SCHEMBL4825839

SCHEMBL4825839

CNC1(C(=O)OC)CCCC1

nearest known ligand 0.49

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
MAPT P10636 1/20 0.49
NPSR1 Q6W5P4 1/20 0.48
ALDH1A1 P00352 1/20 0.46
L3MBTL1 Q9Y468 1/20 0.46
CYP4F2 P78329 1/20 0.40
CYP4A11 Q02928 1/20 0.40
KMT2A Q03164 2/20 0.38
KDM4E B2RXH2 1/20 0.38
CYP3A4 P08684 3/20 0.36
MEN1 O00255 1/20 0.36
LMNA P02545 1/20 0.34
CYP1A2 P05177 1/20 0.33
TSHR P16473 1/20 0.30

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
SCHEMBL5526779 0.98 MAPT (0.51) MAPTNPSR1ALDH1A1L3MBTL1CYP4F2
Hydrochloric Acid SCHEMBL17392798 0.98 MAPT (0.47) MAPTNPSR1ALDH1A1L3MBTL1CYP4F2
Hydrochloric Acid SCHEMBL5526775 0.96 MAPT (0.50) MAPTNPSR1ALDH1A1L3MBTL1CYP4F2
SCHEMBL16068213 0.95 MAPT (0.44) MAPTNPSR1ALDH1A1L3MBTL1CYP4F2
Hydrochloric Acid SCHEMBL17393194 0.93 MAPT (0.43) MAPTNPSR1ALDH1A1L3MBTL1CYP4F2
SCHEMBL1189812 0.90
Hydrochloric Acid SCHEMBL5523751 0.88 NPSR1 (0.40) MAPTNPSR1ALDH1A1L3MBTL1CYP4F2
SCHEMBL31252101 0.82 MAPT (0.46) MAPTNPSR1ALDH1A1L3MBTL1CYP4F2
SCHEMBL13981744 0.80 LMNA (0.39) MAPTNPSR1ALDH1A1L3MBTL1CYP4F2
SCHEMBL14865353 0.80 NPSR1 (0.35) MAPTNPSR1ALDH1A1L3MBTL1CYP4F2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250115585-A1 METHOD FOR PRODUCING DIHYDROPYRIDAZINE-3,5-DIONE DERIVATIVE CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-04-10 US disclosed
EP-4353718-A1 METHOD FOR PRODUCING DIHYDROPYRIDAZINE-3,5-DIONE DERIVATIVE CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-04-17 EP disclosed
CN-117460727-A Process for producing dihydropyridazine-3, 5-dione derivative 中外制药株式会社 2024-01-26 CN disclosed
WO-2022260062-A1 METHOD FOR PRODUCING DIHYDROPYRIDAZINE-3,5-DIONE DERIVATIVE 中外製薬株式会社 2022-12-15 WO disclosed
WO-2022260062-A1 METHOD FOR PRODUCING DIHYDROPYRIDAZINE-3,5-DIONE DERIVATIVE 中外製薬株式会社 2022-12-15 WO disclosed
EP-3192511-B1 PHARMACEUTICAL CONTAINING SODIUM-DEPENDENT PHOSPHATE TRANSPORTER INHIBITOR CHUGAI PHARMACEUTICAL CO LTD (JP) 2021-07-14 EP disclosed
EP-3757093-A1 DIHYDROPYRIDAZINE-3,5-DIONE DERIVATIVE CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2020-12-30 EP disclosed
EP-2975030-B1 DIHYDROPYRIDAZINE-3,5-DIONE DERIVATIVE CHUGAI PHARMACEUTICAL CO LTD (JP) 2020-07-15 EP disclosed
EP-3192511-A1 PHARMACEUTICAL CONTAINING SODIUM-DEPENDENT PHOSPHATE TRANSPORTER INHIBITOR Chugai Seiyaku Kabushiki Kaisha (JP) 2017-07-19 EP disclosed
US-9630989-B2 Dipeptide analogs for treating conditions associated with amyloid fibril formation RAMOT AT TEL-AVIV UNIVERSITY LTD. (IL) 2017-04-25 US disclosed
US-7348425-B2 Inhibitors of HCV replication BRISTOL-MYERS SQUIBB COMPANY (US) 2008-03-25 US disclosed
US-7348425-B2 Inhibitors of HCV replication BRISTOL-MYERS SQUIBB COMPANY (US) 2008-03-25 US disclosed
CN-101039947-A Inhibitors of hcv replication BRISTOL MYERS SQUIBB CO (US) 2007-09-19 CN disclosed
WO-2007092000-A1 INHIBITORS OF HCV REPLICATION BRISTOL-MYERS SQUIBB COMPANY (US) 2007-08-16 WO disclosed
WO-2007092000-A1 INHIBITORS OF HCV REPLICATION BRISTOL-MYERS SQUIBB COMPANY (US) 2007-08-16 WO disclosed
EP-1776368-A1 INHIBITORS OF HCV REPLICATION Bristol-Myers Squibb Company (US) 2007-04-25 EP disclosed
US-7153848-B2 Inhibitors of HCV replication BRISTOL-MYERS SQUIBB COMPANY (US) 2006-12-26 US disclosed
US-20060166964-A1 Inhibitors of HCV replication BRISTOL-MYERS SQUIBB COMPANY 2006-07-27 US disclosed
US-20060046983-A1 Inhibitors of HCV replication BRISTOL-MYERS SQUIBB COMPANY 2006-03-02 US disclosed
WO-2006020082-A1 INHIBITORS OF HCV REPLICATION BRISTOL-MYERS SQUIBB COMPANY (US) 2006-02-23 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-20250115585-A1 METHOD FOR PRODUCING DIHYDROPYRIDAZINE-3,5-DIONE DERIVATIVE QDPR, DHPS, DPYD MAPT 1823/4885NPSR1 3221/4885ALDH1A1 906/4885
US-20060166964-A1 Inhibitors of HCV replication EIF2AK2, HCCS, IDO1 MAPT 4274/4885NPSR1 3403/4885ALDH1A1 920/4885
US-20060046983-A1 Inhibitors of HCV replication EIF2AK2, HCCS, IDO1 MAPT 4274/4885NPSR1 3403/4885ALDH1A1 920/4885

“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.