Sulfuric Acid

Sulfuric Acid

SCHEMBL7955346

CCN(CC)c1ccc(N)c(C)c1.O=S(=O)(O)O

nearest known ligand 0.80

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Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Sulfuric Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
S100B P04271 1/20 0.80
ALDH1A1 P00352 8/20 0.46
L3MBTL1 Q9Y468 6/20 0.46
MEN1 O00255 3/20 0.46
KMT2A Q03164 3/20 0.46
HPGD P15428 3/20 0.46
CYP2C19 P33261 3/20 0.46
HSP90AA1 P07900 1/20 0.46
CYP2C9 P11712 1/20 0.46
MAPK1 P28482 6/20 0.44
GFER P55789 6/20 0.44
CYP3A4 P08684 3/20 0.44
PSMD14 O00487 1/20 0.44
TSHR P16473 1/20 0.44
RECQL P46063 1/20 0.44
TDP1 Q9NUW8 1/20 0.44
POLB P06746 2/20 0.43
GRK2 P25098 1/20 0.43
DNMT1 P26358 1/20 0.43
CTDSP1 Q9GZU7 1/20 0.43

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
Methanesulfonamide SCHEMBL6897381 0.95 S100B (0.73) S100BALDH1A1L3MBTL1MEN1KMT2A
Methanesulfonamide SCHEMBL793229 0.90 S100B (0.80) S100BALDH1A1L3MBTL1MEN1KMT2A
Sulfuric Acid SCHEMBL2140481 0.90 S100B (0.64) S100BALDH1A1L3MBTL1MEN1KMT2A
Sulfuric Acid SCHEMBL10371487 0.90 S100B (0.64) S100BALDH1A1L3MBTL1MEN1KMT2A
Sulfuric Acid SCHEMBL9566805 0.90 S100B (0.64) S100BALDH1A1L3MBTL1MEN1KMT2A
Sulfuric Acid SCHEMBL10945925 0.90 S100B (0.64) S100BALDH1A1L3MBTL1MEN1KMT2A
Sulfuric Acid SCHEMBL10582678 0.90 S100B (0.64) S100BALDH1A1L3MBTL1MEN1KMT2A
SCHEMBL34104 0.89 S100B (1.00) S100BALDH1A1L3MBTL1MEN1KMT2A
SCHEMBL29350181 0.89 S100B (1.00) S100BALDH1A1L3MBTL1MEN1KMT2A
Sulfuric Acid SCHEMBL9131658 0.88 S100B (0.62) S100BALDH1A1L3MBTL1MEN1KMT2A

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 28 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6265600-B1 REACTING IMIDATE COMPOUND TO CONDENSATION REACTION IN NITROGEN ATOMOSPHERE IN PRESENCE OF BASE AND ACTIVATED METHYLENE COMPOUND TO FORM ACTIVATED PROPENE COMPOUND EASTMAN KODAK COMPANY 2001-07-24 US disclosed
US-5776669-A Phenol substituted pyrazolo 1, 5-a benzimidazole couplers EASTMAN KODAK COMPANY (US) 1998-07-07 US disclosed
US-5460927-A Reacting a propene compound with nucleophilic aniline derivatives; used in silver halide imaging system EASTMAN KODAK COMPANY (US) 1995-10-24 US disclosed
EP-0565531-B1 ACTIVATED PROPENES AS COLOUR COUPLERS KODAK LTD (GB) 1995-09-06 EP disclosed
US-5443945-A Magenta photographic couplers EASTMAN KODAK COMPANY (US) 1995-08-22 US disclosed
EP-0592509-B1 ACTIVATED PROPENES AS COLOUR COUPLERS AND A METHOD FOR THEIR PRODUCTION KODAK LTD (GB) 1995-06-14 EP disclosed
EP-0358186-B1 Photographic silver halide material and process EASTMAN KODAK CO (US) 1994-08-24 EP disclosed
EP-0594615-A1 PHENOL SUBSTITUTED PYRAZOLO 1,5-a]BENZIMIDAZOLE COUPLERS KODAK LIMITED (GB) 1994-05-04 EP disclosed
EP-0592509-A1 ACTIVATED PROPENES AS COLOUR COUPLERS AND A METHOD FOR THEIR PRODUCTION. KODAK LTD (GB) 1994-04-20 EP disclosed
EP-0213710-B1 Method of processing silver halide color photographic material KONISHIROKU PHOTO IND (JP) 1994-01-12 EP disclosed
WO-1992000299-A1 PHENOL SUBSTITUTED PYRAZOLO[1,5-a]BENZIMIDAZOLE COUPLERS EASTMAN KODAK COMPANY (US) 1992-01-09 WO disclosed
EP-0398750-A2 Tone controlling compounds EASTMAN KODAK COMPANY (US) 1990-11-22 EP disclosed
EP-0358186-A2 Photographic silver halide material and process EASTMAN KODAK COMPANY (US) 1990-03-14 EP disclosed
US-4908300-A Developing imagewise exposed silver halide photographic material, maintaining dry thickness, bleach-fixing with organic acid ferric complex KONISHIROKU PHOTO INDUSTRY CO., LTD. (JP) 1990-03-13 US disclosed
US-4908304-A Silver halide emulsion contains hydroxytetrazaindene compound and electron beam hardenable resin KONISHIROKU PHOTO INDUSTRY CO., LTD. (JP) 1990-03-13 US disclosed
US-4748105-A Rapid bleach fixing of a silver halide color photographic light-sensitive material using an organic acid ferric complex KONISIROKU PHOTO INDUSTRY COMPANY, LTD. (JP) 1988-05-31 US disclosed
US-4707434-A Color image forming method comprising processing with a bleach-fixing solution KONISHIROKU PHOTO INDUSTRY CO., LTD. (JP) 1987-11-17 US disclosed
EP-0213710-A2 Method of processing silver halide color photographic material KONICA CORPORATION (JP) 1987-03-11 EP disclosed
EP-0175366-A2 Silver halide photographic light-sensitive material KONICA CORPORATION (JP) 1986-03-26 EP disclosed
EP-0173540-A2 Color image forming method KONICA CORPORATION (JP) 1986-03-05 EP disclosed