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B1901

Sigma-Aldrich

Bradykinin Fragment 2-9

≥97% (HPLC)

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About This Item

Formula empirica (notazione di Hill):
C44H61N11O10
Numero CAS:
16875-11-9
Peso molecolare:
904.02
Numero MDL:
MFCD00076264
Codice UNSPSC:
12352200
ID PubChem:
24891619
NACRES:
NA.32

Livello qualitativo

200

Saggio

≥97% (HPLC)

Stato

powder

N° accesso UniProt

P01042

Temperatura di conservazione

−20°C

Stringa SMILE

NC(=N)NCCCC(NC(=O)C(Cc1ccccc1)NC(=O)C2CCCN2C(=O)C(CO)NC(=O)C(Cc3ccccc3)NC(=O)CNC(=O)C4CCCN4C(=O)C5CCCN5)C(O)=O

InChI

1S/C44H61N11O10/c45-44(46)48-20-8-16-30(43(64)65)51-38(59)32(24-28-13-5-2-6-14-28)52-40(61)35-18-10-22-55(35)42(63)33(26-56)53-37(58)31(23-27-11-3-1-4-12-27)50-36(57)25-49-39(60)34-17-9-21-54(34)41(62)29-15-7-19-47-29/h1-6,11-14,29-35,47,56H,7-10,15-26H2,(H,49,60)(H,50,57)(H,51,59)(H,52,61)(H,53,58)(H,64,65)(H4,45,46,48)
ZZHVXIPXTCBVBE-UHFFFAOYSA-N

Informazioni sul gene

human ... KNG1 (includes EG:3827)

Amino Acid Sequence

Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg

Azioni biochim/fisiol

Inhibits ACE (angiotensin converting enzyme) and potentiates bradykinin (BK).
The des-arginine-1 bradykinin (BK) peptide (2-9) has no detectable contractile activity, inhibits ACE (angiotensin converting enzyme) and potentiates BK.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
SLCH7367
SLCG4851
SLBX4891
SLBQ9782V
SLBB4763V

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Cristiano R Jesse et al.
Pharmacology, biochemistry, and behavior, 91(4), 573-580 (2008-10-22)
The objective of this study was to extend our previous findings by investigating in greater detail the mechanisms that might be involved in the antinociceptive action of p-methoxyl-diphenyl diselenide, (MeOPhSe)(2), in mice. The pretreatment with nitric oxide precursor, l-arginine (600
G S Bedi et al.
Biochimica et biophysica acta, 842(1), 90-99 (1985-09-27)
Four hybridoma cell lines have been established that secrete monoclonal antibodies to nonapeptide bradykinin. Bradykinin coupled to ovalbumin, using 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide as coupling agent, was used to immunize BALB/c mice. Spleen cells from the immunized animals were fused to P3-X63-AG8-653 mouse
Julia Laskin et al.
Journal of the American Chemical Society, 125(6), 1625-1632 (2003-02-06)
Time- and collision energy-resolved surface-induced dissociation (SID) of des-Arg(1)- and des-Arg(9)-bradykinin on a fluorinated self-assembled monolayer (SAM) surface was studied by use of a novel Fourier transform ion cyclotron resonance mass spectrometer (FT-ICR MS) specially equipped to perform SID experiments.
B W Busser et al.
The Journal of urology, 160(6 Pt 1), 2267-2273 (1998-11-17)
Bradykinin 1 (B1) receptors have been shown to be upregulated at sites of inflammation. The purpose of this study was to determine the effect of lipopolysaccharide (LPS) on B1 receptor modulation in the isolated mouse bladder. The contractile responses of
S Mohammed et al.
Journal of mass spectrometry : JMS, 36(12), 1260-1268 (2001-12-26)
A novel tandem quadrupole mass spectrometer is described that enables gaseous collision-induced dissociation (CID) and surface-induced dissociation (SID) experiments. The instrument consists of a commercially available triple quadrupole mass spectrometer connected to an SID region and an additional, orthogonal quadrupole
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