SCHEMBL1507229

SCHEMBL1507229

C[N+](C)(C)Cc1ccccc1.C[N+](C)(C)Cc1ccccc1.O=S(=O)([O-])OOS(=O)(=O)[O-]

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.61
KDM4E B2RXH2 1/20 0.61
TDP1 Q9NUW8 1/20 0.61
CHRNB2 P17787 1/20 0.39
CHRNA4 P43681 1/20 0.39
CA9 Q16790 5/20 0.38
CA12 O43570 4/20 0.38
CA1 P00915 4/20 0.38
CA2 P00918 4/20 0.38
L3MBTL1 Q9Y468 2/20 0.38
CA7 P43166 2/20 0.38
CA4 P22748 1/20 0.38
CA5A P35218 1/20 0.38
CA5B Q9Y2D0 1/20 0.38
BCHE P06276 1/20 0.38
ACHE P22303 1/20 0.38
CYP1A2 P05177 1/20 0.38
CYP3A4 P08684 1/20 0.38
ATM Q13315 1/20 0.38
POLB P06746 2/20 0.36

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
SCHEMBL6621494 0.92 ALDH1A1 (0.52) ALDH1A1KDM4ETDP1CHRNB2CHRNA4
SCHEMBL1027231 0.89 ALDH1A1 (0.61) ALDH1A1KDM4ETDP1CHRNB2CHRNA4
Sulfuric Acid SCHEMBL229799 0.88 KDM4E (0.71) ALDH1A1KDM4ETDP1CHRNB2CHRNA4
Sulfuric Acid SCHEMBL7637635 0.86 KDM4E (0.68) ALDH1A1KDM4ETDP1CHRNB2CHRNA4
Sulfuric Acid SCHEMBL2243812 0.86 KDM4E (0.68) ALDH1A1KDM4ETDP1CHRNB2CHRNA4
SCHEMBL332134 0.86 KDM4E (0.68) ALDH1A1KDM4ETDP1CHRNB2CHRNA4
SCHEMBL6620666 0.85 KDM4E (0.39) ALDH1A1KDM4ETDP1CA9CA12
Thiosulfuric Acid SCHEMBL8424190 0.85 KDM4E (0.65) ALDH1A1KDM4ETDP1CHRNB2CHRNA4
SCHEMBL330944 0.85 KDM4E (0.65) ALDH1A1KDM4ETDP1CHRNB2CHRNA4
Sulfuric Acid SCHEMBL229801 0.85 KDM4E (0.65) ALDH1A1KDM4ETDP1CHRNB2CHRNA4

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 12 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8026200-B2 Low pH mixtures for the removal of high density implanted resist ADVANCED TECHNOLOGY MATERIALS, INC. (US) 2011-09-27 US claimed
EP-2288965-A2 LOW PH MIXTURES FOR THE REMOVAL OF HIGH DENSITY IMPLANTED RESIST Advanced Technology Materials, Inc. (US) 2011-03-02 EP claimed
US-20090281016-A1 LOW pH MIXTURES FOR THE REMOVAL OF HIGH DENSITY IMPLANTED RESIST ADVANCED TECHNOLOGY MATERIALS, INC. (US) 2009-11-12 US claimed
WO-2009135102-A2 LOW PH MIXTURES FOR THE REMOVAL OF HIGH DENSITY IMPLANTED RESIST ADVANCED TECHNOLOGY MATERIALS, INC. (US) 2009-11-05 WO claimed
US-8026200-B2 Low pH mixtures for the removal of high density implanted resist ADVANCED TECHNOLOGY MATERIALS, INC. (US) 2011-09-27 US disclosed
EP-2288965-A2 LOW PH MIXTURES FOR THE REMOVAL OF HIGH DENSITY IMPLANTED RESIST Advanced Technology Materials, Inc. (US) 2011-03-02 EP disclosed
US-20090281016-A1 LOW pH MIXTURES FOR THE REMOVAL OF HIGH DENSITY IMPLANTED RESIST ADVANCED TECHNOLOGY MATERIALS, INC. (US) 2009-11-12 US disclosed
WO-2009135102-A2 LOW PH MIXTURES FOR THE REMOVAL OF HIGH DENSITY IMPLANTED RESIST ADVANCED TECHNOLOGY MATERIALS, INC. (US) 2009-11-05 WO disclosed
EP-0985664-B1 Method of producing pyrrolidine derivatives TORAY FINECHEMICALS CO LTD (JP) 2004-03-31 EP disclosed
US-6479668-B1 Method of producing pyrrolidine derivatives TORAY INDUSTRIES, INC. (JP) 2002-11-12 US disclosed
US-6130338-A OXIDATING THE CORRESPONDING 3-PYRROLINE COMPOUND TO GIVE AN EPOXYPYRROLIDINE COMPOUND TORAY INDUSTRIES, INC. (JP) 2000-10-10 US disclosed
EP-0985664-A2 Method of producing pyrrolidine derivatives TORAY INDUSTRIES, INC. (JP) 2000-03-15 EP disclosed