SCHEMBL1785556

SCHEMBL1785556

CCCc1c(C=O)c(C)c(C(=O)OCC)n1O

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 0.42
LMNA P02545 4/20 0.41
KDM4E B2RXH2 1/20 0.41
KMT2A Q03164 3/20 0.39
CYP3A4 P08684 2/20 0.38
USP2 O75604 2/20 0.38
ALDH1A1 P00352 4/20 0.36
MEN1 O00255 1/20 0.36
POLB P06746 1/20 0.36
MAPT P10636 4/20 0.36
NPSR1 Q6W5P4 2/20 0.36
HTT P42858 1/20 0.35
TSHR P16473 4/20 0.35
HPGD P15428 3/20 0.35
CYP1A2 P05177 1/20 0.35
CYP2D6 P10635 1/20 0.35
CYP2C19 P33261 1/20 0.35
L3MBTL1 Q9Y468 1/20 0.35
GAA P10253 2/20 0.34
MAPK1 P28482 1/20 0.33

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
SCHEMBL1782394 0.90 SMN1; SMN2 (0.39) SMN1; SMN2LMNAKDM4EKMT2ACYP3A4
SCHEMBL12650842 0.90 SMN1; SMN2 (0.43) SMN1; SMN2LMNAKDM4EKMT2ACYP3A4
SCHEMBL1787366 0.88 SMN1; SMN2 (0.44) SMN1; SMN2LMNAKDM4EKMT2ACYP3A4
SCHEMBL20504192 0.86 SMN1; SMN2 (0.40) SMN1; SMN2LMNAKDM4EKMT2ACYP3A4
SCHEMBL18891004 0.84 SMN1; SMN2 (0.41) SMN1; SMN2LMNAKDM4EKMT2ACYP3A4
SCHEMBL1785884 0.83
SCHEMBL1787283 0.83 MAPT (0.45) SMN1; SMN2LMNAKDM4EKMT2AALDH1A1
SCHEMBL1785133 0.81 KMT2A (0.46) SMN1; SMN2LMNAKDM4EKMT2ACYP3A4
SCHEMBL1783972 0.73
SCHEMBL18891239 0.73 SMN1; SMN2 (0.39) SMN1; SMN2LMNAKDM4EKMT2ACYP3A4

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
US-20250320216-A1 PHOSPHODIESTERASE INHIBITORS AND USES THEREOF TOPADUR PHARMA AG (CH) 2025-10-16 US disclosed
US-12351585-B2 2-phenyl-3,4-dihydropyrrolo[2,1-f] [1,2,4]triazinone derivatives as phosphodiesterase inhibitors and uses thereof TOPADUR PHARMA AG (CH) 2025-07-08 US disclosed
US-20240343730-A1 2-PHENYL-3,4-DIHYDROPYRROLO[2,1 -F] [1,2,4]TRIAZINONE DERIVATIVES AS PHOSPHODIESTERASE INHIBITORS AND USES THEREOF TOPADUR PHARMA AG (CH) 2024-10-17 US disclosed
US-11897890-B2 2-phenyl-3,4-dihydropyrrolo[2,1 -f] [1,2,4]triazinone derivatives as phosphodiesterase inhibitors and uses thereof TOPADUR PHARMA AG (CH) 2024-02-13 US disclosed
US-20220169655-A1 2-PHENYL-3,4-DIHYDROPYRROLO[2,1 -F] [1,2,4]TRIAZINONE DERIVATIVES AS PHOSPHODIESTERASE INHIBITORS AND USES THEREOF TOPADUR PHARMA AG (CH) 2022-06-02 US disclosed
US-20220169655-A1 2-PHENYL-3,4-DIHYDROPYRROLO[2,1 -F] [1,2,4]TRIAZINONE DERIVATIVES AS PHOSPHODIESTERASE INHIBITORS AND USES THEREOF TOPADUR PHARMA AG (CH) 2022-06-02 US disclosed
EP-3377495-B1 2-PHENYL-3,4-DIHYDROPYRROLO[2,1-F] [1,2,4]TRIAZINONE DERIVATIVES AS PHOSPHODIESTERASE INHIBITORS AND USES THEREOF TOPADUR PHARMA AG (CH) 2022-03-16 EP disclosed
US-11242347-B2 2-phenyl-3,4-dihydropyrrolo[2,1-Ff] [1,2,4]triazinone derivatives as phosphodiesterase inhibitors and uses thereof TOPADUR PHARMA AG (CH) 2022-02-08 US disclosed
US-11242347-B2 2-phenyl-3,4-dihydropyrrolo[2,1-Ff] [1,2,4]triazinone derivatives as phosphodiesterase inhibitors and uses thereof TOPADUR PHARMA AG (CH) 2022-02-08 US disclosed
CN-108290896-B 2-phenyl-3, 4-dihydropyrrolo [2,1-F ] [1,2,4] triazinone derivatives and uses thereof 托帕杜制药公司 2021-09-28 CN disclosed
US-20200239478-A1 2-PHENYL-3,4-DIHYDROPYRROLO[2,1 -F] [1,2,4]TRIAZINONE DERIVATIVES AS PHOSPHODIESTERASE INHIBITORS AND USES THEREOF TOPADUR PHARMA AG (CH) 2020-07-30 US disclosed
US-10570137-B2 2-phenyl-3,4-dihydropyrrolo[2,1 -F] [1,2,4]triazinone derivatives as phosphodiesterase inhibitors and uses thereof TOPADUR PHARMA AG (CH) 2020-02-25 US disclosed
US-10570137-B2 2-phenyl-3,4-dihydropyrrolo[2,1 -F] [1,2,4]triazinone derivatives as phosphodiesterase inhibitors and uses thereof TOPADUR PHARMA AG (CH) 2020-02-25 US disclosed
US-20180312513-A1 2-PHENYL-3,4-DIHYDROPYRROLO[2,1 -F] [1,2,4]TRIAZINONE DERIVATIVES AS PHOSPHODIESTERASE INHIBITORS AND USES THEREOF TOPADUR PHARMA AG (CH) 2018-11-01 US disclosed
EP-3377495-A1 2-PHENYL-3,4-DIHYDROPYRROLO[2,1 -F][1,2,4]TRIAZINONE DERIVATIVES AS PHOSPHODIESTERASE INHIBITORS AND USES THEREOF Topadur Pharma AG (CH) 2018-09-26 EP disclosed
WO-2017085056-A1 2-PHENYL-3,4-DIHYDROPYRROLO[2,1 -F] [1,2,4]TRIAZINONE DERIVATIVES AS PHOSPHODIESTERASE INHIBITORS AND USES THEREOF TOPADUR PHARMA AG (CH) 2017-05-26 WO disclosed
US-8273901-B2 Process of forming a pyrrole compound Nanyang Technical University (SG) 2012-09-25 US disclosed
US-8273901-B2 Process of forming a pyrrole compound Nanyang Technical University (SG) 2012-09-25 US disclosed
US-20110124881-A1 PROCESS OF FORMING A PYRROLE COMPOUND NANYANG TECHNOLOGICAL UNIVERSITY (SG) 2011-05-26 US disclosed
US-20110124881-A1 PROCESS OF FORMING A PYRROLE COMPOUND NANYANG TECHNOLOGICAL UNIVERSITY (SG) 2011-05-26 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 (10 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-20110124881-A1 PROCESS OF FORMING A PYRROLE COMPOUND OXER1, OGDH, OPRD1 SMN1; SMN2 1650/4885LMNA 3028/4885KDM4E 1362/4885
US-20220169655-A1 2-PHENYL-3,4-DIHYDROPYRROLO[2,1 -F] [1,2,4]TRIAZINONE DERIVATIVES AS PHOSPHODIESTERASE INHIBITORS AND USES THEREOF PDE7A, GNAO1, PDE3A SMN1; SMN2 3993/4885LMNA 2511/4885KDM4E 3617/4885
US-11242347-B2 2-phenyl-3,4-dihydropyrrolo[2,1-Ff] [1,2,4]triazinone derivatives as phosphodiesterase inhibitors and uses thereof PDE7A, PDE3A, CHRM3 SMN1; SMN2 3944/4885LMNA 2605/4885KDM4E 3830/4885
US-20240343730-A1 2-PHENYL-3,4-DIHYDROPYRROLO[2,1 -F] [1,2,4]TRIAZINONE DERIVATIVES AS PHOSPHODIESTERASE INHIBITORS AND USES THEREOF PDE7A, PDE3A, GNAO1 SMN1; SMN2 3963/4885LMNA 2493/4885KDM4E 3702/4885
US-20250320216-A1 PHOSPHODIESTERASE INHIBITORS AND USES THEREOF PDE7A, PDE3A, PDE3B SMN1; SMN2 3935/4885LMNA 2421/4885KDM4E 3760/4885
US-20180312513-A1 2-PHENYL-3,4-DIHYDROPYRROLO[2,1 -F] [1,2,4]TRIAZINONE DERIVATIVES AS PHOSPHODIESTERASE INHIBITORS AND USES THEREOF PDE7A, GNAO1, PDE3A SMN1; SMN2 3993/4885LMNA 2511/4885KDM4E 3617/4885
US-10570137-B2 2-phenyl-3,4-dihydropyrrolo[2,1 -F] [1,2,4]triazinone derivatives as phosphodiesterase inhibitors and uses thereof PDE7A, GNAO1, PDE3A SMN1; SMN2 3993/4885LMNA 2511/4885KDM4E 3617/4885
US-20200239478-A1 2-PHENYL-3,4-DIHYDROPYRROLO[2,1 -F] [1,2,4]TRIAZINONE DERIVATIVES AS PHOSPHODIESTERASE INHIBITORS AND USES THEREOF PDE7A, GNAO1, PDE3A SMN1; SMN2 3993/4885LMNA 2511/4885KDM4E 3617/4885
US-11897890-B2 2-phenyl-3,4-dihydropyrrolo[2,1 -f] [1,2,4]triazinone derivatives as phosphodiesterase inhibitors and uses thereof PDE7A, GNAO1, PDE3A SMN1; SMN2 3993/4885LMNA 2511/4885KDM4E 3617/4885
US-12351585-B2 2-phenyl-3,4-dihydropyrrolo[2,1-f] [1,2,4]triazinone derivatives as phosphodiesterase inhibitors and uses thereof PDE7A, PDE3A, GNAO1 SMN1; SMN2 3963/4885LMNA 2493/4885KDM4E 3702/4885

“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.