IMPPAT Phytochemical information: 
H-Gly-His-Lys-Ile-Ala-Thr-Phe-Gln-Glu-Arg-OH

H-Gly-His-Lys-Ile-Ala-Thr-Phe-Gln-Glu-Arg-OH
Summary

SMILES: NCCCC[C@@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)O)CCCN=C(N)N)CCC(=O)O)CCC(=O)N)Cc1ccccc1)[C@H](O)C)C)[C@H](CC)C)NC(=O)[C@H](Cc1[nH]cnc1)NC(=O)CN
InChI: InChI=1S/C52H83N17O15/c1-5-27(2)41(68-46(78)32(14-9-10-20-53)63-48(80)37(62-39(72)24-54)23-31-25-58-26-60-31)49(81)61-28(3)43(75)69-42(29(4)70)50(82)67-36(22-30-12-7-6-8-13-30)47(79)65-33(16-18-38(55)71)44(76)64-34(17-19-40(73)74)45(77)66-35(51(83)84)15-11-21-59-52(56)57/h6-8,12-13,25-29,32-37,41-42,70H,5,9-11,14-24,53-54H2,1-4H3,(H2,55,71)(H,58,60)(H,61,81)(H,62,72)(H,63,80)(H,64,76)(H,65,79)(H,66,77)(H,67,82)(H,68,78)(H,69,75)(H,73,74)(H,83,84)(H4,56,57,59)/t27-,28-,29+,32-,33-,34-,35-,36-,37-,41-,42-/m0/s1
InChIKey: YWIIIROWEXGMAF-PBEFRTBXSA-N
DeepSMILES: NCCCC[C@@H]C=O)N[C@H]C=O)N[C@H]C=O)N[C@H]C=O)N[C@H]C=O)N[C@H]C=O)N[C@H]C=O)N[C@H]C=O)O))CCCN=CN)N)))))))))CCC=O)O)))))))CCC=O)N)))))))Ccccccc6))))))))))[C@H]O)C)))))C))))[C@H]CC))C)))))NC=O)[C@H]Cc[nH]cnc5))))))NC=O)CN
Scaffold Graph/Node/Bond level: O=C(CCc1cnc[nH]1)NCC(=O)NCC(=O)NCC(=O)NCC(=O)NCCc1ccccc1
Scaffold Graph/Node level: OC(CCC1CNCN1)NCC(O)NCC(O)NCC(O)NCC(O)NCCC1CCCCC1
Scaffold Graph level: CC(CCCC1CCCCC1)CCC(C)CCC(C)CCC(C)CCC(C)CCC1CCCC1
Functional groups: CC(=O)NC; CC(=O)O; CC(N)=O; CN; CN=C(N)N; CNC(C)=O; CO; c[nH]c; cnc
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Organic Polymers
ClassyFire Class: Polypeptides
NP Classifier Biosynthetic pathway: Amino acids and Peptides
NP Classifier Superclass: Oligopeptides
Synonymous chemical names:
yg-1
External chemical identifiers:
CID:101594432
Chemical structure download


H-Gly-His-Lys-Ile-Ala-Thr-Phe-Gln-Glu-Arg-OH
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 1186.34
Log P RDKit -5.64
Topological polar surface area (Å2) RDKit 544.94
Number of hydrogen bond acceptors RDKit 17
Number of hydrogen bond donors RDKit 18
Number of carbon atoms RDKit 52
Number of heavy atoms RDKit 84
Number of heteroatoms RDKit 32
Number of nitrogen atoms RDKit 17
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 11
Stereochemical complexity RDKit 0.21
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 22
Number of sp3 hybridized carbon atoms RDKit 30
Shape complexity RDKit 0.58
Number of rotatable bonds RDKit 39
Number of aliphatic carbocycles RDKit 0
Number of aliphatic heterocycles RDKit 0
Number of aliphatic rings RDKit 0
Number of aromatic carbocycles RDKit 1
Number of aromatic heterocycles RDKit 1
Number of aromatic rings RDKit 2
Total number of rings RDKit 2
Number of saturated carbocycles RDKit 0
Number of saturated heterocycles RDKit 0
Number of saturated rings RDKit 0
Number of Smallest Set of Smallest Rings (SSSR) RDKit 2


H-Gly-His-Lys-Ile-Ala-Thr-Phe-Gln-Glu-Arg-OH
Drug-likeness properties
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 3
Lipinski’s rule of 5 filter RDKit Failed
Number of Ghose filter violations RDKit 4
Ghose filter RDKit Failed
Veber filter RDKit Bad
Pfizer 3/75 filter RDKit Good
GSK 4/400 filter RDKit Bad
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.0168