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Merck
CN

D0569

DT-3 trifluoroacetate salt

≥95% (HPLC), lyophilized powder

Synonym(s):

Drosophila Antennapedia homeodomain (43-58)

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About This Item

Empirical Formula (Hill Notation):
C152H259N53O27S · xC2HF3O2
CAS Number:
Molecular Weight:
3293.09 (free base basis)
UNSPSC Code:
12352200
MDL number:
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assay

≥95% (HPLC)

form

lyophilized powder

composition

Peptide content, ~64%

color

white

shipped in

wet ice

storage temp.

−20°C

SMILES string

OC(=O)C(F)(F)F.CC[C@H](C)[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](N)CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc3ccccc3)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc4c[nH]c5ccccc45)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc6c[nH]cn6)C(N)=O

Biochem/physiol Actions

Cell permeable cGMP-dependent protein kinase type Ia (PKG) inhibitor


Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

新产品

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Thomas Krieg et al.
American journal of physiology. Heart and circulatory physiology, 288(4), H1976-H1981 (2004-12-14)
Bradykinin and acetylcholine (ACh) trigger preconditioning by ATP-sensitive K(+) (K(ATP)) channel-dependent production of reactive oxygen species (ROS). Recent evidence suggests that ROS production may in turn be influenced by cGMP-dependent protein kinase (PKG). This study utilized DT-2 and DT-3 peptides
Highly specific, membrane-permeant peptide blockers of cGMP-dependent protein kinase Ia inhibit NO-induced cerebral dilation
Dostmann, Wolfgang R.G. et al.
Proceedings of the National Academy of Sciences of the USA, 19, 14772 - 14777 (2000)
Wolfgang R G Dostmann et al.
Pharmacology & therapeutics, 93(2-3), 203-215 (2002-08-23)
The structural similarity of cyclic GMP-dependent protein kinase (cGPK) and cyclic AMP-dependent protein kinase (cAPK) has made it difficult to study cGPK pathways independent of those mediated by cAPK, primarily due to the lack of potent and selective cGPK inhibitors.