SCHEMBL145975

SCHEMBL145975

CS(=O)(=O)NCCNC(=O)O

nearest known ligand 0.39

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
KDM4D Q6B0I6 1/20 0.39
POLB P06746 2/20 0.38
PTGES O14684 1/20 0.38
KMT2A Q03164 1/20 0.37
USP2 O75604 1/20 0.37
ALDH1A1 P00352 2/20 0.36
MAPT P10636 1/20 0.36
CYP2D6 P10635 1/20 0.36
CYP2C19 P33261 1/20 0.36
RECQL P46063 2/20 0.35
KDM4E B2RXH2 1/20 0.35
TSHR P16473 1/20 0.35
MALT1 Q9UDY8 1/20 0.34
CA2 P00918 1/20 0.33
SCN9A Q15858 1/20 0.33
EGLN1 Q9GZT9 2/20 0.32
NPC1 O15118 1/20 0.32
RAB9A P51151 1/20 0.32
SMN1; SMN2 Q16637 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
SCHEMBL146344 0.86 ALDH1A1 (0.46) KDM4DPOLBPTGESKMT2AALDH1A1
SCHEMBL3863697 0.86 POLB (0.44) POLBPTGESKMT2AALDH1A1KDM4E
SCHEMBL4773600 0.85 EPHX2 (0.43) POLBKMT2AALDH1A1KDM4ECA2
SCHEMBL1912202 0.81 MAPK1 (0.48) KDM4DPOLBPTGESALDH1A1KDM4E
SCHEMBL23011666 0.79 KDM4D (0.35) KDM4DPOLBPTGESKMT2AALDH1A1
SCHEMBL21798197 0.79 PTGES (0.39) POLBPTGESKMT2AUSP2ALDH1A1
SCHEMBL5841992 0.79 KDM4D (0.35) KDM4DPOLBPTGESKMT2AALDH1A1
SCHEMBL21766639 0.79 MEN1 (0.56) KDM4DKMT2AALDH1A1CYP2C19RECQL
SCHEMBL5841987 0.79 KDM4D (0.35) KDM4DPOLBPTGESKMT2AALDH1A1
SCHEMBL3043384 0.79 POLB (0.44) KDM4DPOLBALDH1A1MAPTRECQL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3609888-A1 FARNESOID X RECEPTOR AGONISTS AND USES THEREOF Metacrine, Inc. (US) 2020-02-19 EP claimed
WO-2018170182-A1 FARNESOID X RECEPTOR AGONISTS AND USES THEREOF METACRINE, INC. (US) 2018-09-20 WO claimed
US-20240173303-A1 1,2,5-Oxadiazoles As Inhibitors Of Indoleamine 2,3- Dioxygenase INCYTE HOLDINGS CORPORATION 2024-05-30 US disclosed
EP-2911669-B1 SYNERGISTIC COMBINATION OF IMMUNOLOGIC INHIBITORS FOR THE TREATMENT OF CANCER UNIV CHICAGO (US) 2024-04-10 EP disclosed
US-11242323-B2 Inhibition of OLIG2 activity Curtana Pharmaceuticals, Inc. (US) 2022-02-08 US disclosed
US-11236071-B1 Farnesoid X receptor agonists and uses thereof METACRINE, INC. (US) 2022-02-01 US disclosed
US-11207302-B2 1,2,5-oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase INCYTE CORPORATION (US) 2021-12-28 US disclosed
US-20210253535-A1 INHIBITION OF OLIG2 ACTIVITY Curtana Pharmaceuticals, Inc. 2021-08-19 US disclosed
US-20210228715-A1 SYNERGISTIC COMBINATION OF IMMUNOLOGIC INHIBITORS FOR THE TREATMENT OF CANCER THE UNIVERSITY OF CHICAGO (US) 2021-07-29 US disclosed
US-10967060-B2 Synergistic combination of immunologic inhibitors for the treatment of cancer THE UNIVERSITY OF CHICAGO (US) 2021-04-06 US disclosed
US-20210030722-A1 1,2,5-Oxadiazoles As Inhibitors Of Indoleamine 2,3- Dioxygenase INCYTE CORPORATION 2021-02-04 US disclosed
WO-2014066834-A1 SYNERGISTIC COMBINATION OF IMMUNOLOGIC INHIBITORS FOR THE TREATMENT OF CANCER THE UNIVERSITY OF CHICAGO (US) 2014-05-01 WO disclosed
US-20140023663-A1 1,2,5-Oxadiazoles As Inhibitors Of Indoleamine 2,3-Dioxygenase INCYTE CORPORATION (US) 2014-01-23 US disclosed
US-20120058079-A1 1,2,5-Oxadiazoles as Inhibitors of Indoleamine 2,3-Dioxygenase INCYTE CORPORATION, A DELAWARE CORPORATION 2012-03-08 US disclosed
US-8088803-B2 1,2,5-oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase INCYTE CORPORATION (US) 2012-01-03 US disclosed
EP-2315756-A2 1,2,5-OXADIAZOLES AS INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE Incyte Corporation (US) 2011-05-04 EP disclosed
US-20110015225-A1 Heterocyclic compound TAKEDA PHARMACEUTICAL COMPANY LIMITED 2011-01-20 US disclosed
EP-2261213-A1 HETEROCYCLIC COMPOUND Takeda Pharmaceutical Company Limited (JP) 2010-12-15 EP disclosed
US-20100015178-A1 1,2,5-OXADIAZOLES AS INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE INCYTE CORPORATION 2010-01-21 US disclosed
WO-2010005958-A2 1,2,5-OXADIAZOLES AS INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE INCYTE CORPORATION (US) 2010-01-14 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 (12 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-20210030722-A1 1,2,5-Oxadiazoles As Inhibitors Of Indoleamine 2,3- Dioxygenase IDO1, IDO2, INMT KDM4D 578/4885POLB 2730/4885PTGES 1397/4885
US-20240173303-A1 1,2,5-Oxadiazoles As Inhibitors Of Indoleamine 2,3- Dioxygenase IDO1, IDO2, INMT KDM4D 578/4885POLB 2730/4885PTGES 1397/4885
US-20210253535-A1 INHIBITION OF OLIG2 ACTIVITY GLI2, ING2, GMFG KDM4D 3373/4885POLB 1413/4885PTGES 2558/4885
US-11207302-B2 1,2,5-oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase IDO1, IDO2, INMT KDM4D 578/4885POLB 2730/4885PTGES 1397/4885
US-20140023663-A1 1,2,5-Oxadiazoles As Inhibitors Of Indoleamine 2,3-Dioxygenase IDO1, IDO2, INMT KDM4D 578/4885POLB 2730/4885PTGES 1397/4885
US-20100015178-A1 1,2,5-OXADIAZOLES AS INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE IDO1, IDO2, INMT KDM4D 578/4885POLB 2730/4885PTGES 1397/4885
US-20210228715-A1 SYNERGISTIC COMBINATION OF IMMUNOLOGIC INHIBITORS FOR THE TREATMENT OF CANCER ICOS, CD274, IDO1 KDM4D 122/4885POLB 4503/4885PTGES 2638/4885
US-11236071-B1 Farnesoid X receptor agonists and uses thereof NR1H4, NR1H2, NR1H3 KDM4D 4852/4885POLB 4062/4885PTGES 413/4885
US-20120058079-A1 1,2,5-Oxadiazoles as Inhibitors of Indoleamine 2,3-Dioxygenase IDO1, IDO2, INMT KDM4D 578/4885POLB 2730/4885PTGES 1397/4885
US-11242323-B2 Inhibition of OLIG2 activity POU2F2, ING2, PAX2 KDM4D 2910/4885POLB 935/4885PTGES 2516/4885
US-10967060-B2 Synergistic combination of immunologic inhibitors for the treatment of cancer ICOS, IDO1, IL2 KDM4D 143/4885POLB 3342/4885PTGES 2779/4885
US-20110015225-A1 Heterocyclic compound MC1R, MCHR1, MCHR2 KDM4D 3798/4885POLB 4615/4885PTGES 3931/4885

“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.