E5757
Methionine Enkephalin-Arg-Phe acetate salt hydrate
≥97% (HPLC)
别名:
MERF, Tyr-Gly-Gly-Phe-Met-Arg-Phe
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关于此项目
经验公式（希尔记法）:
C42H56N10O9S · xC2H4O2 · yH2O
分子量:
877.02 (anhydrous free base basis)
NACRES:
NA.32
PubChem Substance ID:
UNSPSC Code:
12352209
MDL number:
Assay:
≥97% (HPLC)
assay
≥97% (HPLC)
storage temp.
−20°C
SMILES string
O.CC(O)=O.CSCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)Cc2ccc(O)cc2)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc3ccccc3)C(O)=O
InChI
1S/C42H56N10O9S.C2H4O2.H2O/c1-62-20-18-32(39(58)50-31(13-8-19-46-42(44)45)38(57)52-34(41(60)61)23-27-11-6-3-7-12-27)51-40(59)33(22-26-9-4-2-5-10-26)49-36(55)25-47-35(54)24-48-37(56)30(43)21-28-14-16-29(53)17-15-28;1-2(3)4;/h2-7,9-12,14-17,30-34,53H,8,13,18-25,43H2,1H3,(H,47,54)(H,48,56)(H,49,55)(H,50,58)(H,51,59)(H,52,57)(H,60,61)(H4,44,45,46);1H3,(H,3,4);1H2/t30-,31-,32-,33-,34-;;/m0../s1
InChI key
WOWLRTTTXHINBL-AVEXNAMASA-N
Biochem/physiol Actions
Endogenous opioid heptapeptide that is an agonist at μ, δ, and κ receptors; also binds to σ2 receptors.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Charlotte R Feddersen et al.
BMC genomics, 20(1), 497-497 (2019-06-19)
The introduction of genome-wide shRNA and CRISPR libraries has facilitated cell-based screens to identify loss-of-function mutations associated with a phenotype of interest. Approaches to perform analogous gain-of-function screens are less common, although some reports have utilized arrayed viral expression libraries
David L Phillips et al.
Cornea, 34(11), 1383-1386 (2015-09-24)
To evaluate the outcome of the Boston type 1 keratoprosthesis (KPro-1) in eyes with iridocorneal endothelial syndromes and failed keratoplasties. A retrospective review was performed of every eye with a history of iridocorneal endothelial syndrome and a failed corneal transplant
Peter Densen et al.
Journal of immunology (Baltimore, Md. : 1950), 205(6), 1535-1539 (2020-08-10)
C8α-γ deficiency was examined in four unrelated African Americans. Two individuals were compound heterozygotes for a previously reported point mutation in exon 9. mRNA from the remaining six C8A alleles contained a 10 nt insertion between nt 992 and 993