in the blood, it is a powerful vasodilator that causes smooth muscle contraction, and may mediate inflammation

Biological Functions

The kallikrein–kinin system is an enzymatic pathway giving rise to two predominant vasoactive peptides, kallidin and bradykinin. Kallikrein, the enzyme responsible for the formation of these peptides, exists in plasma and tissues. However, circulating levels of the end products, kallidin and bradykinin, are quite low because the kallikrein enzymes are present largely in inactive forms. In addition, the short half-life of these peptides (15 seconds) also contributes to low plasma levels. In general, the kinins produce relaxation of vascular smooth muscle and vasodilation. Bradykinin causes vascular smooth muscle relaxation by stimulating the endothelium to release prostacyclin and nitric oxide. Blood flow to the brain, heart, viscera, skeletal muscle, and glands is increased. In nonvascular smooth muscle, bradykinin will produce a contractile response.
Other actions of kinins include activation of clotting factors simultaneously with the production of bradykinin. In the kidney, bradykinin production results in an increase in renal papillary blood flow, with a secondary inhibition of sodium reabsorption in the distal tubule. In the peripheral nervous system, bradykinin is important for the initiation of pain signals. It is also associated with the edema, erythema, and fever of inflammation.
Bradykinin exerts its physiological effects via two receptors, the B1 and B2 receptors, with most of its physiological effects being mediated by the B2 receptor. The precise function of the B1 receptor is unclear; however, some of the chronic inflammatory responses to bradykinin may be mediated through actions at this receptor.
Bradykinin antagonists of the B2 receptor are currently in development and may find utility in the treatment of pain associated with burns and such chronic inflammatory disorders as arthritis, asthma, and chronic pain.

General Description

Induces the release of nitric oxide. Other physiological functions include stimulation of pain receptors, inhibition of cAMP accumulation, induction of smooth muscle contraction, and vasodilation. Also involved in edema resulting from trauma or injury. Improves post-ischemic recovery of heart via a nitric oxide-dependent mechanism.

Hazard

Powerful vasodilator; increased capillary permeability; stimulates pain receptors; contraction of smooth muscle; teratogen; mutagenic.

Biochem/physiol Actions

Product does not compete with ATP.

Clinical Use

9-peptide, produced in response to tissue damage, inflammation, viral infections, etc. Produces pain, increased vascular permeability, and synthesis of prostaglandins.

storage

-20°C

BRADYKININ Preparation Products And Raw materials

Raw materials

Preparation Products

BRADYKININ Suppliers

Global( 88)Suppliers
Supplier Tel Email Country ProdList Advantage
Shenzhen Nexconn Pharmatechs Ltd
+86-755-89396905 +86-15013857715 admin@nexconn.com China 10248 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
BOC Sciences
+16314854226 inquiry@bocsci.com United States 19743 58
Hangzhou Go Top Peptide Biotech
0571-88211921 sales1@gotopbio.com CHINA 2609 58
Henan Alfa Chemical Co., Ltd
+8618339805032 alfa4@alfachem.cn China 12755 58
Zhejiang Hangyu API Co., Ltd
+8617531972939 anna@api-made.com China 2944 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 57511 58
Aoxuan Biological Technology Co., Ltd. 17073140108 CHINA 144 55
3B Pharmachem (Wuhan) International Co.,Ltd. 821-50328103-801 18930552037 3bsc@sina.com China 15848 69
GL Biochem (Shanghai) Ltd 21-61263452 13641803416 ymbetter@glbiochem.com China 9981 64

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View Lastest Price from BRADYKININ manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
BRADYKININ pictures 2019-12-23 BRADYKININ
58-82-2
US $1.00 / KG 1KG 99% 100KG Career Henan Chemical Co
  • BRADYKININ pictures
  • BRADYKININ
    58-82-2
  • US $1.00 / KG
  • 99%
  • Career Henan Chemical Co
RPPGFSPFR BRADYKININ BRADYKININ, TYROSYL BRADYKININ, LYSYL BRADYKININ, METHIONYL-LYSYL BRADYKININ, HUMAN BRADYKININ (HUMAN, BOVINE, RAT, MOUSE) ARG-PRO-PRO-GLY-PHE-SER-PRO-PHE-ARG H-ARG-PRO-PRO-GLY-PHE-SER-PRO-PHE-ARG-OH bk bradykinin(synthetic) brs640 prs640 BRADYZIDE Synthetic bradykinin Callidin I Kallidin 9 Kallidin I Callideic KallidinⅠ C00306 Leucine Enkephalin acetate salt hydrate Bradykinin - CAS 58-82-2 - Calbiochem Bradykinin, >98% Bradykinin Receptor,Bradykinin,Serine endopeptidases,inhibit,Threonine proteases,Inhibitor,Endogenous Metabolite,Serine proteases,Ser/Thr Protease 58-82-2 Bradykinins Biochemicals and Reagents BioChemical Amino Acids and Peptides Peptides peptide Chemical and pharmaceutical intermediates