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SMILES: CN(CCCn1cnc2cc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)c3CCCc3c12)C1CC[C@@H](CC1)OC(=O)[C@](O)(c1cccs1)c1ccc(C)s1

InChI Key:

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 624965   
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
Beta-2 adrenergic receptor


(Homo sapiens (Human))
BDBM624965
PNG
(US20230322745, Compound 38)
Show SMILES CN(CCCn1cnc2cc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)c3CCCc3c12)C1CC[C@@H](CC1)OC(=O)[C@](O)(c1cccs1)c1ccc(C)s1 |r,wU:43.49,wD:14.14,37.45,43.50,(3.77,1.68,;4.17,3.17,;3.08,4.26,;1.59,3.86,;.5,4.95,;-.98,4.55,;-1.61,3.15,;-3.14,3.31,;-3.46,4.81,;-4.8,5.58,;-4.8,7.12,;-6.13,7.89,;-7.46,7.12,;-8.8,7.89,;-10.13,7.12,;-10.13,5.58,;-11.46,7.89,;-12.8,7.12,;-14.13,7.89,;-14.13,9.43,;-15.46,10.2,;-12.8,10.2,;-12.8,11.74,;-11.46,12.51,;-11.46,14.05,;-10.13,11.74,;-10.13,10.2,;-11.46,9.43,;-3.46,7.89,;-3.14,9.4,;-1.61,9.56,;-.98,8.15,;-2.13,7.12,;-2.13,5.58,;5.66,3.57,;6.06,5.06,;7.54,5.46,;8.63,4.37,;8.23,2.88,;6.75,2.48,;10.12,4.77,;10.52,6.25,;9.43,7.34,;12.01,6.65,;13.49,7.05,;12.4,8.14,;11.44,9.34,;12.27,10.63,;13.76,10.23,;13.84,8.69,;13.09,5.56,;14.56,6.04,;15.46,4.79,;14.56,3.55,;15.04,2.08,;13.09,4.02,)|
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 13.5n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Muscarinic acetylcholine receptor M2


(Homo sapiens (Human))
BDBM624965
PNG
(US20230322745, Compound 38)
Show SMILES CN(CCCn1cnc2cc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)c3CCCc3c12)C1CC[C@@H](CC1)OC(=O)[C@](O)(c1cccs1)c1ccc(C)s1 |r,wU:43.49,wD:14.14,37.45,43.50,(3.77,1.68,;4.17,3.17,;3.08,4.26,;1.59,3.86,;.5,4.95,;-.98,4.55,;-1.61,3.15,;-3.14,3.31,;-3.46,4.81,;-4.8,5.58,;-4.8,7.12,;-6.13,7.89,;-7.46,7.12,;-8.8,7.89,;-10.13,7.12,;-10.13,5.58,;-11.46,7.89,;-12.8,7.12,;-14.13,7.89,;-14.13,9.43,;-15.46,10.2,;-12.8,10.2,;-12.8,11.74,;-11.46,12.51,;-11.46,14.05,;-10.13,11.74,;-10.13,10.2,;-11.46,9.43,;-3.46,7.89,;-3.14,9.4,;-1.61,9.56,;-.98,8.15,;-2.13,7.12,;-2.13,5.58,;5.66,3.57,;6.06,5.06,;7.54,5.46,;8.63,4.37,;8.23,2.88,;6.75,2.48,;10.12,4.77,;10.52,6.25,;9.43,7.34,;12.01,6.65,;13.49,7.05,;12.4,8.14,;11.44,9.34,;12.27,10.63,;13.76,10.23,;13.84,8.69,;13.09,5.56,;14.56,6.04,;15.46,4.79,;14.56,3.55,;15.04,2.08,;13.09,4.02,)|
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/a 0.842n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Muscarinic acetylcholine receptor M3


(Homo sapiens (Human))
BDBM624965
PNG
(US20230322745, Compound 38)
Show SMILES CN(CCCn1cnc2cc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)c3CCCc3c12)C1CC[C@@H](CC1)OC(=O)[C@](O)(c1cccs1)c1ccc(C)s1 |r,wU:43.49,wD:14.14,37.45,43.50,(3.77,1.68,;4.17,3.17,;3.08,4.26,;1.59,3.86,;.5,4.95,;-.98,4.55,;-1.61,3.15,;-3.14,3.31,;-3.46,4.81,;-4.8,5.58,;-4.8,7.12,;-6.13,7.89,;-7.46,7.12,;-8.8,7.89,;-10.13,7.12,;-10.13,5.58,;-11.46,7.89,;-12.8,7.12,;-14.13,7.89,;-14.13,9.43,;-15.46,10.2,;-12.8,10.2,;-12.8,11.74,;-11.46,12.51,;-11.46,14.05,;-10.13,11.74,;-10.13,10.2,;-11.46,9.43,;-3.46,7.89,;-3.14,9.4,;-1.61,9.56,;-.98,8.15,;-2.13,7.12,;-2.13,5.58,;5.66,3.57,;6.06,5.06,;7.54,5.46,;8.63,4.37,;8.23,2.88,;6.75,2.48,;10.12,4.77,;10.52,6.25,;9.43,7.34,;12.01,6.65,;13.49,7.05,;12.4,8.14,;11.44,9.34,;12.27,10.63,;13.76,10.23,;13.84,8.69,;13.09,5.56,;14.56,6.04,;15.46,4.79,;14.56,3.55,;15.04,2.08,;13.09,4.02,)|
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/a 0.555n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair