Butyl(Butylsulfamoyl)Amine

Butyl(Butylsulfamoyl)Amine

SCHEMBL2486301

CCCCNS(=O)(=O)NCCCC

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA1 P00915 5/20 1.00
CA2 P00918 5/20 1.00
CA12 O43570 3/20 1.00
CA14 Q9ULX7 3/20 1.00
CA7 P43166 2/20 1.00
PPARA Q07869 4/20 0.73
CA9 Q16790 1/20 0.53
EPHX1 P07099 1/20 0.46
MEN1 O00255 1/20 0.43
HTT P42858 1/20 0.43
KMT2A Q03164 1/20 0.43
PSEN1 P49768 1/20 0.42
PSEN2 P49810 1/20 0.42
APH1B Q8WW43 1/20 0.42
NCSTN Q92542 1/20 0.42
APH1A Q96BI3 1/20 0.42
PSENEN Q9NZ42 1/20 0.42
ADH1B P00325 1/20 0.42
ADH1C P00326 1/20 0.42
ADH1A P07327 1/20 0.42

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL4563383 0.92 PPARA (0.86) CA1CA2CA12CA14CA7
SCHEMBL3792249 0.89 PPARA (0.91) CA1CA2CA12CA14CA7
SCHEMBL9285865 0.89 PPARA (0.91) CA1CA2CA12CA14CA7
SCHEMBL10892940 0.89 PPARA (0.91) CA1CA2CA12CA14CA7
SCHEMBL19115006 0.87 CA1 (0.76) CA1CA2CA12CA14CA7
SCHEMBL3119510 0.85 PPARA (1.00) CA1CA2CA12CA14CA7
SCHEMBL3120899 0.85 PPARA (1.00) CA1CA2CA12CA14CA7
SCHEMBL3117611 0.85 PPARA (1.00) CA1CA2CA12CA14CA7
SCHEMBL18644318 0.85 PPARA (1.00) CA1CA2CA12CA14CA7
SCHEMBL27777946 0.85 CA1 (0.83) CA1CA2CA12CA14CA7

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 16 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2380882-B1 Salts of heterocyclic anions and their uses as ionic conductive materials HYDRO QUEBEC (CA) 2012-08-15 EP disclosed
EP-2380882-A1 Salts of heterocyclic anions and their uses as ionic conductive materials HYDRO QUEBEC (CA) 2011-10-26 EP disclosed
US-7229738-B2 Silver halide photographic light-sensitive material FUJIFILM CORPORATION (JP) 2007-06-12 US disclosed
US-7172855-B2 Silver halide photographic light-sensitive material and package thereof FUJI PHOTO FILM CO., LTD. (JP) 2007-02-06 US disclosed
US-6365068-B1 IN SOLVENT HYDRO-QUEBEC (CA) 2002-04-02 US disclosed
US-6171522-B1 Heterocyclic aromatic anion salts, and their uses as ionic conducting materials Hydro-Qu{acute over (e)}bec (CA) 2001-01-09 US disclosed
WO-1998029396-A1 HETEROCYCLIC AROMATIC ANION SALTS, AND THEIR USES AS IONIC CONDUCTING MATERIALS HYDRO-QUEBEC (CA) 1998-07-09 WO disclosed
EP-0850932-A1 Salts of heterocyclic anions and their uses as ionic conductive materials CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) 1998-07-01 EP disclosed
EP-0611109-A1 Silver halide light-sensitive photographic material KONICA CORPORATION (JP) 1994-08-17 EP disclosed
US-4831096-A VARYING THERMAL STABILITIES PENNWALT CORPORATION (US) 1989-05-16 US disclosed
US-4604455-A REACTING TWO PRIMARY AMINES WITH SULFURYL CHLORIDE, OXIDIZING MIXTURE OF SULFAMIDE PRODUCTS PENNWALT CORPORATION (US) 1986-08-05 US disclosed
US-4544742-A PROMOTERS FOR DENTAL PEROXIDIC POLYMERIZATIONS SCHMITT WERNER (DE) 1985-10-01 US disclosed
EP-0059451-B1 1,2,6-THIADIAZINE-3,5-DIONE-1,1 DIOXIDES AND THEIR USE ESPE Fabrik Pharmazeutischer Präparate GmbH (DE) 1985-07-31 EP disclosed
US-4443587-A FOR ADDITION POLYMERS ABITZ, MORF, GRITSCHNEDER (DE) 1984-04-17 US disclosed
EP-0059451-A1 1,2,6-Thiadiazine-3,5-dione-1,1 dioxides and their use ESPE Fabrik Pharmazeutischer Präparate GmbH (DE) 1982-09-08 EP disclosed
US-4146550-A REACTION OF CARBAMIC ACID CHLORIDE WITH ACTIVE HYDROGEN COMPOUND, DECOMPOSITION BAYER AKTIENGESELLSCHAFT (DE) 1979-03-27 US disclosed