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About This Item
Empirical Formula (Hill Notation):
C20H21ClN5O8PS
CAS Number:
Molecular Weight:
557.90
UNSPSC Code:
12352200
NACRES:
NA.77
MDL number:
InChI
1S/C20H21ClN5O8PS/c1-10(27)30-9-32-35(28)31-7-13-15(34-35)16(29-2)19(33-13)26-18-14(17(22)23-8-24-18)25-20(26)36-12-5-3-11(21)4-6-12/h3-6,8,13,15-16,19H,7,9H2,1-2H3,(H2,22,23,24)/t13-,15-,16-,19-,35?/m1/s1
SMILES string
NC1=NC=NC2=C1N=C(N2[C@H](O[C@H](CO3)[C@H]4OP3(OCOC(C)=O)=O)[C@@H]4OC)SC5=CC=C(C=C5)Cl
InChI key
FZMWUFYPEVDWPA-SILPBKOMSA-N
assay
≥98% (HPLC)
form
film or powder
color
colorless to light yellow
storage temp.
−20°C
Quality Level
Biochem/physiol Actions
8-pCPT-2′-O-Me-cAMP-AM (CPT-AM) is a membrane-permeant acetoxymethyl (AM) ester precusor form of the EPAC-selective cAMP analog (ESCA) 8-pCPT-2′-O-Me-cAMP (CPT). CPT-AM is >100-times more cell-permeable than CPT (by FRET using CFP-Epac-YFP-expressing A431; No effect by PKA FRET assay) and >100-times more efficient in stimulating cellular Rap1 activation (ECmax = 0.1 μM/CPT-AM vs. 100 μM/CPT; HUVECs).
Acetoxymethyl (AM) ester precusor of the EPAC-selective cAMP analog 8-pCPT-2′-O-Me-cAMP with greatly improved membrane permeability and cellular efficacy.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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