Bilaid B
AlkaPlorer ID: AK011592
Synonym: None
IUPAC Name: (2R)-2-[[(2S)-2-[[(2R)-2-[[(2S)-2-amino-3-phenylpropanoyl]amino]-3-methylbutanoyl]amino]-3-methylbutanoyl]amino]-3-(4-hydroxyphenyl)propanoic acid
Structure
SMILES: CC(C)[C@H](N=C(O)[C@H](N=C(O)[C@@H](N)CC1=CC=CC=C1)C(C)C)C(O)=N[C@H](CC1=CC=C(O)C=C1)C(=O)O
InChI: InChI=1S/C28H38N4O6/c1-16(2)23(26(35)30-22(28(37)38)15-19-10-12-20(33)13-11-19)32-27(36)24(17(3)4)31-25(34)21(29)14-18-8-6-5-7-9-18/h5-13,16-17,21-24,33H,14-15,29H2,1-4H3,(H,30,35)(H,31,34)(H,32,36)(H,37,38)/t21-,22+,23-,24+/m0/s1
InChIKey: LUVNTPPXXIXEDW-UARRHKHWSA-N
Reference
A tetrapeptide class of biased analgesics from an Australian fungus targets the µ-opioid receptor
PubChem CID: 146682350
LOTUS: LTS0185500
{NPAtlas: NPA025879
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Penicillium sp. | Penicillium | Aspergillaceae | Eurotiales | Eurotiomycetes | Ascomycota | Fungi | Eukaryota |
Properties Information
Molecule Weight: 526.6340000000002
TPSA？: 181.32
MolLogP？: 3.8766000000000025
Number of H-Donors: 6
Number of H-Acceptors: 6
RingCount: 2
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|