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SMILES: CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@@H]1CCCN1C(=O)CCc1ccc(F)cc1

InChI Key: InChIKey=YLAJGYGPVRSAJK-OOPKDDOGSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50470117   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470117
PNG
(CHEMBL264989)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@@H]1CCCN1C(=O)CCc1ccc(F)cc1 |wU:57.63,12.20,wD:63.66,45.57,31.44,23.28,5.4,(20.41,-5.17,;20.43,-6.7,;19.11,-7.49,;17.76,-6.71,;16.46,-7.49,;17.73,-5.22,;18.94,-4.33,;18.43,-2.88,;16.89,-2.9,;16.47,-4.33,;15.14,-5.09,;15.14,-6.64,;13.8,-4.33,;13.82,-2.78,;15.15,-2.01,;15.18,-.48,;16.51,.28,;16.53,1.83,;17.86,2.58,;15.19,2.6,;12.48,-5.07,;11.15,-4.3,;11.16,-2.75,;9.81,-5.06,;9.79,-6.6,;11.13,-7.39,;12.45,-6.62,;11.09,-8.92,;8.47,-4.29,;7.13,-5.04,;7.13,-6.57,;5.81,-4.26,;5.84,-2.72,;5.36,-1.27,;3.9,-.78,;3.9,.76,;5.36,1.25,;6,2.63,;7.52,2.79,;8.44,1.55,;7.8,.13,;6.26,-.01,;4.49,-5.03,;3.14,-4.25,;3.14,-2.71,;1.8,-5,;1.8,-6.54,;3.13,-7.32,;4.46,-6.55,;5.8,-7.35,;5.78,-8.89,;7.1,-9.64,;4.45,-9.64,;3.1,-8.87,;.48,-4.22,;-.86,-4.97,;-.86,-6.52,;-2.18,-4.2,;-2.16,-2.67,;-.84,-1.91,;-3.51,-4.96,;-4.85,-4.19,;-4.83,-2.65,;-6.15,-4.93,;-6.43,-6.44,;-7.96,-6.64,;-8.62,-5.23,;-7.53,-4.17,;-8.3,-2.65,;-7.24,-1.36,;-9.62,-1.85,;-11.1,-2.72,;-12.62,-1.87,;-14.1,-2.74,;-15.57,-1.9,;-15.57,-.17,;-17.05,.76,;-14.1,.7,;-12.62,-.14,)|
Show InChI InChI=1S/C56H75FN12O10/c1-4-60-53(77)46-13-9-27-69(46)55(79)41(12-7-25-61-56(58)59)63-49(73)42(28-33(2)3)64-51(75)44(30-36-31-62-40-11-6-5-10-39(36)40)66-50(74)43(29-35-17-22-38(71)23-18-35)65-52(76)45(32-70)67-54(78)47-14-8-26-68(47)48(72)24-19-34-15-20-37(57)21-16-34/h5-6,10-11,15-18,20-23,31,33,41-47,62,70-71H,4,7-9,12-14,19,24-30,32H2,1-3H3,(H,60,77)(H,63,73)(H,64,75)(H,65,76)(H,66,74)(H,67,78)(H4,58,59,61)/t41-,42-,43-,44+,45-,46+,47-/m0/s1
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
0.0120n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair