SCHEMBL1492162

SCHEMBL1492162

NCC(=O)NCCS(=O)(=O)O

nearest known ligand 0.44

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.44
SLC6A6 P31641 1/20 0.44
CYP2C19 P33261 1/20 0.44
BLM P54132 1/20 0.44
CA2 P00918 4/20 0.43
CA1 P00915 3/20 0.43
APP P05067 1/20 0.41
CYP2D6 P10635 1/20 0.35
MEN1 O00255 1/20 0.34
KMT2A Q03164 1/20 0.34
ALDH1A1 P00352 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.34
L3MBTL1 Q9Y468 1/20 0.34
MMP2 P08253 1/20 0.33
PTGS1 P23219 1/20 0.33
PDE4A P27815 1/20 0.33
AOC3 Q16853 1/20 0.33
CACNA1G O43497 1/20 0.32
EPHX2 P34913 1/20 0.32

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
SCHEMBL12380917 0.92 CA2 (0.39) LMNASLC6A6CYP2C19BLMCA2
SCHEMBL13944642 0.87 APP (0.48) LMNASLC6A6CYP2C19BLMCA2
SCHEMBL4183162 0.83 LMNA (0.46) LMNASLC6A6CYP2C19BLMCA2
SCHEMBL6913359 0.81 LMNA (0.44) LMNASLC6A6CYP2C19BLMCA2
SCHEMBL15808676 0.80 CA2 (0.42) LMNACA2CA1MEN1KMT2A
SCHEMBL7531907 0.80 MEN1 (0.38) LMNASLC6A6CYP2C19BLMCA2
SCHEMBL10886005 0.79 APP (0.50) LMNASLC6A6CYP2C19BLMCA2
SCHEMBL23929057 0.79 ACP1 (0.38) LMNASLC6A6CYP2C19BLMAPP
SCHEMBL4809608 0.79 ALDH1A1 (0.36) LMNASLC6A6CYP2C19BLMAPP
SCHEMBL30407466 0.79 L3MBTL1 (0.47) LMNASLC6A6CYP2C19BLMCYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0618235-B1 Process for the synthesis of semisynthetic glycosaminoglycans containing alpha-L-galacturonic acid substituted with nucleophilic radicals in position 3 ALFA WASSERMANN SPA (IT) 1997-07-23 EP claimed
EP-0565863-B1 Semi-synthetic glycosaminoglycans with heparin or heparan structure of alpha-L-iduronic-2-0-sulfate acid modified in position 2 ALFA WASSERMANN SPA (IT) 1997-06-18 EP claimed
EP-0565862-B1 Semi-synthetic glycosaminoglycans containing alpha-L-galacturonic acid substituted with nucleophilic radicals in position 3 ALFA WASSERMANN SPA (IT) 1997-06-18 EP claimed
EP-0618234-B1 Process for the synthesis of semisynthetic glycosaminoglycans with heparin or heparan structure modified in position 2 of the alpha-L-iduronic-2-0-sulfate acid ALFA WASSERMANN SPA (IT) 1997-06-04 EP claimed
EP-0467856-B1 Aminoalkanesulfonic acid derivatives and pharmaceutical compositions for use in preventing or treating heart diseases NIPPON ZOKI PHARMACEUTICAL CO (JP) 1997-03-19 EP claimed
US-5430133-A Semi-synthetic glycosaminoglycans with heparin or heparan structure of α-L-iduronic-2-O-sulfate acid modified in position 2 ALFA WASSERMANN S.P.A. (IT) 1995-07-04 US claimed
US-5410039-A Process for the synthesis of glycosaminoglycans containing α-L-galacturonic acid substituted with nucleophilic groups in position 3 ALFA WASSERMANN S.P.A. (IT) 1995-04-25 US claimed
US-5405949-A Process for the synthesis of glycosaminoglycans with heparin or heparan structure modified in position 2 of the α-L-iduronic-2-O-sulfate acid ALFA WASSERNANN S.P.A. (IT) 1995-04-11 US claimed
EP-0618235-A1 Process for the synthesis of semisynthetic glycosaminoglycans containig alpha-L-galacturonic acid substituted with nucleophilic radicals in position 3 ALFA WASSERMANN S.p.A. (IT) 1994-10-05 EP claimed
EP-0618234-A1 Process for the synthesis of semisynthetic glycosaminoglycans with heparin or heparan structure modified in position 2 of the alpha-L-iduronic-2-0-sulfate acid ALFA WASSERMANN S.p.A. (IT) 1994-10-05 EP claimed
EP-0565863-A2 Semi-synthetic glycosaminoglycans with heparin or heparan structure of alpha-L-iduronic-2-0-sulfate acid modified in position 2 ALFA WASSERMANN S.p.A. (IT) 1993-10-20 EP claimed
EP-0565862-A2 Semi-synthetic glycosaminoglycans containing alpha-L-galacturonic acid substituted with nucleophilic radicals in position 3 ALFA WASSERMANN S.p.A. (IT) 1993-10-20 EP claimed
EP-0467856-A2 Aminoalkanesulfonic acid derivatives and pharmaceutical compositions for use in preventing or treating heart diseases NIPPON ZOKI PHARMACEUTICAL CO. LTD. (JP) 1992-01-22 EP claimed
JP-4077423-A None JP disclosed
EP-2470553-B1 POLYHYDROXYLATED BILE ACIDS FOR TREATMENT OF BILIARY DISORDERS QING BILE THERAPEUTICS INC (CA) 2024-06-19 EP disclosed
US-11980645-B2 Bile acids and use in disease treatment THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2024-05-14 US disclosed
EP-0565863-A2 Semi-synthetic glycosaminoglycans with heparin or heparan structure of alpha-L-iduronic-2-0-sulfate acid modified in position 2 ALFA WASSERMANN S.p.A. (IT) 1993-10-20 EP disclosed
EP-0565862-A2 Semi-synthetic glycosaminoglycans containing alpha-L-galacturonic acid substituted with nucleophilic radicals in position 3 ALFA WASSERMANN S.p.A. (IT) 1993-10-20 EP disclosed
JP-H0477423-A THERAPEUTIC AGENT FOR HEART DISEASE NIPPON ZOKI PHARMACEUT CO LTD 1992-03-11 JP disclosed
EP-0472205-A1 Assays using a soluble fibrin-like monomer New York Blood Center, Inc. (US) 1992-02-26 EP 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 (1 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-11980645-B2 Bile acids and use in disease treatment SLC10A2, NR1H4, GPBAR1 LMNA 2285/4885SLC6A6 428/4885CYP2C19 117/4885

“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.