SCHEMBL969243

SCHEMBL969243

CCCCCCCCCCCCc1ccc(S(=O)(=O)N=[N+]=[N-])cc1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 3/20 0.55
SMN1; SMN2 Q16637 2/20 0.49
ENPP2 Q13822 1/20 0.46
CA12 O43570 1/20 0.46
CA1 P00915 1/20 0.46
CA9 Q16790 1/20 0.46
ESR1 P03372 2/20 0.45
ADRA2A P08913 2/20 0.45
ADORA3 P0DMS8 2/20 0.45
TACR2 P21452 2/20 0.45
SLC6A2 P23975 2/20 0.45
SLC6A4 P31645 2/20 0.45
SLC6A3 Q01959 2/20 0.45
LMNA P02545 2/20 0.45
KDM4E B2RXH2 2/20 0.45
ALDH1A1 P00352 1/20 0.45
SHBG P04278 1/20 0.45
TP53 P04637 1/20 0.45
CYP3A4 P08684 1/20 0.45
HSPD1 P10809 1/20 0.45

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
SCHEMBL28459415 1.00 CA2 (0.55) CA2SMN1; SMN2ENPP2CA12CA1
SCHEMBL11595972 0.94 CA2 (0.56) CA2SMN1; SMN2CA12CA1CA9
SCHEMBL6014622 0.92 CA2 (0.45) CA2SMN1; SMN2ENPP2CA12CA1
SCHEMBL31594518 0.87 CA2 (0.53) CA2SMN1; SMN2CA9LMNAALDH1A1
SCHEMBL17704474 0.84 MAOB (0.42) CA2CA12CA1ALDH1A1TP53
SCHEMBL18878046 0.82 NR1I2 (0.49) CA2SMN1; SMN2ENPP2CA12CA1
SCHEMBL11594759 0.80 CA2 (0.50) CA2SMN1; SMN2LMNAKDM4EALDH1A1
SCHEMBL14798581 0.79 CA2 (0.38) CA2SMN1; SMN2CA12CA1CA9
SCHEMBL2637873 0.79 KCNH2 (0.49) CA2ENPP2ESR1ADRA2AADORA3
SCHEMBL14798250 0.78 CA2 (0.37) CA2SMN1; SMN2CA12CA1CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117603133-A Application of quaternary ammonium salt in continuous flow Curtius rearrangement reaction 瑞博(苏州)制药有限公司 2024-02-27 CN claimed
CN-115625956-B PE multilayer barrier composite film and preparation method thereof 江苏欧晟新材料科技有限公司 2023-10-10 CN claimed
CN-115625956-A PE multilayer barrier composite film and preparation method thereof 江苏欧晟新材料科技有限公司 2023-01-20 CN claimed
CN-113740526-A Modified sealing agent and preparation method thereof 广西康柏莱科技有限公司 2021-12-03 CN claimed
CN-109705106-B Preparation method of tannin derivative 吉首大学 2021-10-19 CN claimed
EP-2344515-B9 METHOD AND INTERMEDIATES FOR PREPARING 2-ALKOXY AND 2-ARYLOXY ESTROGEN COMPOUNDS NAXOSPHARMA S R L (IT) 2013-06-26 EP claimed
EP-2344515-B1 METHOD AND INTERMEDIATES FOR PREPARING 2-ALKOXY AND 2-ARYLOXY ESTROGEN COMPOUNDS NAXOSPHARMA S R L (IT) 2013-02-13 EP claimed
EP-2344515-A1 METHOD AND INTERMEDIATES FOR PREPARING 2-ALKOXY AND 2-ARYLOXY ESTROGEN COMPOUNDS Naxospharma S.R.L. (IT) 2011-07-20 EP claimed
US-7901904-B2 Method and intermediates for preparing 2-alkoxy and 2-aryloxy estrogen compounds NAXOSPHARMA S.R.L. (IT) 2011-03-08 US claimed
WO-2010043506-A1 METHOD AND INTERMEDIATES FOR PREPARING 2-ALKOXY AND 2-ARYLOXY ESTROGEN COMPOUNDS NAXOSPHARMA S.R.L. (IT) 2010-04-22 WO claimed
US-20080214409-A1 Substrate structure, oligomer probe array and methods for producing the same SAMSUNG ELECTRONICS CO., LTD. 2008-09-04 US claimed
EP-1958690-A1 Substrate structure, oligomer probe array and methods for producing the same Samsung Electronics Co., Ltd. (KR) 2008-08-20 EP claimed
EP-0965068-A1 PHOTOSENSITIVE QUINOLONE COMPOUNDS AND A PROCESS OF PREPARATION CLARIANT INTERNATIONAL LTD. (CH) 1999-12-22 EP claimed
WO-1998040790-A1 PHOTOSENSITIVE QUINOLONE COMPOUNDS AND A PROCESS OF PREPARATION CLARIANT INTERNATIONAL (CH) 1998-09-17 WO claimed
EP-0345999-A1 Process for intermediates to 1-carba(1-dethia)-3-cephem-4-carboxylic acids ELI LILLY AND COMPANY (US) 1989-12-13 EP claimed
EP-0160218-B1 PROCESS FOR PREPARING C8 -C24 ALKYLBENZENE SULFONYLAZIDES MERCK & CO. INC. (US) 1987-10-21 EP claimed
US-4616084-A Process for the preparation of 7-acylamino-3-hydroxy-cephem-4-carboxylic acids and 7-acylamino-3-hydroxy-1-dethia-1-oxacephem-4-carboxylic acids BAYER AKTIENGESELLSCHAFT (DE) 1986-10-07 US claimed
EP-0160218-A1 Process for preparing C8 -C24 alkylbenzene sulfonylazides MERCK & CO. INC. (US) 1985-11-06 EP claimed
EP-0133670-A2 Process for the preparation of 7-acylamino-3-hydroxy-cephem-4-carboxylic acids and 7-acylamino-3-hydroxy-1-dethia-1-oxacephem-4-carboxylic acids BAYER AG (DE) 1985-03-06 EP claimed
US-4284575-A Substituted benzenesulfonylazides MERCK & CO., INC. (US) 1981-08-18 US claimed