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Assay Detail

CHEMBL2049250

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibition of Cryptococcus neoformans Can2 preincubated for 15 mins measured for 10 to 100 sec by stopped-flow method
41
Total Activities
41
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Cryptococcus neoformans
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Carbonic anhydrase 2 (CHEMBL1697676)
Type SINGLE PROTEIN
Organism Cryptococcus neoformans var. grubii

Publication

Molecular cloning, characterization, and inhibition studies of a β-carbonic anhydrase from Malassezia globosa, a potential antidandruff target.
Hewitson KS, Vullo D, Scozzafava A, Mastrolorenzo A, Supuran CT.
J Med Chem (2012) 55 : 3513 -3520
PubMed 22424239 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 41 6.25 7.98

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL20 ACETAZOLAMIDE 4.0 1 7.98
CHEMBL73962 BENZOLAMIDE 1 7.64
CHEMBL268439 1 7.38
CHEMBL19 METHAZOLAMIDE 4.0 1 7.20
CHEMBL220491 BRINZOLAMIDE 4.0 1 7.06
CHEMBL18 ETHOXZOLAMIDE 4.0 1 7.06
CHEMBL266240 1 6.52
CHEMBL283121 1 6.46
CHEMBL220492 TOPIRAMATE 4.0 1 6.43
CHEMBL6705 1 6.42
CHEMBL360356 1 6.42
CHEMBL166686 1 6.39
CHEMBL451332 1 6.36
CHEMBL414 CARZENIDE 2.0 1 6.32
CHEMBL7092 1 6.22
CHEMBL7146 1 6.21
CHEMBL6919 1 6.21
CHEMBL178852 1 6.21
CHEMBL268177 1 6.15
CHEMBL865 VALDECOXIB 4.0 1 6.15
CHEMBL24259 PHENYLSULFAMATE 1 6.15
CHEMBL168514 PHENYLSULFAMIDE 1 6.14
CHEMBL27601 BENZENESULFONAMIDE 1 6.13
CHEMBL21 SULFANILAMIDE 4.0 1 6.12
CHEMBL265674 1 6.10
CHEMBL6753 1 6.09
CHEMBL6853 1 6.09
CHEMBL26 SULPIRIDE 3.0 1 6.09
CHEMBL6784 1 6.06
CHEMBL77517 INDISULAM 2.0 1 6.02

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL20 ACETAZOLAMIDE Ki = 10.5 nM 7.98
CHEMBL73962 BENZOLAMIDE Ki = 23.0 nM 7.64
CHEMBL268439 Ki = 42.0 nM 7.38
CHEMBL19 METHAZOLAMIDE Ki = 63.0 nM 7.20
CHEMBL220491 BRINZOLAMIDE Ki = 87.0 nM 7.06
CHEMBL18 ETHOXZOLAMIDE Ki = 87.0 nM 7.06
CHEMBL266240 Ki = 300.0 nM 6.52
CHEMBL283121 Ki = 345.0 nM 6.46
CHEMBL220492 TOPIRAMATE Ki = 367.0 nM 6.43
CHEMBL360356 Ki = 379.0 nM 6.42
CHEMBL6705 Ki = 379.0 nM 6.42
CHEMBL166686 Ki = 410.0 nM 6.39
CHEMBL451332 Ki = 440.0 nM 6.36
CHEMBL414 CARZENIDE Ki = 484.0 nM 6.32
CHEMBL7092 Ki = 605.0 nM 6.22
CHEMBL7146 Ki = 624.0 nM 6.21
CHEMBL178852 Ki = 612.0 nM 6.21
CHEMBL6919 Ki = 623.0 nM 6.21
CHEMBL24259 PHENYLSULFAMATE Ki = 703.0 nM 6.15
CHEMBL268177 Ki = 711.0 nM 6.15
CHEMBL865 VALDECOXIB Ki = 704.0 nM 6.15
CHEMBL168514 PHENYLSULFAMIDE Ki = 731.0 nM 6.14
CHEMBL27601 BENZENESULFONAMIDE Ki = 746.0 nM 6.13
CHEMBL21 SULFANILAMIDE Ki = 765.0 nM 6.12
CHEMBL265674 Ki = 791.0 nM 6.10
CHEMBL6753 Ki = 815.0 nM 6.09
CHEMBL6853 Ki = 809.0 nM 6.09
CHEMBL26 SULPIRIDE Ki = 812.0 nM 6.09
CHEMBL6784 Ki = 878.0 nM 6.06
CHEMBL77517 INDISULAM Ki = 963.0 nM 6.02
CHEMBL266026 Ki = 971.0 nM 6.01
CHEMBL750 ZONISAMIDE Ki = 971.0 nM 6.01
CHEMBL6724 Ki = 977.0 nM 6.01
CHEMBL418 2,4-DISULFAMYLTRIFLUOROMETHYLANILINE Ki = 968.0 nM 6.01
CHEMBL574 P-TOLUENESULFONAMIDE Ki = 1150.0 nM 5.94
CHEMBL17 DICHLORPHENAMIDE Ki = 1203.0 nM 5.92
CHEMBL7087 Ki = 1394.0 nM 5.86
CHEMBL118 CELECOXIB Ki = 3056.0 nM 5.51
CHEMBL6633 Ki = 3887.0 nM 5.41
CHEMBL218490 DORZOLAMIDE Ki = 8347.0 nM 5.08
CHEMBL419 MAFENIDE Ki = 18490.0 nM 4.73