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| CAS No.: | 52434-75-0 |
|---|---|
| Name: | LHRH (1-5) |
| Article Data: | 3 |
| Molecular Structure: | |
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| Formula: | C34H38 N8 O9 |
| Molecular Weight: | 702.724 |
| Synonyms: | L-Tyrosine,N-[N-[N-[N-(5-oxo-L-prolyl)-L-histidyl]-L-tryptophyl]-L-seryl]- |
| PSA: | 267.73000 |
| LogP: | 0.81160 |
- 81281-59-67-Benzylideneaminotheophylline
- 82993-81-5D-threo-Ritalinic acid hydrochloride
- 73441-42-6METHYL-5-CHLORO-2,2-DIMETHYLVALERATE
- 68439-39-4Poly(oxy-1,2-ethanediyl), alpha-(2-ethylhexyl)-omega-hydroxy-,
- 852475-26-4MC1568
- 958254-66-51H-Imidazo[4,5-b]pyridine-2-carboxaldehyde, 1-methyl-, hydrochloride
- 99170-93-1N-Methyl-2-oxazolamine
- 717878-06-31-(4-fluorophenyl)-4-nitro-1H-imidazole
- 914458-26-7[5-(2-fluorophenyl)-1-pentyl-1H-pyrrol-3-yl]-1-naphthalenyl-Methanone
- 548773-13-32-amino-4,6-dimethylpyrimidine-5-carboxylic acid
- 142822-22-8
L-pyroglutamyl-L-histidyl-L-trypthophyl-L-seryl-L-tyrosine tert-butyl ester
- 52434-75-0
pGlu-His-Trp-Ser-Tyr
| Conditions | Yield |
|---|---|
| With methoxybenzene; trifluoroacetic acid at 0℃; for 3h; |
- 2130-96-3
O-benzyl-N-tert-butoxycarbonyl-L-tyrosine
- 23680-31-1
BOC-O-benzyl-L-serine
- 13139-14-5
Boc-Trp-OH
- 25024-53-7
Boc-His(Dnp)-OH
- 52434-75-0
pGlu-His-Trp-Ser-Tyr
| Conditions | Yield |
|---|---|
| Yield given. Multistep reaction; |
- 16874-12-7
Tyr(tBu)
- 52434-75-0
pGlu-His-Trp-Ser-Tyr
| Conditions | Yield |
|---|---|
| Multi-step reaction with 4 steps 1: 78 percent / dioxane / 5 h / papain, dithioerythritol in phosphate buffer, pH 9 2: deprotection 3: 67 percent / methanol; H2O / 16 h / Ambient temperature; papain, dithioerythritol, pH 8 4: TFA, anisole / 3 h / 0 °C View Scheme |
- 142822-21-7
L-seryl-L-tyrosine tert-butyl ester
- 52434-75-0
pGlu-His-Trp-Ser-Tyr
| Conditions | Yield |
|---|---|
| Multi-step reaction with 2 steps 1: 67 percent / methanol; H2O / 16 h / Ambient temperature; papain, dithioerythritol, pH 8 2: TFA, anisole / 3 h / 0 °C View Scheme |
- 142822-20-6
N-benzyloxycarbonyl-L-seryl-L-tyrosine tert-butyl ester
- 52434-75-0
pGlu-His-Trp-Ser-Tyr
| Conditions | Yield |
|---|---|
| Multi-step reaction with 3 steps 1: deprotection 2: 67 percent / methanol; H2O / 16 h / Ambient temperature; papain, dithioerythritol, pH 8 3: TFA, anisole / 3 h / 0 °C View Scheme |
- 25575-88-6
L-Pyroglutamyl-L-histidine Methyl Ester
- 52434-75-0
pGlu-His-Trp-Ser-Tyr
| Conditions | Yield |
|---|---|
| Multi-step reaction with 3 steps 1: 75 percent / CH2Cl2; H2O / 16 h / Ambient temperature; α-chymotrypsin 2: 67 percent / methanol; H2O / 16 h / Ambient temperature; papain, dithioerythritol, pH 8 3: TFA, anisole / 3 h / 0 °C View Scheme |
- 20696-57-5
L-tryptophanamide
- 52434-75-0
pGlu-His-Trp-Ser-Tyr
| Conditions | Yield |
|---|---|
| Multi-step reaction with 3 steps 1: 75 percent / CH2Cl2; H2O / 16 h / Ambient temperature; α-chymotrypsin 2: 67 percent / methanol; H2O / 16 h / Ambient temperature; papain, dithioerythritol, pH 8 3: TFA, anisole / 3 h / 0 °C View Scheme |
- 33217-51-5
L-pyroglutamyl-L-histidine-L-tryptophane amide
- 52434-75-0
pGlu-His-Trp-Ser-Tyr
| Conditions | Yield |
|---|---|
| Multi-step reaction with 2 steps 1: 67 percent / methanol; H2O / 16 h / Ambient temperature; papain, dithioerythritol, pH 8 2: TFA, anisole / 3 h / 0 °C View Scheme |
- 67-56-1
methanol
- 52434-75-0
pGlu-His-Trp-Ser-Tyr
- 51871-39-7
L-pyroglutamyl-L-histidyl-L-tryptophyl-L-seryl-L-tyrosine methyl ester
| Conditions | Yield |
|---|---|
| With boron trifluoride at 0℃; for 8h; | 83% |
- 52434-75-0
pGlu-His-Trp-Ser-Tyr
- 207744-20-5
(S)-2-{(S)-3-Hydroxy-2-[(Z)-2-{(S)-3-(1H-imidazol-4-yl)-2-[((S)-5-oxo-pyrrolidine-2-carbonyl)-amino]-propionylamino}-3-(1H-indol-3-yl)-acryloylamino]-propionylamino}-3-(4-hydroxy-phenyl)-propionic acid
| Conditions | Yield |
|---|---|
| With (S)-tryptophan 2',3'-oxidase from Chromobacterium violaceum (ATCC 12472) In various solvent(s) at 30℃; for 20h; | 66% |
- Total:13 Page 1 of 1 1
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