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BDBM50343414 CHEMBL1774942::homotemsirolimus C

SMILES: CC[C@@H]1\C=C(C)\[C@@H](O)[C@@H](OC)C(=O)[C@H](C)C[C@H](C)\C=C\C=C\C=C(C)\[C@H](C[C@@H]2CC[C@@H](C)[C@@](O)(O2)C(=O)C(=O)N2CCCC[C@H]2C(=O)O[C@@H](CC1=O)[C@H](C)C[C@@H]1CC[C@@H](OC(=O)C(C)(CO)CO)[C@@H](C1)OC)OC

InChI Key: InChIKey=OZMZZJHYZQVAQQ-IFICCMBESA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50343414   
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
Serine/threonine-protein kinase mTOR


(Homo sapiens (human))
BDBM50343414
PNG
(CHEMBL1774942 | homotemsirolimus C)
Show SMILES CC[C@@H]1\C=C(C)\[C@@H](O)[C@@H](OC)C(=O)[C@H](C)C[C@H](C)\C=C\C=C\C=C(C)\[C@H](C[C@@H]2CC[C@@H](C)[C@@](O)(O2)C(=O)C(=O)N2CCCC[C@H]2C(=O)O[C@@H](CC1=O)[C@H](C)C[C@@H]1CC[C@@H](OC(=O)C(C)(CO)CO)[C@@H](C1)OC)OC
Show InChI InChI=1S/C57H89NO16/c1-12-41-28-38(6)50(63)51(71-11)49(62)37(5)26-34(2)18-14-13-15-19-35(3)46(69-9)30-42-23-21-39(7)57(68,74-42)52(64)53(65)58-25-17-16-20-43(58)54(66)72-47(31-44(41)61)36(4)27-40-22-24-45(48(29-40)70-10)73-55(67)56(8,32-59)33-60/h13-15,18-19,28,34,36-37,39-43,45-48,50-51,59-60,63,68H,12,16-17,20-27,29-33H2,1-11H3/b15-13+,18-14+,35-19+,38-28+/t34-,36-,37-,39-,40+,41-,42+,43+,45-,46+,47+,48-,50-,51+,57-/m1/s1
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 2.10E+3n/an/an/an/an/an/a



Wyeth Research

Curated by ChEMBL


Assay Description
Inhibition of FKBP12-independent human recombinant mTOR expressed in HEK293 cells using His6-S6K1 as a substrate by DELFIA assay


J Nat Prod 74: 547-53 (2011)

More data for this
Ligand-Target Pair