CAS 141801-26-5: Endomorphin-2
Formula:C32H37N5O5
InChI:InChI=1/C32H37N5O5/c33-25(18-23-13-15-24(38)16-14-23)32(42)37-17-7-12-28(37)31(41)36-27(20-22-10-5-2-6-11-22)30(40)35-26(29(34)39)19-21-8-3-1-4-9-21/h1-6,8-11,13-16,25-28,38H,7,12,17-20,33H2,(H2,34,39)(H,35,40)(H,36,41)/t25-,26-,27-,28-/m0/s1
SMILES:c1ccc(cc1)C[C@@H](C(=N)O)N=C([C@H](Cc1ccccc1)N=C([C@@H]1CCCN1C(=O)[C@H](Cc1ccc(cc1)O)N)O)O
Synonyms:- Endomorphin-2 (Human, Bovine)
- Ypff-Nh2
- Tyr-Pro-Phe-Phe-Nh2
- (2S)-1-[(2S)-2-amino-3-(4-hydroxyphenyl)propanoyl]-N-[(1S)-1-[[(1S)-1-carbamoyl-2-phenyl-ethyl]carbamoyl]-2-phenyl-ethyl]pyrrolidine-2-carboxamide
- L-tyrosyl-L-prolyl-L-phenylalanyl-L-phenylalaninamide
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Found 7 products.
L-Phenylalaninamide, L-tyrosyl-L-prolyl-L-phenylalanyl-
CAS:Formula:C32H37N5O5Purity:98%Color and Shape:SolidMolecular weight:571.6667Endomorphin-2 trifluoroacetate salt
CAS:Endomorphin-2 is a cyclic peptide that is the endogenous ligand for the neurokinin-1 receptor and kappa-opioid receptors. It has been shown to have analgesic, anti-inflammatory, and antidiarrheal properties. Endomorphin-2 also has been shown to inhibit platelet aggregation and vasoconstriction in vivo. The biological activities of endomorphin-2 are similar to those of endomorphin-1, but it differs structurally in that it contains a single intramolecular hydrogen bond between the amide nitrogen of Tyr and Pro. This intramolecular hydrogen bond may be responsible for the high potency of endomorphin-2, as well as its conformational stability.Formula:C32H37N5O5Purity:Min. 95%Molecular weight:571.67 g/molEndomorphin 2
CAS:EM-2 reduces sEPSC frequency/amplitude in lamina IX motoneurons; CTOP reverses this. EM-2-IR affects limb muscles via presynaptic/postsynaptic mechanisms.Formula:C32H37N5O5Purity:99.64%Color and Shape:SolidMolecular weight:571.67Endomorphin-2
CAS:Endomorphin-2 is a cyclic peptide that has been shown to have analgesic and anti-inflammatory effects. It binds to the kappa-opioid receptor and inhibits locomotion in mice. It also has shown to be effective at treating bowel disease in vivo models. The biological properties of endomorphin-2 include its ability to stimulate the release of neurokinin-1 from trigeminal nerve endings, which then stimulates the release of substance P from sensory neurons. Endomorphin-2 does not bind to receptors for endomorphin 1 or endomorphin 3, but it does bind with high affinity to the neurokinin-1 receptor.Formula:C32H37N5O5Purity:Min. 95%Molecular weight:571.67 g/mol
