SCHEMBL2129165

SCHEMBL2129165

NC(=O)c1cccc(CO)c1C(N)=O

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PARP1 P09874 5/20 0.46
MEN1 O00255 1/20 0.44
KMT2A Q03164 1/20 0.44
BCAT2 O15382 1/20 0.42
KDM4E B2RXH2 3/20 0.42
HPGD P15428 2/20 0.42
ALDH1A1 P00352 2/20 0.42
MAPT P10636 1/20 0.42
TSHR P16473 1/20 0.42
HSD17B10 Q99714 1/20 0.42
GAA P10253 2/20 0.40
LMNA P02545 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.40
METAP2 P50579 1/20 0.39
SIRT1 Q96EB6 1/20 0.39
AURKA O14965 2/20 0.39
RPS6KB1 P23443 2/20 0.39
KEAP1 Q14145 1/20 0.38
NFE2L2 Q16236 1/20 0.38
PDPK1 O15530 1/20 0.38

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
SCHEMBL6566956 0.84 PARP1 (0.47) PARP1MEN1KMT2ABCAT2KDM4E
SCHEMBL6075761 0.82 KDM4E (0.41) PARP1MEN1KMT2ABCAT2KDM4E
SCHEMBL619877 0.81 ALDH1A1 (0.52) PARP1MEN1KMT2ABCAT2KDM4E
SCHEMBL8652707 0.81 HMGB1 (0.54) PARP1MEN1KMT2ABCAT2KDM4E
SCHEMBL466296 0.80 KDM4E (0.54) PARP1BCAT2KDM4EHPGDALDH1A1
SCHEMBL5545298 0.80 PARP1 (0.46) PARP1MEN1KMT2ABCAT2KDM4E
SCHEMBL7325664 0.80 HMGB1 (0.49) PARP1MEN1KMT2ABCAT2KDM4E
SCHEMBL3483399 0.79 KDM4E (0.38) PARP1MEN1KMT2ABCAT2KDM4E
SCHEMBL1063004 0.79 BID (0.41) PARP1MEN1KMT2AKDM4EHPGD
SCHEMBL5545065 0.78 ALDH1A1 (0.47) MEN1KMT2AHPGDALDH1A1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-7186538-A None JP disclosed
US-20250340507-A1 METHODS FOR SYNTHESIZING SUBSTITUTED TETRACYCLINE COMPOUNDS PARATEK PHARM INNC (US) 2025-11-06 US disclosed
US-20170283368-A1 METHODS FOR SYNTHESIZING SUBSTITUTED TETRACYCLINE COMPOUNDS PARATEK PHARMACEUTICALS, INC. 2017-10-05 US disclosed
US-9522872-B2 Methods for synthesizing substituted tetracycline compounds PARATEK PHARMACEUTICALS, INC. (US) 2016-12-20 US disclosed
EP-2176216-B1 METHODS FOR SYNTHESIZING 9-SUBSTITUTED MINOCYCLINE PARATEK PHARM INNC (US) 2012-04-25 EP disclosed
EP-2192111-A2 Methods for synthesizing substituted tetracycline compounds Paratek Pharmaceuticals, Inc. (US) 2010-06-02 EP disclosed
EP-2176216-A1 METHODS FOR SYNTHESIZING SUBSTITUTED TETRACYCLINE COMPOUNDS Paratek Pharmaceuticals, Inc. (US) 2010-04-21 EP disclosed
US-20090156842-A1 Methods for synthesizing substituted tetracycline compounds PARATEK PHARMACEUTICALS, INC. 2009-06-18 US disclosed
WO-2009009042-A1 METHODS FOR SYNTHESIZING SUBSTITUTED TETRACYCLINE COMPOUNDS PARATEK PHARMACEUTICALS, INC. (US) 2009-01-15 WO disclosed
EP-1347968-A1 LFA-1 ANTAGONIST COMPOUNDS GENENTECH, INC. (US) 2003-10-01 EP disclosed
WO-2002059114-A9 LFA-1 ANTAGONIST COMPOUNDS GENENTECH INC (US) 2002-10-17 WO disclosed
WO-2002059114-A1 LFA-1 ANTAGONIST COMPOUNDS GENENTECH, INC. (US) 2002-08-01 WO disclosed
JP-H07186538-A OPTICAL RECORDING MATERIAL TOYO INK MFG CO LTD 1995-07-25 JP disclosed
EP-0073826-A1 RAPID SOLID PHASE SYNTHESIS OF OLIGONUCLEOTIDES USING PHOSPHORUS OXYCHLORIDE ACTIVATION BIORESEARCH INC. (US) 1983-03-16 EP disclosed
WO-1982003079-A1 RAPID SOLID PHASE SYNTHESIS OF OLIGONUCLEOTIDES USING PHOSPHORUS OXYCHLORIDE ACTIVATION BIORESEARCH INC (US) 1982-09-16 WO 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 (3 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-20090156842-A1 Methods for synthesizing substituted tetracycline compounds TET3, TET1, DHFR PARP1 2378/4885MEN1 2384/4885KMT2A 1153/4885
US-20250340507-A1 METHODS FOR SYNTHESIZING SUBSTITUTED TETRACYCLINE COMPOUNDS TET3, TET1, DHFR PARP1 2378/4885MEN1 2384/4885KMT2A 1153/4885
US-20170283368-A1 METHODS FOR SYNTHESIZING SUBSTITUTED TETRACYCLINE COMPOUNDS TET3, TET1, DHFR PARP1 2378/4885MEN1 2384/4885KMT2A 1153/4885

“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.