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Boc-L-Ala-L-Leu-L-Glu(OBzl)-L-Lys(ClZ)-OH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

237425-50-2

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237425-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 237425-50-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,7,4,2 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 237425-50:
(8*2)+(7*3)+(6*7)+(5*4)+(4*2)+(3*5)+(2*5)+(1*0)=132
132 % 10 = 2
So 237425-50-2 is a valid CAS Registry Number.

237425-50-2Relevant academic research and scientific papers

A 12-porphyrin system: Syntheses of peptide porphyrins with multiple histidines and the aggregation behavior in the presence of hemin

Ushiyama, Masato,Yoshino, Atsushi,Yamamura, Takeshi,Shida, Yasuo,Arisaka, Fumio

, p. 1351 - 1364 (2007/10/03)

We succeeded in combining multiple-histidine peptides with porphyrins; that is to say, we synthesized three peptide porphyrins consisting of α4- meso-tetrakis(o-aminophenyl)porphyrin, α4-H2TAPP, and amphiphilic peptide, α4(PepA18)(n)(AG)(4-n)-H2TAPP (n = 1, 3, and 4; PepA18 = EEALEKHEKALEKHEKAG), in the liquid phase. These compounds were designed to construct multiple porphyrin systems; in other words, each peptide attached on the H2TAPP was designed to contain two histidines. The stability of the porphyrins, (AG)4-H2TAPP and (AG)1(Boc-AG)3-H2TAPP, as well as the coupling conditions between the porphyrin fragments and the 16-residue peptide, EEALEKHEKALEKHEK, to give α4-(PepA18)(n)(AG)(4-n)-H2TAPP (n = 1, 3, and 4) were studied in detail with respect to the temperature, solvents, coupling reagents, additives, and amines. This search revealed that the combination of DMF/benzotriazol-1-yl-oxytris(pyrrolidino)phosphonium hexafluorophosphate (PyBOP)/N,N-diisopropylethylamine is suitable for the purpose. The search also clarified that it is possible to synthesize α4- (PepA18)4-H2TAPP and α4-(PepA18)3(AG)1-H2TAPP selectively by choosing the coupling additives 1-hydroxy-7-azabenzotriazole (HOAt) and 1- hydroxybenzotriazole (HOBt, respectively. All of the compounds showed 40% helicity in a solution (phospate buffer, pH = 7.0) containing 2,2,2- trifluoroethanol (TFE). The UV-vis and circular-dichroism spectrophotometric titrations of Fe(III) protoporphyrin IX chloride, B, with α4(PepA18)4- ZnTAPP, A, indicated that up to three equivalents of B were incorporated into A in a buffer solution containing 15% TFE. Sedimentation-equilibrium ultracentrifugation experiments showed that A is a dimer in the solution, and that this dimer is transformed to a trimer when B is incorporated into A. These results suggest that A achieves a 12-porphyrin system consisting of different kinds of metalloporphyrin.

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