Drug Information
Drug General Information | |||||
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Drug ID |
D0Y9RD
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Former ID |
DNC008613
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Drug Name |
H-Tyr-Pro-Ala-Phe-NH2
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Synonyms |
YPAF-NH2
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Indication | Discovery agent | Investigative | [529365] | ||
Structure |
Download2D MOL |
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Canonical SMILES |
CC(C(=O)NC(CC1=CC=CC=C1)C(=O)N)NC(=O)C2CCCN2C(=O)C(CC3=<br />CC=C(C=C3)O)N
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InChI |
1S/C26H33N5O5/c1-16(24(34)30-21(23(28)33)15-17-6-3-2-4-7-17)29-25(35)22-8-5-13-31(22)26(36)20(27)14-18-9-11-19(32)12-10-18/h2-4,6-7,9-12,16,20-22,32H,5,8,13-15,27H2,1H3,(H2,28,33)(H,29,35)(H,30,34)/t16-,20-,21-,22-/m0/s1
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InChIKey |
RZZXLHCBXYDTOF-KPQYALRZSA-N
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Target and Pathway | |||||
Target(s) | Mu-type opioid receptor | Target Info | Inhibitor | [529365] | |
Substance-P receptor | Target Info | Inhibitor | [530745] | ||
NetPath Pathway | TCR Signaling Pathway | ||||
Pathway Interaction Database | IL4-mediated signaling events | ||||
References | |||||
Ref 529365 | Bioorg Med Chem. 2008 Apr 15;16(8):4341-6. Epub 2008 Mar 4.Internalisation of the mu-opioid receptor by endomorphin-1 and leu-enkephalin is dependant on aromatic amino acid residues. | ||||
Ref 530745 | J Med Chem. 2010 Mar 25;53(6):2383-9.Discovery of dipeptides with high affinity to the specific binding site for substance P1-7. |
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