cas 2002-44-0, H-PRO-LEU-GLY-NH2 | Articles data ｜lookchem

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2002-44-0

Articles about 2002-44-0Total 8 be found

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PROCESS FOR LARGE SCALE LIQUID PHASE SYNTHESIS OF CARBETOCIN AND ITS NOVEL INTERMEDIATES
A process for large scale liquid phase synthesis of Carbetocin is disclosed. Novel intermediates of formula (A), formula (B), and processes for their preparation are also disclosed.
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(2017/11/06)

SYNTHESIS OF THE AMIDE OF THE C-TERMINAL TETRAPEPTIDE OF THE SEQUENCE OF OXYTOCIN
The synthesis has been effected of the amide of the tetrapeptide forming the sequence 6-9 of oxytocin with the use of benzyl protection of the thiol function of cysteine by two main schemes 1+3 and 2+2.The advantageousness of performing the synthesis by the 2+2 scheme has been shown.The overall yield of tetrapeptide using the method of condensation with the formation of mixed anhydrides amounted to 51percent by the scheme proposed.
Ivanov, A. K.,Antonov, A. A.,Donetskii, I. A.
p. 344 - 349
(2007/10/02)

BEHAVIORAL EFFECTS OF THYROLIBERIN, MELANOSTATIN, AND ITS ANALOGS
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Mazurov, A. A.,Andronati, S. A.,Lobasyuk, B. A.,Kabanov, V. M.,Korotenko, T. I.
p. 106 - 110
(2007/10/02)

Peptide syntheses with the N-PChd protective group. Synthesis of the hydrophobic segment 14-20 L-Ala-Leu-Ile-Leu-Leu-Ala-Gln of human lymphoblastoid interferon
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Khalifa,Jung,Rieker
p. 1068 - 1090
(2007/10/02)

Tumor-resolving and histolytic medicaments and their use
Dehydrooligopeptides, some of which are known, demonstrate histolytic and tumor-resolving activity and may be used in medicaments causing the lysis of animal tissues and/or tumors in warm-blooded animals.
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(2008/06/13)

DESIGN AND SYNTHESIS OF A MULTI-DETACHABLE BENZHYDRYLAMINE-RESIN FOR SOLID PHASE PEPTIDE SYNTHESIS
Peptides with C-terminal α-carboxamides were synthesized from a multi-detachable benzhydrylamine-resin containing a Boc-(4-acetoxy)benzhydrylamine handle of unambiguous origin.The peptides bound to the new resin are stable to trifluoroacetic acid, but are cleavable by hydrogen fluoride, base and nucleophiles to give unprotected or protected peptide fragments.
Tam, James P.,DiMarchi, Richard D.,Merrifield, R. B.
p. 2851 - 2854
(2007/10/02)

Eine elektrochemisch einfuehrbare Aminoschutzgruppe fuer die Peptidsynthese
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Khalifa, Mohamed Hassen,Jung, Guenther,Rieker, Anton
p. 739 - 740
(2007/10/02)

VALIDITY OF METHOXYCARBONYL AS AN N-PROTECTING GROUP IN PEPTIDE SYNTHESIS: NEW SYNTHESIS OF MSH-RELEASE INHIBITING FACTOR
N-Methoxycarbonyl (MOC)-amino acids regenerate the parent amino acids by treatment with dimethyl sulphide and methanesulphonic acid.Synthesis of MSH-Release Inhibiting Factor was accomplished using MOC-amino acids and applying the above mentioned deblocking method.
Irie, Hiroshi,Nakanishi, Hiromi,Fujii, Nobutaka,Mizuno, Yukio,Fushimi, Tamaki,et al.
p. 705 - 708
(2007/10/02)

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Chemical Properties

Melting Point: 122-123 °C(Solv: water (7732-18-5))
Boiling Point: 626.2 °C at 760 mmHg
Flash Point:332.5 °C
Density: 1.147 g/cm³
Solubility:≥59.1 mg/mL in DMSO; ≥50 mg/mL in EtOH; ≥50 mg/mL in H2O
Storage Temp.:-15°C
Vapor Pressure: 1.34E-15mmHg at 25°C
Refractive Index: 1.51
PKA: 14.10±0.20(Predicted)
PSA: 113.32000
LogP: 0.68170

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