Cas 1190989-79-7,cyclo(-L/D-Phg-Arg-Arg-Nal-Gly-); L/D-Phg = L/D-phenylglycyl, Nal = L-3-(2-naphthyl)alanyl

1190989-79-7

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Basic information

Product Name: cyclo(-L/D-Phg-Arg-Arg-Nal-Gly-); L/D-Phg = L/D-phenylglycyl, Nal = L-3-(2-naphthyl)alanyl
Synonyms:
CAS NO:1190989-79-7
Molecular Formula:
Molecular Weight: 699.813
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: cyclo(-L/D-Phg-Arg-Arg-Nal-Gly-); L/D-Phg = L/D-phenylglycyl, Nal = L-3-(2-naphthyl)alanyl(CAS DataBase Reference)
NIST Chemistry Reference: cyclo(-L/D-Phg-Arg-Arg-Nal-Gly-); L/D-Phg = L/D-phenylglycyl, Nal = L-3-(2-naphthyl)alanyl(1190989-79-7)
EPA Substance Registry System: cyclo(-L/D-Phg-Arg-Arg-Nal-Gly-); L/D-Phg = L/D-phenylglycyl, Nal = L-3-(2-naphthyl)alanyl(1190989-79-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1190989-79-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1190989-79-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,9,8 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1190989-79:
(9*1)+(8*1)+(7*9)+(6*0)+(5*9)+(4*8)+(3*9)+(2*7)+(1*9)=207
207 % 10 = 7
So 1190989-79-7 is a valid CAS Registry Number.

1190989-79-7Upstream product

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1190989-79-7Relevant academic research and scientific papers

Structure-activity relationship study on artificial CXCR4 ligands possessing the cyclic pentapeptide scaffold: The exploration of amino acid residues of pentapeptides by substitutions of several aromatic amino acids

Tanaka, Tomohiro,Nomura, Wataru,Narumi, Tetsuo,Esaka, Ai,Oishi, Shinya,Ohashi, Nami,Itotani, Kyoko,Evans, Barry J.,Wang, Zi-Xuan,Peiper, Stephen C.,Fujii, Nobutaka,Tamamura, Hirokazu

, p. 3805 - 3809 (2009)

Previously, downsizing of a 14-residue peptidic CXCR4 antagonist 1 has led to the development of a highly potent CXCR4 antagonist 2 [cyclo(-d-Tyr 1-Arg2-Arg3-Nal4-Gly5-)]. In the present study, cyclic

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