SCHEMBL2798028

SCHEMBL2798028

O=C1CCC(c2ccccc2)=NN1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 1.00
AXL P30530 1/20 0.69
PDE3B Q13370 11/20 0.57
PDE3A Q14432 11/20 0.57
GPR119 Q8TDV5 1/20 0.57
KCNH2 Q12809 1/20 0.57
PDE2A O00408 2/20 0.55
LMNA P02545 2/20 0.54
MAPT P10636 2/20 0.54
NPY1R P25929 1/20 0.54
NPY2R P49146 1/20 0.54
PDE4A P27815 3/20 0.53
PDE4B Q07343 3/20 0.53
PDE4C Q08493 3/20 0.53
PDE4D Q08499 3/20 0.53
CYP1A2 P05177 1/20 0.53
CYP3A4 P08684 1/20 0.53
CYP2D6 P10635 1/20 0.53
CYP2C9 P11712 1/20 0.53
TSHR P16473 1/20 0.53

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
SCHEMBL10353452 0.90 SMN1; SMN2 (0.81) SMN1; SMN2AXLPDE3BPDE3AKCNH2
SCHEMBL8800856 0.86 SMN1; SMN2 (0.73) SMN1; SMN2AXLPDE3BPDE3AGPR119
SCHEMBL11158097 0.85 SMN1; SMN2 (0.73) SMN1; SMN2AXLPDE3BPDE3AGPR119
SCHEMBL7263634 0.82 KCNH2 (0.73) SMN1; SMN2AXLPDE3BPDE3AKCNH2
SCHEMBL927560 0.82 SMN1; SMN2 (0.70) SMN1; SMN2PDE3BPDE3AKCNH2PDE2A
SCHEMBL9687996 0.82 SMN1; SMN2 (0.70) SMN1; SMN2PDE3BPDE3AKCNH2PDE2A
SCHEMBL2375581 0.82 AXL (1.00) SMN1; SMN2AXLPDE3BPDE3AGPR119
SCHEMBL6331085 0.81 SMN1; SMN2 (0.68) SMN1; SMN2PDE3BPDE3AKCNH2PDE2A
SCHEMBL2846257 0.81 SMN1; SMN2 (0.68) SMN1; SMN2PDE3BPDE3AKCNH2PDE2A
SCHEMBL8302890 0.81 SMN1; SMN2 (0.68) SMN1; SMN2PDE3BPDE3AKCNH2PDE2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8747643-B2 Plating bath and method ROHM AND HAAS ELECTRONIC MATERIALS LLC (US) 2014-06-10 US claimed
US-20140027298-A1 PLATING BATH AND METHOD ROHM & HAAS ELECT MAT (US) 2014-01-30 US claimed
US-20130048505-A1 PLATING BATH AND METHOD ROHM AND HAAS ELECTRONIC MATERIALS LLC (US) 2013-02-28 US claimed
EP-0327800-B1 6-PHENYLDIHYDRO-3(2H)-PYRIDAZINONES, PROCESS FOR THEIR PREPARATION AND MEDICINES CONTAINING THESE COMPOUNDS HEUMANN PHARMA GMBH & CO (DE) 1992-05-27 EP claimed
US-4954501-A INOTROPIC AGENTS HEUMANN PHARMA GMBH & CO. (DE) 1990-09-04 US claimed
EP-0327800-A2 6-Phenyldihydro-3(2H)-pyridazinones, process for their preparation and medicines containing these compounds HEUMANN PHARMA GMBH & CO (DE) 1989-08-16 EP claimed
US-4397854-A INCREASE IN MYOCARDIAL CONTRACTILITY WARNER-LAMBERT COMPANY (US) 1983-08-09 US claimed
US-4255571-A Catalytic dehydrogenation preparation of 3-pyridazones HOECHST AKTIENGESELLSCHAFT (DE) 1981-03-10 US claimed
US-20250115573-A1 PYRIDAZINE-BASED PYRIDINE DERIVATIVES AS BIOLOGICALLY ACTIVE AGENTS IMRAN MOHD (SA) 2025-04-10 US disclosed
CN-115894324-B Method for preparing pyrrolidone compound 华北电力大学 2024-08-27 CN disclosed
US-20240182452-A1 6-PHENYL-4,5-DIHYDROPYRIDAZIN-3(2H)-ONE DERIVATIVES AS PDE3A AND PDE3B INHIBITORS FOR TREATING CANCER BAYER AKTIENGESELLSCHAFT (DE) 2024-06-06 US disclosed
US-11897867-B2 6-phenyl-4,5-dihydropyridazin-3(2H)-one derivatives as PDE3A and PDE3B inhibitors for treating cancer BAYER AKTIENGESELLSCHAFT (DE) 2024-02-13 US disclosed
US-11897867-B2 6-phenyl-4,5-dihydropyridazin-3(2H)-one derivatives as PDE3A and PDE3B inhibitors for treating cancer BAYER AKTIENGESELLSCHAFT (DE) 2024-02-13 US disclosed
US-11730726-B2 Dimeric immuno-modulatory compounds against cereblon-based mechanisms H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. (US) 2023-08-22 US disclosed
EP-0042513-A1 Dihydropyridazinones, processes for their preparation and pharmaceutical compositions containing these compounds BASF Aktiengesellschaft (DE) 1981-12-30 EP disclosed
US-4298609-A 4,5-Dihydro-6-(4-pyridinyl)-3-pyridazinol and salts, their preparation and use as blood pressure lowering agents STERLING DRUG INC. (US) 1981-11-03 US disclosed
US-4293554-A Method of treating asthma AMERICAN CYANAMID COMPANY (US) 1981-10-06 US disclosed
EP-0002719-B1 PROCESS FOR THE PREPARATION OF 3-PYRIDAZINONES HOECHST AKTIENGESELLSCHAFT (DE) 1981-06-24 EP disclosed
US-4255571-A Catalytic dehydrogenation preparation of 3-pyridazones HOECHST AKTIENGESELLSCHAFT (DE) 1981-03-10 US disclosed
EP-0002719-A2 Process for the preparation of 3-pyridazinones HOECHST AKTIENGESELLSCHAFT (DE) 1979-07-11 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 (5 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-11730726-B2 Dimeric immuno-modulatory compounds against cereblon-based mechanisms CRBN, CD4, CD74 SMN1; SMN2 1672/4885AXL 4760/4885PDE3B 3879/4885
US-20240182452-A1 6-PHENYL-4,5-DIHYDROPYRIDAZIN-3(2H)-ONE DERIVATIVES AS PDE3A AND PDE3B INHIBITORS FOR TREATING CANCER PDE3A, PDE3B, PDE5A SMN1; SMN2 3303/4885AXL 4571/4885PDE3B 2/4885
US-20130048505-A1 PLATING BATH AND METHOD EPHX1, CYP7B1, AOC3 SMN1; SMN2 1955/4885AXL 4463/4885PDE3B 843/4885
US-20250115573-A1 PYRIDAZINE-BASED PYRIDINE DERIVATIVES AS BIOLOGICALLY ACTIVE AGENTS HRH4, HRH3, CBR3 SMN1; SMN2 2953/4885AXL 2899/4885PDE3B 456/4885
US-11897867-B2 6-phenyl-4,5-dihydropyridazin-3(2H)-one derivatives as PDE3A and PDE3B inhibitors for treating cancer PDE3B, PDE3A, PDE5A SMN1; SMN2 3985/4885AXL 4594/4885PDE3B 1/4885

“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.