BindingDB logo
myBDB logout

null

SMILES: Cc1cc(=O)c(O[C@@H]2O[C@H](COC(=O)CC(C)(O)CC(O)=O)[C@@H](O)[C@H](O)[C@H]2O)cc2CC[C@H](Cc12)C(C)(C)O

InChI Key: InChIKey=VHEIRYSOAGPSSD-TWMDVTLASA-N

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 1 hit for monomerid = 50084417   
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
Reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50084417
PNG
(CHEMBL3426556)
Show SMILES Cc1cc(=O)c(O[C@@H]2O[C@H](COC(=O)CC(C)(O)CC(O)=O)[C@@H](O)[C@H](O)[C@H]2O)cc2CC[C@H](Cc12)C(C)(C)O |r|
Show InChI InChI=1S/C27H38O12/c1-13-7-17(28)18(8-14-5-6-15(9-16(13)14)26(2,3)35)38-25-24(34)23(33)22(32)19(39-25)12-37-21(31)11-27(4,36)10-20(29)30/h7-8,15,19,22-25,32-36H,5-6,9-12H2,1-4H3,(H,29,30)/t15-,19-,22-,23+,24-,25-,27?/m1/s1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>5.00E+4n/an/an/an/an/an/a



Food and Drug Administration

Curated by ChEMBL


Assay Description
Inhibition of human immunodeficiency virus-1 reverse transcriptase associated RNase H activity using using 18-nucleotide 3,-fluorescein-labeled RNA s...


J Nat Prod 78: 315-9 (2015)


Article DOI: 10.1021/np5006696
BindingDB Entry DOI: 10.7270/Q218386T
More data for this
Ligand-Target Pair