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Compile Data Set for Download or QSAR

Found 26 hits of affinity data for UniProtKB/TrEMBL: B5SNJ2    Zinc 0: unavailable per Zinc DB. Zinc 1: purchasable, 2 weeks to supply. Zinc 2: made on demand. Zinc 4: potentially available
Target
(Institution)
LigandTarget
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
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
Calyculin A (4)
PNG
(Calyculin B (19) | Calyculin E (22) | Calyculin F ...)
Show SMILES COC[C@@H](C(O)[C@H](O)C(=O)NCCC(C)c1nc(\C=C\CC2OC3(C[C@@H](O)[C@@H]2C)O[C@H]([C@H](C[C@H](O)C(C)[C@H](O)C(C)\C=C(/C)\C(\C)=C\C=C\C(\C)=C\C#N)OC)[C@H](OP(O)(O)=O)C3(C)C)co1)N(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid

Similars

AffyNet 
Article
PubMed
n/an/a 1.0n/an/an/an/an/an/a



The University of Tokyo



Assay Description
Protein phosphatase inhibitory activity of calyculin derivatives.


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
Hemicalyculin A (5)
PNG
Show SMILES CO[C@@H](C[C@H](O)C(C)[C@H](O)C(C)\C=C(/C)\C(\C)=C\C=C\C(\C)=C\C#N)[C@H]1OC2(C[C@@H](O)[C@H](C)C(C\C=C\C#N)O2)C(C)(C)[C@H]1OP(O)(O)=O
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
ZINC 0
AffyNet 
Article
PubMed
n/an/a 1.0n/an/an/an/an/an/a



The University of Tokyo



Assay Description
Protein phosphatase inhibitory activity of calyculin derivatives.


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
Des-N-methylcalyculin A (20)
PNG
Show SMILES CN[C@@H](COC)C(O)[C@H](O)C(=O)NCCC(C)c1nc(\C=C\CC2OC3(C[C@@H](O)[C@@H]2C)O[C@H]([C@H](C[C@H](O)C(C)[C@H](O)C(C)\C=C(/C)\C(\C)=C\C=C\C(\C)=C\C#N)OC)[C@H](OP(O)(O)=O)C3(C)C)co1
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid

Similars

AffyNet 
Article
PubMed
n/an/a 1.0n/an/an/an/an/an/a



The University of Tokyo



Assay Description
Protein phosphatase inhibitory activity of calyculin derivatives.


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
C1/C34-Calyculin A (15)
PNG
Show SMILES CO[C@@H](C[C@H](O)C(C)[C@H](O)C(C)\C=C(/C)\C(\C)=C\C=C\C(\C)=C\C#N)[C@H]1OC2(C[C@@H](O)[C@H](C)C(C\C=C\c3coc(n3)C(C)CCNC(=O)CO)O2)C(C)(C)[C@H]1OP(O)(O)=O
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid

Similars

AffyNet 
Article
PubMed
n/an/a 1.1n/an/an/an/an/an/a



The University of Tokyo



Assay Description
Protein phosphatase inhibitory activity of calyculin derivatives.


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
Calyculinamide A (18)
PNG
Show SMILES COC[C@@H](C(O)[C@H](O)C(=O)NCCC(C)c1nc(\C=C\CC2OC3(C[C@@H](O)[C@@H]2C)O[C@H]([C@H](C[C@H](O)C(C)[C@H](O)C(C)\C=C(/C)\C(\C)=C\C=C\C(\C)=C\C(N)=O)OC)[C@H](OP(O)(O)=O)C3(C)C)co1)N(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid

Similars

AffyNet 
Article
PubMed
n/an/a 1.5n/an/an/an/an/an/a



The University of Tokyo



Assay Description
Protein phosphatase inhibitory activity of calyculin derivatives.


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
Calyculin A 21-acetate (13)
PNG
Show SMILES COC[C@@H](C(O)[C@H](O)C(=O)NCCC(C)c1nc(\C=C\CC2OC3(C[C@@H](OC(C)=O)[C@@H]2C)O[C@H]([C@H](C[C@H](O)C(C)[C@H](O)C(C)\C=C(/C)\C(\C)=C\C=C\C(\C)=C\C#N)OC)[C@H](OP(O)(O)=O)C3(C)C)co1)N(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid

Similars

AffyNet 
Article
PubMed
n/an/a 2.1n/an/an/an/an/an/a



The University of Tokyo



Assay Description
Protein phosphatase inhibitory activity of calyculin derivatives.


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
Calyculin C (24)
PNG
Show SMILES COC[C@@H](C(O)[C@H](O)C(=O)NC(C)CC(C)c1nc(\C=C\CC2OC3(C[C@@H](O)[C@@H]2C)O[C@H]([C@H](C[C@H](O)C(C)[C@H](O)C(C)\C=C(/C)\C(\C)=C\C=C\C(\C)=C\C#N)OC)[C@H](OP(O)(O)=O)C3(C)C)co1)N(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid

Similars

AffyNet 
Article
PubMed
n/an/a 2.6n/an/an/an/an/an/a



The University of Tokyo



Assay Description
Protein phosphatase inhibitory activity of calyculin derivatives.


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
Calyculin F (23)
PNG
(Calyculin B (19) | Calyculin E (22) | Calyculin F ...)
Show SMILES COC[C@@H](C(O)[C@H](O)C(=O)NCCC(C)c1nc(\C=C\CC2OC3(C[C@@H](O)[C@@H]2C)O[C@H]([C@H](C[C@H](O)C(C)[C@H](O)C(C)\C=C(/C)\C(\C)=C\C=C\C(\C)=C\C#N)OC)[C@H](OP(O)(O)=O)C3(C)C)co1)N(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid

Similars

AffyNet 
Article
PubMed
n/an/a 7.5n/an/an/an/an/an/a



The University of Tokyo



Assay Description
Protein phosphatase inhibitory activity of calyculin derivatives.


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
Calyculin B (19)
PNG
(Calyculin B (19) | Calyculin E (22) | Calyculin F ...)
Show SMILES COC[C@@H](C(O)[C@H](O)C(=O)NCCC(C)c1nc(\C=C\CC2OC3(C[C@@H](O)[C@@H]2C)O[C@H]([C@H](C[C@H](O)C(C)[C@H](O)C(C)\C=C(/C)\C(\C)=C\C=C\C(\C)=C\C#N)OC)[C@H](OP(O)(O)=O)C3(C)C)co1)N(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid

Similars

AffyNet 
Article
PubMed
n/an/a 9.0n/an/an/an/an/an/a



The University of Tokyo



Assay Description
Protein phosphatase inhibitory activity of calyculin derivatives.


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
Calyculin E (22)
PNG
(Calyculin B (19) | Calyculin E (22) | Calyculin F ...)
Show SMILES COC[C@@H](C(O)[C@H](O)C(=O)NCCC(C)c1nc(\C=C\CC2OC3(C[C@@H](O)[C@@H]2C)O[C@H]([C@H](C[C@H](O)C(C)[C@H](O)C(C)\C=C(/C)\C(\C)=C\C=C\C(\C)=C\C#N)OC)[C@H](OP(O)(O)=O)C3(C)C)co1)N(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid

Similars

AffyNet 
Article
PubMed
n/an/a 14.0n/an/an/an/an/an/a



The University of Tokyo



Assay Description
Protein phosphatase inhibitory activity of calyculin derivatives.


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
Calyculin J (14)
PNG
Show SMILES CC[C@H](O)CC1(OCC\C=C\c2coc(n2)C(C)CCNC(=O)[C@@H](O)C(O)[C@H](COC)N(C)C)O[C@H]([C@H](C[C@H](O)C(C)C2OC(C)([C@H](Br)[C@H]2C)C(\C)=C\C=C\C(\C)=C\C#N)OC)[C@H](OP(O)(O)=O)C1(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid

Similars

AffyNet 
Article
PubMed
n/an/a 20.0n/an/an/an/an/an/a



The University of Tokyo



Assay Description
Protein phosphatase inhibitory activity of calyculin derivatives.


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
CHEMBL40248
PNG
(10-[3,9-dimethyl-8-(3-methyl-4-oxopentyl)-(9R)-1,7...)
Show SMILES CO[C@@H]([C@H](O)CC(=O)[C@@H](C)[C@@H](O)CC[C@@H](C)[C@@H]1O[C@]2(CC[C@@H](C)[C@H](CC[C@H](C)C(C)=O)O2)CC[C@@H]1C)[C@H](OC(=O)C[C@H](O)C1=C(C)C(=O)OC1=O)C(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
ZINC 0

Similars

AffyNet 
Article
PubMed
n/an/a 500.0n/an/an/an/an/an/a



University of California at Irvine

Curated by ChEMBL


Assay Description
Inhibition of protein phosphatase 2A (PP2A) was determined by standard phosphorylase a inhibition assay


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
CHEMBL295239
PNG
((E)-(R)-4-Hydroxy-2-methyl-hex-2-enedioic acid 6-{...)
Show SMILES CO[C@@H]([C@H](O)CC(=O)[C@@H](C)[C@@H](O)CC[C@@H](C)[C@@H]1O[C@]2(CC[C@@H](C)[C@H](CC[C@H](C)C(C)=O)O2)CC[C@@H]1C)[C@H](OC(=O)C[C@@H](O)\C=C(/C)C(O)=O)C(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
ZINC 0

Similars

AffyNet 
Article
PubMed
n/an/a 4000.0n/an/an/an/an/an/a



University of California at Irvine

Curated by ChEMBL


Assay Description
Inhibition of protein phosphatase 2A (PP2A) was determined by standard phosphorylase a inhibition assay


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
TAUTOMYCIN
PNG
Show SMILES CO[C@H]([C@H](O)CC(=O)[C@@H](C)[C@@H](O)CC[C@@H](C)[C@@H]1O[C@]2(CC[C@@H](C)[C@H](CC[C@H](C)C(C)=O)O2)CC[C@@H]1C)[C@H](OC(=O)C[C@@H](O)C1=C(C)C(=O)OC1=O)C(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
ZINC 0

Similars

AffyNet 
Article
PubMed
n/an/a 9400.0n/an/an/an/an/an/a



University of California at Irvine

Curated by ChEMBL


Assay Description
Inhibition of protein phosphatase 2A (PP2A) was determined by standard phosphorylase a inhibition assay


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
Calyculin A 11,13,21-triacetate (12)
PNG
Show SMILES COC[C@@H](C(O)[C@H](O)C(=O)NCCC(C)c1nc(\C=C\CC2OC3(C[C@@H](OC(C)=O)[C@@H]2C)O[C@H]([C@H](C[C@H](OC(C)=O)C(C)[C@H](OC(C)=O)C(C)\C=C(/C)\C(\C)=C\C=C\C(\C)=C\C#N)OC)[C@H](OP(O)(O)=O)C3(C)C)co1)N(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid

Similars

AffyNet 
Article
PubMed
n/an/a>10000.0n/an/an/an/an/an/a



The University of Tokyo



Assay Description
Protein phosphatase inhibitory activity of calyculin derivatives.


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
C9/C35-calyculin (16)
PNG
Show SMILES CO[C@@H](C[C@H](O)C(C)[C@H](O)C(C)CO)[C@H]1OC2(C[C@@H](O)[C@H](C)C(CCO)O2)C(C)(C)[C@H]1OP(O)(O)=O
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
ZINC 0
AffyNet 
Article
PubMed
n/an/a>10000.0n/an/an/an/an/an/a



The University of Tokyo



Assay Description
Protein phosphatase inhibitory activity of calyculin derivatives.


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
11,13-O-isopropylidene-calyculin A (6)
PNG
Show SMILES COC[C@@H](C(O)[C@H](O)C(=O)NCCC(C)c1nc(\C=C\CC2OC3(C[C@@H](O)[C@@H]2C)O[C@H]([C@H](C[C@@H]2OC(C)(C)O[C@H](C(C)\C=C(/C)\C(\C)=C\C=C\C(\C)=C\C#N)C2C)OC)[C@H](OP(O)(O)=O)C3(C)C)co1)N(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid

Similars

AffyNet 
Article
PubMed
n/an/a>10000.0n/an/an/an/an/an/a



The University of Tokyo



Assay Description
Protein phosphatase inhibitory activity of calyculin derivatives.


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
Dephosphonocalyculin A (17)
PNG
Show SMILES COC[C@@H](C(O)[C@H](O)C(=O)NCCC(C)c1nc(\C=C\CC2OC3(C[C@@H](O)[C@@H]2C)O[C@H]([C@H](C[C@H](O)C(C)[C@H](O)C(C)\C=C(/C)\C(\C)=C\C=C\C(\C)=C\C#N)OC)[C@H](O)C3(C)C)co1)N(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid

Similars

AffyNet 
Article
PubMed
n/an/a>10000.0n/an/an/an/an/an/a



The University of Tokyo



Assay Description
Protein phosphatase inhibitory activity of calyculin derivatives.


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
CHEMBL602231
PNG
(2-(2-Carboxy-benzoylamino)-4-(30-chloro-40-fluorob...)
Show SMILES CCOC(=O)c1c(NC(=O)c2ccccc2C(O)=O)scc1-c1ccc(cc1)-c1ccc(F)c(Cl)c1
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
ZINC 0

Similars

AffyNet 
Article
PubMed
n/an/a 23100.0n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of PTPalpha expressed in Escherichia coli BL21 (DE3) after 10 mins by spectrophotometry


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
CHEMBL40247
PNG
((S)-2-Hydroxy-2-methyl-succinic acid 4-{(1R,2S,3R,...)
Show SMILES CO[C@@H]([C@H](O)CC(=O)[C@@H](C)[C@@H](O)CC[C@@H](C)[C@@H]1O[C@]2(CC[C@@H](C)[C@H](CC[C@H](C)C(C)=O)O2)CC[C@@H]1C)[C@H](OC(=O)C[C@](C)(O)C(O)=O)C(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
ZINC 0

Similars

AffyNet 
Article
PubMed
n/an/a 29000.0n/an/an/an/an/an/a



University of California at Irvine

Curated by ChEMBL


Assay Description
Inhibition of protein phosphatase 2A (PP2A) was determined by standard phosphorylase a inhibition assay


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
CHEMBL599646
PNG
(4-Biphenyl-4-yl-2-(2-carboxy-benzoylamino)-5-methy...)
Show SMILES CCOC(=O)c1c(NC(=O)c2ccccc2C(O)=O)scc1-c1ccc(cc1)-c1ccccc1
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
ZINC 0

Similars

AffyNet 
Article
PubMed
n/an/a 49700.0n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of PTPalpha expressed in Escherichia coli BL21 (DE3) after 10 mins by spectrophotometry


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
CHEMBL598217
PNG
(4-Biphenyl-4-yl-2-[(3-carboxy-bicyclo[2.2.1]hept-5...)
Show SMILES CC(C)OC(=O)c1c(NC(=O)C2C3CC(C=C3)C2C(O)=O)scc1-c1ccc(cc1)-c1ccccc1
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
ZINC 0

Similars

AffyNet 
Article
PubMed
n/an/a>100000.0n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of PTPalpha expressed in Escherichia coli BL21 (DE3) after 10 mins by spectrophotometry


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
CHEMBL603479
PNG
(2-[(3-Carboxy-bicyclo[2.2.1]hept-5-ene-2-carbonyl)...)
Show SMILES CC(C)OC(=O)c1c(NC(=O)C2C3CC(C=C3)C2C(O)=O)scc1-c1ccc(cc1)-c1ccc(Cl)cc1
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
ZINC 0

Similars

AffyNet 
Article
PubMed
n/an/a>100000.0n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of PTPalpha expressed in Escherichia coli BL21 (DE3) after 10 mins by spectrophotometry


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
CHEMBL598832
PNG
(3-(3,5-dibromo-4-hydroxybenzoyl)-2-ethyl-N-(thiazo...)
Show SMILES CCc1oc2cc(ccc2c1C(=O)c1cc(Br)c(O)c(Br)c1)S(=O)(=O)Nc1nccs1
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
ZINC 0

Similars

AffyNet 
Article
PubMed
n/an/a>100000.0n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of PTPalpha expressed in Escherichia coli BL21 (DE3) after 10 mins by spectrophotometry


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
CHEMBL295238
PNG
((R)-2-Hydroxy-2-methyl-succinic acid 4-{(1R,2S,3R,...)
Show SMILES CO[C@@H]([C@H](O)CC(=O)[C@@H](C)[C@@H](O)CC[C@@H](C)[C@@H]1O[C@]2(CC[C@@H](C)[C@H](CC[C@H](C)C(C)=O)O2)CC[C@@H]1C)[C@H](OC(=O)C[C@@](C)(O)C(O)=O)C(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
ZINC 0

Similars

AffyNet 
Article
PubMed
n/an/a 100000.0n/an/an/an/an/an/a



University of California at Irvine

Curated by ChEMBL


Assay Description
Inhibition of protein phosphatase 2A (PP2A) was determined by standard phosphorylase a inhibition assay


Citation and Details
More data for this
Ligand-Target Pair
Protein phosphatase 2A regulatory subunit B'


(Homo sapiens)
CHEMBL40659
PNG
(4-Phosphono-butyric acid (1R,2S,3R,6S,7S,10R)-10-[...)
Show SMILES CO[C@@H]([C@H](O)CC(=O)[C@@H](C)[C@@H](O)CC[C@@H](C)[C@@H]1O[C@]2(CC[C@@H](C)[C@H](CC[C@H](C)C(C)=O)O2)CC[C@@H]1C)[C@H](OC(=O)CCCP(O)(O)=O)C(C)C
PDB
MMDB

NCI pathway

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
ZINC 0
AffyNet 
Article
PubMed
n/an/a 300000.0n/an/an/an/an/an/a



University of California at Irvine

Curated by ChEMBL


Assay Description
Inhibition of protein phosphatase 2A (PP2A) was determined by standard phosphorylase a inhibition assay


Citation and Details
More data for this
Ligand-Target Pair