[3H]NPY (human, mouse, rat) [8011]
[3H]NPY (human, mouse, rat)
| SMILES |
CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](C)NC(=O)[C@H](CCSC)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O)[C@@H](C)O)[C@@H](C)CC |
| InChIKey |
XKWCTHKJQNUFOQ-HRPSIEBRSA-N |
| Sequence |
YPSKPDNPGEDAPAEDMARYYSALRHYINLITRQRY |
| HELM |
PEPTIDE1{Y.P.S.K.P.D.N.P.G.E.D.A.P.A.E.D.M.A.R.Y.Y.S.A.L.R.H.Y.I.N.L.I.T.R.Q.R.Y.[am]}$$$$ |
Chemical Properties
| Hydrogen bond acceptors |
60 |
| Hydrogen bond donors |
59 |
| Rotatable bonds |
132 |
| Log P |
-18.974 |
| Molecular weight (Da) |
4269.1 |
| Stereochemistry info |
partial |
| Radioactive |
3H |
Bioactivities
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| Receptor |
Activity |
Source |
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Gene |
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Type |
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| Receptor |
Activity |
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| Protein |
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[3H]NPY (human, mouse, rat)
Drug properties
| Molecular type |
Peptide |
| Physiological/Surrogate |
Surrogate |
| Approved drug |
No |
Distribution across phases (no. indications)
Phase I
0
Phase II
0
Phase III
0
Phase IV
0
Compound is not listed as a drug.