SCHEMBL932564

SCHEMBL932564

C[C@@H](C(=O)O)N1C(=O)C=CC1=O

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CSNK2A2 P19784 1/20 0.48
CSNK2B P67870 1/20 0.48
CSNK2A1 P68400 1/20 0.48
KMT2A Q03164 3/20 0.44
MEN1 O00255 2/20 0.44
KDM4E B2RXH2 3/20 0.42
GAA P10253 1/20 0.42
CASP1 P29466 1/20 0.42
CASP7 P55210 1/20 0.42
LMNA P02545 2/20 0.40
HSD17B10 Q99714 1/20 0.39
ALDH1A1 P00352 1/20 0.38
DDAH1 O94760 1/20 0.38
NSD2 O96028 1/20 0.38
G6PD P11413 1/20 0.38
KEAP1 Q14145 1/20 0.38
NFE2L2 Q16236 1/20 0.38
GSK3A P49840 1/20 0.36
GSK3B P49841 1/20 0.36
MGLL Q99685 1/20 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
SCHEMBL15318993 1.00 CSNK2A2 (0.48) CSNK2A2CSNK2BCSNK2A1KMT2AMEN1
SCHEMBL43717 1.00 CSNK2A2 (0.48) CSNK2A2CSNK2BCSNK2A1KMT2AMEN1
SCHEMBL28981240 0.98 CSNK2A2 (0.47) CSNK2A2CSNK2BCSNK2A1KMT2AMEN1
Mercaptopropionic Acid SCHEMBL4955336 0.85 PTGS1 (0.39) CSNK2A2CSNK2BCSNK2A1KMT2AMEN1
SCHEMBL6047333 0.85 KMT2A (0.42) CSNK2A2CSNK2BCSNK2A1KMT2AMEN1
SCHEMBL15391718 0.82 PTGS1 (0.51) CSNK2A2CSNK2BCSNK2A1KDM4ELMNA
SCHEMBL22241544 0.81 LMNA (0.36) CSNK2A2CSNK2BCSNK2A1KMT2AMEN1
SCHEMBL2611102 0.81 LMNA (0.36) CSNK2A2CSNK2BCSNK2A1KMT2AMEN1
SCHEMBL28844372 0.80 TSHR (0.39) CSNK2A2CSNK2BCSNK2A1KMT2AMEN1
SCHEMBL321357 0.79 LMNA (0.35) CSNK2A2CSNK2BCSNK2A1KMT2AMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240208987-A1 EXATECAN-DERIVED ADC LINKER-PAYLOADS, PHARMACEUTICAL COMPOSITIONS, AND USES THEREOF MERCK SHARP & DOHME LLC (US) 2024-06-27 US disclosed
WO-2024091437-A1 EXATECAN-DERIVED ADC LINKER-PAYLOADS, PHARMACEUTICAL COMPOSITIONS, AND USES THEREOF MERCK SHARP & DOHME LLC (US) 2024-05-02 WO disclosed
EP-2451839-B1 METHOD FOR THE PRODUCTION OF VARIABLE DOMAINS ABLYNX NV (BE) 2020-04-22 EP disclosed
US-9150640-B2 Method for the production of variable domains ABLYNX N.V. (BE) 2015-10-06 US disclosed
US-9012567-B2 Supramolecular polymers and compositions containing said polymers RHODIA OPERATIONS (FR) 2015-04-21 US disclosed
US-20150023963-A1 METHOD FOR THE PRODUCTION OF VARIABLE DOMAINS ABLYNX N.V. (BE) 2015-01-22 US disclosed
WO-2015000585-A1 MUTEINS OF CYTOKINES OF THE GAMMA-CHAIN RECEPTOR FAMILY CONJUGATED TO A NON-PROTEIN GROUP SEBALD WALTER (DE) 2015-01-08 WO disclosed
US-20140073778-A9 CONJUGATES COMPRISING HYDROXYALKYL STARCH AND A CYTOTOXIC AGENT AND PROCESS FOR THEIR PREPARATION FRESENIUS KABI DEUTSCHLAND GMBH (DE) 2014-03-13 US disclosed
US-20130184454-A1 CONJUGATES COMPRISING HYDROXYALKYL STARCH AND A CYTOTOXIC AGENT AND PROCESS FOR THEIR PREPARATION FRESENIUS KABI DEUTSCHLAND GMBH (DE) 2013-07-18 US disclosed
EP-2524229-A1 METHOD FOR PREPARING POLYBIOTINYLATED COMPOUNDS Biomérieux (FR) 2012-11-21 EP disclosed
WO-2011086321-A1 METHOD FOR PREPARING POLYBIOTINYLATED COMPOUNDS bioMérieux (FR) 2011-07-21 WO disclosed
WO-2011003622-A1 METHOD FOR THE PRODUCTION OF VARIABLE DOMAINS ABLYNX N.V. (BE) 2011-01-13 WO disclosed
US-5773271-A Compounds from biopolymers and effector substances which are linked via optically active amino acid derivatives, processes for the preparation thereof and the use thereof BEHRING DIAGNOSTICS GMBH (DE) 1998-06-30 US disclosed
US-5744315-A Compounds from biopolymers and effector substances which are linked via optically active amino acid derivatives, processes for the preparation thereof and the use thereof BEHRING DIAGNOSTICS GMBH (DE) 1998-04-28 US disclosed
US-5484722-A Biopolymer and effector substance conjugates, process for the preparation thereof and their use BEHRINGWERKE AKTIENGESELLSCHAFT (DE) 1996-01-16 US disclosed
US-5321142-A Compounds from biopolymers and effector substances which are linked via optically active amino acid derivatives, processes for the preparation thereof and the use thereof BEHRINGWERKE AKTIENGESELLSCHAFT (DE) 1994-06-14 US disclosed
US-5030620-A Anticarcinogenic and antitumor agents OMNICHEM (BE) 1991-07-09 US disclosed
US-4828831-A ANTICANCER OMNICHEM (BE) 1989-05-09 US disclosed
EP-0308983-A2 NMR imaging with Mn(II) coordination compositions SALUTAR, INC. (US) 1989-03-29 EP disclosed
EP-0232693-A2 Conjugates of vinblastine and its derivatives, process for their preparation and pharmaceutical compositions containing them LA REGION WALLONNE (BE) 1987-08-19 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-20240208987-A1 EXATECAN-DERIVED ADC LINKER-PAYLOADS, PHARMACEUTICAL COMPOSITIONS, AND USES THEREOF ADCY3, ADCY8, ADCY7 CSNK2A2 3074/4885CSNK2B 3290/4885CSNK2A1 3440/4885

“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.