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Compile Data Set for Download or QSAR

Found 1 hit Enz. Inhib. hit(s) with Target = 'Orexin/Hypocretin receptor type 1' and Ligand = 'BDBM50121781'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Orexin/Hypocretin receptor type 1


(Homo sapiens (Human))
BDBM50121781
PNG
(CHEMBL275985 | [Gly22]orexin-B)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@@H](N)CCSC)[C@@H](C)O)C(=O)NCC(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(N)=O)C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCC(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CCCN=C(N)N)C(N)=O |wU:78.78,73.74,67.67,123.123,55.55,103.103,2.2,8.12,185.187,20.20,87.87,wD:131.131,155.155,191.193,114.114,45.44,36.36,146.146,4.4,95.95,16.16,26.27,170.172,177.180,(18.08,-21.19,;18.08,-22.73,;16.75,-23.5,;15.41,-22.73,;16.75,-25.04,;18.08,-25.81,;19.41,-25.04,;19.41,-23.5,;20.75,-25.81,;20.75,-27.35,;19.41,-28.12,;19.41,-29.66,;18.08,-27.35,;22.08,-25.04,;23.42,-25.81,;23.42,-27.35,;24.76,-25.04,;26.09,-25.81,;27.42,-25.04,;27.42,-23.5,;28.76,-25.81,;30.09,-25.04,;28.76,-27.35,;27.42,-28.12,;27.43,-29.66,;26.11,-30.44,;24.76,-23.5,;26.09,-22.73,;23.42,-22.73,;15.41,-25.81,;15.41,-27.35,;14.09,-25.05,;12.76,-25.82,;11.42,-25.05,;11.42,-23.51,;10.08,-25.82,;8.75,-25.05,;8.75,-23.51,;7.41,-25.82,;7.41,-27.36,;6.08,-25.05,;4.75,-25.82,;3.41,-25.05,;3.41,-23.51,;2.08,-25.82,;.75,-25.05,;.75,-23.51,;-.59,-22.74,;-1.82,-23.68,;-3.08,-22.8,;-2.65,-21.33,;-1.11,-21.29,;-.59,-25.82,;-.59,-27.36,;-1.93,-25.05,;-3.26,-25.82,;-3.26,-27.36,;-4.6,-28.13,;-5.93,-27.36,;-4.6,-29.67,;-4.6,-25.05,;-4.6,-23.51,;-5.93,-25.82,;-7.25,-25.06,;-7.25,-23.52,;-5.92,-22.75,;-8.59,-22.75,;-8.56,-21.23,;-9.85,-20.43,;-9.81,-18.89,;-7.19,-20.49,;-5.88,-21.29,;-7.16,-18.95,;-5.83,-18.18,;-5.83,-16.64,;-4.49,-18.95,;-4.49,-20.49,;-3.15,-18.18,;-3.17,-16.64,;-4.51,-15.88,;-4.52,-14.34,;-5.85,-13.58,;-7.16,-14.36,;-5.86,-12.03,;-1.82,-15.87,;-1.84,-14.33,;-.49,-16.63,;.84,-15.86,;.84,-14.32,;2.18,-13.55,;2.18,-12.01,;3.51,-14.32,;2.18,-16.63,;2.18,-18.17,;3.51,-15.86,;4.84,-16.63,;4.84,-18.17,;6.18,-18.94,;6.18,-20.48,;7.51,-18.17,;6.18,-15.86,;6.18,-14.32,;7.52,-16.63,;8.85,-15.86,;8.85,-14.32,;10.19,-13.55,;10.19,-12.01,;11.53,-11.26,;12.86,-12.03,;14.19,-11.26,;12.86,-13.57,;10.19,-16.63,;10.19,-18.17,;11.51,-15.85,;12.84,-16.62,;12.84,-18.16,;14.18,-18.93,;14.18,-20.47,;15.51,-21.24,;12.84,-21.24,;14.18,-15.85,;14.18,-14.31,;15.52,-16.62,;16.85,-15.85,;16.85,-14.31,;18.19,-13.54,;18.19,-12,;19.52,-14.31,;18.19,-16.62,;18.19,-18.16,;19.52,-15.85,;20.85,-16.62,;20.85,-18.16,;22.19,-18.93,;22.19,-20.47,;23.53,-21.24,;24.86,-20.47,;26.19,-21.24,;24.86,-18.94,;22.19,-15.85,;22.19,-14.31,;23.52,-16.62,;24.86,-15.87,;24.86,-14.32,;23.53,-13.55,;26.19,-13.56,;26.2,-12.02,;27.54,-11.26,;27.55,-9.71,;28.89,-8.95,;28.9,-7.42,;30.22,-9.74,;24.87,-11.23,;23.53,-11.99,;24.88,-9.69,;23.55,-8.92,;23.57,-7.4,;24.91,-6.63,;24.91,-5.09,;26.24,-7.4,;22.21,-9.69,;22.21,-11.23,;20.88,-8.92,;19.55,-9.69,;18.22,-8.92,;16.89,-9.7,;18.22,-7.38,;19.47,-6.47,;18.99,-5.01,;17.45,-5.01,;16.97,-6.47,;15.64,-7.26,;15.66,-8.8,;14.3,-6.51,;13.82,-5.05,;12.28,-5.05,;11.81,-6.51,;13.05,-7.42,;13.05,-8.96,;14.39,-9.73,;11.71,-9.74,;10.38,-8.97,;9.04,-9.74,;9.04,-11.28,;7.71,-8.97,;6.38,-9.74,;6.38,-11.28,;5.04,-12.05,;5.04,-8.97,;5.04,-7.43,;3.71,-9.74,;2.38,-8.97,;2.38,-7.43,;1.04,-6.66,;1.04,-5.12,;-.27,-4.35,;-1.61,-5.12,;-2.94,-4.35,;-1.61,-6.65,;1.04,-9.74,;-.29,-8.97,;1.04,-11.28,)|
Show InChI InChI=1S/C122H210N44O35S/c1-17-63(12)96(163-113(195)79(45-62(10)11)162-118(200)97(66(15)169)164-101(183)68(123)34-40-202-16)117(199)143-49-90(174)146-64(13)99(181)139-50-92(176)149-80(46-67-48-135-57-145-67)112(194)161-81(47-89(127)173)104(186)141-52-93(177)150-82(55-167)114(196)147-65(14)100(182)153-73(29-32-87(125)171)107(189)159-78(44-61(8)9)111(193)160-77(43-60(6)7)110(192)155-71(25-20-37-138-122(133)134)105(187)156-74(30-33-88(126)172)108(190)158-76(42-59(4)5)109(191)154-70(24-19-36-137-121(131)132)102(184)140-51-91(175)148-72(28-31-86(124)170)106(188)157-75(41-58(2)3)103(185)144-54-95(179)165-38-22-27-85(165)119(201)166-39-21-26-84(166)116(198)142-53-94(178)151-83(56-168)115(197)152-69(98(128)180)23-18-35-136-120(129)130/h48,57-66,68-85,96-97,167-169H,17-47,49-56,123H2,1-16H3,(H2,124,170)(H2,125,171)(H2,126,172)(H2,127,173)(H2,128,180)(H,135,145)(H,139,181)(H,140,184)(H,141,186)(H,142,198)(H,143,199)(H,144,185)(H,146,174)(H,147,196)(H,148,175)(H,149,176)(H,150,177)(H,151,178)(H,152,197)(H,153,182)(H,154,191)(H,155,192)(H,156,187)(H,157,188)(H,158,190)(H,159,189)(H,160,193)(H,161,194)(H,162,200)(H,163,195)(H,164,183)(H4,129,130,136)(H4,131,132,137)(H4,133,134,138)/t63-,64-,65-,66+,68-,69-,70-,71-,72-,73-,74-,75-,76-,77-,78-,79-,80-,81-,82-,83-,84-,85-,96-,97-/m0/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/an/an/a 7.5n/an/an/an/a



Banyu Tsukuba Research Institute

Curated by ChEMBL


Assay Description
Agonist activity against human orexin 1 receptor; EC50; nM


Bioorg Med Chem Lett 13: 111-3 (2002)


BindingDB Entry DOI: 10.7270/Q2HD7V0D
More data for this
Ligand-Target Pair