SCHEMBL1331630

SCHEMBL1331630

CC1(C)OB(c2ccc(NS(=O)(=O)c3ccccc3)cc2)OC1(C)C

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA1 P00915 8/20 0.64
CA2 P00918 8/20 0.64
CA9 Q16790 8/20 0.64
CA12 O43570 3/20 0.64
CA3 P07451 1/20 0.64
CA4 P22748 1/20 0.64
CA6 P23280 1/20 0.64
CA5A P35218 1/20 0.64
CA7 P43166 1/20 0.64
CA14 Q9ULX7 1/20 0.64
CA5B Q9Y2D0 1/20 0.64
MEN1 O00255 3/20 0.56
KMT2A Q03164 3/20 0.56
ALDH1A1 P00352 1/20 0.56
PKM P14618 1/20 0.56
KEAP1 Q14145 2/20 0.54
IL1RN P18510 1/20 0.54
ERAP1 Q9NZ08 1/20 0.54
LPL P06858 1/20 0.53
LIPG Q9Y5X9 1/20 0.53

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
SCHEMBL20995717 0.94 CA9 (0.62) CA1CA2CA9CA12CA3
SCHEMBL4909467 0.87 CA1 (0.65) CA1CA2CA9CA12CA3
SCHEMBL18395483 0.86 CA1 (0.63) CA1CA2CA9CA12CA3
SCHEMBL15504644 0.86 CA1 (0.63) CA1CA2CA9CA12CA3
SCHEMBL11894843 0.85 HTR6 (0.51) CA1CA2CA9CA12CA3
SCHEMBL5674321 0.83 CA1 (0.61) CA1CA2CA9CA12CA3
SCHEMBL3262774 0.82 CA1 (0.60) CA1CA2CA9CA12CA3
SCHEMBL790984 0.81 ALPL (0.48) CA1CA2CA9CA12CA3
SCHEMBL15091914 0.81 CA1 (0.58) CA1CA2CA9CA12CA3
SCHEMBL31438923 0.81 CA1 (0.58) CA1CA2CA9CA12CA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119725741-A Electrolyte for lithium iron manganese phosphate system battery and lithium ion battery 安徽得壹能源科技有限公司 2025-03-28 CN disclosed
EP-2569301-A1 INDAZOLE INHIBITORS OF KINASE Abbvie Inc. (US) 2013-03-20 EP disclosed
US-8293738-B2 Indazole inhibitors of kinase ABBOTT LABORATORIES (US) 2012-10-23 US disclosed
EP-2487175-A1 PHARMACEUTICAL PRODUCT CONTAINING AROMATIC HETEROCYCLIC COMPOUND Kyowa Hakko Kirin Co., Ltd. (JP) 2012-08-15 EP disclosed
US-20120196854-A1 PHARMACEUTICAL COMPOSITION COMPRISING AROMATIC HETEROCYCLIC COMPOUND KYOWA HAKKO KIRIN CO., LTD. (JP) 2012-08-02 US disclosed
US-20110281868-A1 INDAZOLE INHIBITORS OF KINASE ABBOTT LABORATORIES (US) 2011-11-17 US disclosed
WO-2011143430-A1 INDAZOLE INHIBITORS OF KINASE ABBOTT LABORATORIES (US) 2011-11-17 WO disclosed
US-8003655-B2 Dysregulated vascular growth diseases; tyrosine kinase with immunoglobulin and epidermal growth factor homology domain inhibitors BAYER SCHERING PHARMA AG (DE) 2011-08-23 US disclosed
US-8003655-B2 Dysregulated vascular growth diseases; tyrosine kinase with immunoglobulin and epidermal growth factor homology domain inhibitors BAYER SCHERING PHARMA AG (DE) 2011-08-23 US disclosed
US-8003655-B2 Dysregulated vascular growth diseases; tyrosine kinase with immunoglobulin and epidermal growth factor homology domain inhibitors BAYER SCHERING PHARMA AG (DE) 2011-08-23 US disclosed
EP-2046758-A1 SUBSTITUTED SULPHOXIMINES AS TIE2 INHIBITORS AND SALTS THEREOF, PHARMACEUTICAL COMPOSITIONS COMPRISING SAME, METHODS OF PREPARING SAME AND USES OF SAME Bayer Schering Pharma Aktiengesellschaft (DE) 2009-04-15 EP disclosed
US-7494995-B2 Phenylpyridylpiperazine compounds LES LABORATOIRES SERVIER (FR) 2009-02-24 US disclosed
US-20080064696-A1 SUBSTITUTED SULPHOXIMINES AS TIE2 INHIBITORS AND SALTS THEREOF, PHARMACEUTICAL COMPOSITIONS COMPRISING SAME, METHODS OF PREPARING SAME AND USES OF SAME BAYER INTELLECTUAL PROPERTY GMBH (DE) 2008-03-13 US disclosed
US-20080064696-A1 SUBSTITUTED SULPHOXIMINES AS TIE2 INHIBITORS AND SALTS THEREOF, PHARMACEUTICAL COMPOSITIONS COMPRISING SAME, METHODS OF PREPARING SAME AND USES OF SAME BAYER INTELLECTUAL PROPERTY GMBH (DE) 2008-03-13 US disclosed
US-20080064696-A1 SUBSTITUTED SULPHOXIMINES AS TIE2 INHIBITORS AND SALTS THEREOF, PHARMACEUTICAL COMPOSITIONS COMPRISING SAME, METHODS OF PREPARING SAME AND USES OF SAME BAYER INTELLECTUAL PROPERTY GMBH (DE) 2008-03-13 US disclosed
WO-2008006560-A1 SUBSTITUTED SULPHOXIMINES AS TIE2 INHIBITORS AND SALTS THEREOF, PHARMACEUTICAL COMPOSITIONS COMPRISING SAME, METHODS OF PREPARING SAME AND USES OF SAME BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2008-01-17 WO disclosed
EP-1878726-A1 Substituted sulphoximines as Tie2 inhibitors and salts thereof, pharmaceutical compositions comprising the same, methods of preparing the same and uses of the same Bayer Schering Pharma Aktiengesellschaft (DE) 2008-01-16 EP disclosed
US-20060258671-A1 Phenylpyridylpiperazine compounds LES LABORATORIES SERVIER (FR) 2006-11-16 US disclosed
EP-1721896-A1 Phenylpyridinylpiperazin derivatives, the process to make them and the compositions containing them Les Laboratoires Servier (FR) 2006-11-15 EP disclosed
US-20060194823-A1 Sulfonamido-macrocycles as Tie2 inhibitors and the salts thereof, a pharmaceutical composition comprising these compounds, the method of preparing and the use thereof BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2006-08-31 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20060194823-A1 Sulfonamido-macrocycles as Tie2 inhibitors and the salts thereof, a pharmaceutical composition comprising these compounds, the method of preparing and the use thereof TEK, TIE1, KDR CA1 3872/4885CA2 1503/4885CA9 2323/4885
US-20060258671-A1 Phenylpyridylpiperazine compounds HRH4, HRH3, HRH2 CA1 3410/4885CA2 2295/4885CA9 4510/4885
US-20110281868-A1 INDAZOLE INHIBITORS OF KINASE AURKA, AURKC, AURKB CA1 3477/4885CA2 1064/4885CA9 2444/4885
US-20120196854-A1 PHARMACEUTICAL COMPOSITION COMPRISING AROMATIC HETEROCYCLIC COMPOUND CYP2C18, H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, CYP2B6 CA1 3327/4885CA2 2053/4885CA9 2295/4885
US-20080064696-A1 SUBSTITUTED SULPHOXIMINES AS TIE2 INHIBITORS AND SALTS THEREOF, PHARMACEUTICAL COMPOSITIONS COMPRISING SAME, METHODS OF PREPARING SAME AND USES OF SAME TIE1, KDR, TEK CA1 4147/4885CA2 1369/4885CA9 2845/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.