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B0507

Sigma-Aldrich

Bradykinin potentiator B

≥97% (TLC)

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About This Item

Empirical Formula (Hill Notation):
C56H91N15O13
CAS Number:
Molecular Weight:
1182.41
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

Assay

≥97% (TLC)

form

solid

mol wt

~_1.2 kDa

storage temp.

−20°C

SMILES string

CCC(C)C(NC(=O)C(CCCCN)NC(=O)C1CCCN1C(=O)C(CCCNC(N)=N)NC(=O)C2CCCN2C(=O)C3CCCN3C(=O)C(CC(C)C)NC(=O)CNC(=O)C4CCC(=O)N4)C(=O)N5CCCC5C(=O)N6CCCC6C(O)=O

InChI

1S/C56H91N15O13/c1-5-33(4)45(54(82)70-28-12-19-41(70)53(81)71-29-13-20-42(71)55(83)84)66-47(75)34(14-6-7-23-57)64-48(76)38-16-9-25-67(38)50(78)36(15-8-24-60-56(58)59)65-49(77)39-17-10-26-68(39)52(80)40-18-11-27-69(40)51(79)37(30-32(2)3)63-44(73)31-61-46(74)35-21-22-43(72)62-35/h32-42,45H,5-31,57H2,1-4H3,(H,61,74)(H,62,72)(H,63,73)(H,64,76)(H,65,77)(H,66,75)(H,83,84)(H4,58,59,60)

InChI key

JXGBFZMUUPNIBD-UHFFFAOYSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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E B Sabia et al.
Journal of medicinal chemistry, 20(12), 1679-1681 (1977-12-01)
The structural requirements for prolonged residual ("sensitizing") activity in bradykinin-potentiating peptides (BPP's) were investigated through a study of seven synthetic BPP's including three not previously described: [Lys6]-BPP9a, [Gly6]potentiator B, and [Lys6,Gln8]potentiator B. The quantitation of the sensitizing activities in the
Bradykinin-potentiating peptides from the venom of Agkistrodon halys blomhoffi. Isolation of five bradykinin potentiators and the amino acid sequences of two of them, potentiators B and C.
H Kato et al.
Biochemistry, 10(6), 972-980 (1971-03-16)
M Tominaga et al.
Journal of medicinal chemistry, 18(2), 130-133 (1975-02-01)
In a study of the relationship between structure and activity of bradykinin potentiating peptides (BPP), six analogs and homologs of peptides occurring in the venoms of Bothrops jararaca and Agkistrodon halys blomhoffii were synthesized and assayed in the isolated guinea

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