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Cholecystokinins
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Description
Biochem/physiol Actions
Product #
Boc-Trp-Met-Phe amide ≥97% (TLC)
B3144
Cholecystokinin (CCK) Fragment 26-33 Amide, Non-sulfated ≥95% (HPLC), powder
Biologically inactive form of CCK-8; CCK
B
/gastrin receptor agonist that has no activity at the CCK
A
receptor.
C2901
Cholecystokinin Fragment 30-33 Amide hydrochloride ≥95% (HPLC)
CCK
B
cholecystokinin receptor agonist; anxiogenic.
T6515
Cholecystokinin Precursor Fragment 107-115 Desulfated human >97% (HPLC)
Desulfated fragment of the cholecystokinin precursor protein.
C9482
Cholecystokinin-33, sulfated human ~85% (HPLC)
Cholecystokinin peptide hormone that has been found to be the most abundant form in human intestine and plasma. CCK-33 has equally potent satiating power as CCK-8. The tyrosine is sulfated, which is required for biological activity.
C2362
Lorglumide sodium salt solid
Potent and selective non-peptide cholecystokinin (CCK
A
) receptor antagonist; orally active.
L109
Pentagastrin ≥95% (HPLC), powder
CCK
B
agonist that stimulates gastric acid secretion; anxiogenic.
B1636
Proglumide sodium salt solid
CCK antagonist; selectively blocks CNS effects.
Non-peptide cholecystokinin receptor antagonist that has greater selectivity for the CCK
A
subtype; orally active.
M006
(Tyr[SO
3
H]
27
)Cholecystokinin fragment 26-33 Amide ≥97% (HPLC), powder
Neurotransmitter; predominant form of CCK in CNS and gastrointestinal tract; may play a role in satiety.
C2175
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