SCHEMBL934680

SCHEMBL934680

Cc1cc(=O)[nH]nc1-c1ccc(N)cc1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDE3B Q13370 3/20 0.56
PDE3A Q14432 3/20 0.56
HRH3 Q9Y5N1 2/20 0.50
PDGFRB P09619 4/20 0.49
CDK8 P49336 3/20 0.49
NTRK3 Q16288 3/20 0.49
NTRK2 Q16620 3/20 0.49
AURKB Q96GD4 2/20 0.49
MET P08581 1/20 0.49
ROCK1 Q13464 1/20 0.49
CLK4 Q9HAZ1 1/20 0.49
GPR119 Q8TDV5 3/20 0.45
NTRK1 P04629 2/20 0.44
RET P07949 2/20 0.44
MAPK14 Q16539 2/20 0.44
HPGD P15428 2/20 0.44
LTK P29376 1/20 0.44
FLT3 P36888 1/20 0.44
LMNA P02545 2/20 0.43
TSHR P16473 1/20 0.43

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
SCHEMBL10353678 0.91 PDE3B (0.63) PDE3BPDE3AHRH3PDGFRBCDK8
SCHEMBL11116797 0.90 LMNA (0.56) PDE3BPDE3AHRH3PDGFRBCDK8
Cadaverine Tartrate SCHEMBL8944439 0.87 PDGFRB (0.49) PDE3BPDE3AHRH3PDGFRBCDK8
SCHEMBL11632009 0.83 PDE3B (0.56) PDE3BPDE3AHRH3PDGFRBCDK8
SCHEMBL11396639 0.83 HPGD (0.60) PDE3BPDE3AHRH3PDGFRBCDK8
SCHEMBL11474002 0.83 PDE3B (0.56) PDE3BPDE3AHRH3PDGFRBCDK8
SCHEMBL2844945 0.83 PDE3B (0.56) PDE3BPDE3AHRH3PDGFRBCDK8
SCHEMBL8481283 0.83 PDGFRB (0.59) PDE3BPDE3AHRH3PDGFRBCDK8
SCHEMBL8898020 0.82 HPGD (0.64) PDE3BPDE3AHRH3PDGFRBCDK8
SCHEMBL5678928 0.82 PDE3B (0.56) PDE3BPDE3AHRH3PDGFRBCDK8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20120165524-A1 Process for Preparing Levosimendan and Intermediates for Use in the Process CIPLA LIMITED (IN) 2012-06-28 US claimed
EP-2454241-A1 PROCESS FOR PREPARING LEVOSIMENDAN AND INTERMEDIATES FOR USE IN THE PROCESS CIPLA LIMITED (IN) 2012-05-23 EP claimed
WO-2011007123-A1 PROCESS FOR PREPARING LEVOSIMENDAN AND INTERMEDIATES FOR USE IN THE PROCESS CIPLA LIMITED (IN) 2011-01-20 WO claimed
EP-0791584-A1 OPTICALLY ACTIVE COMPOUND NIPPON SODA CO., LTD. (JP) 1997-08-27 EP claimed
US-5424428-A Optical resolution of a drug chemical intermediates 6-(4-amino phenyl)-5-methylpyridazin-3(2H)one by salt-formation with tartaric acid in 2-propanol, desalting by basification ORION-YHTYMA OY (FI) 1995-06-13 US claimed
EP-0565546-B1 (-)-[[4-(1,4,5,6-TETRAHYDRO-4-METHYL-6-OXO-3-PYRIDAZINYL)PHENYL]-HYDRAZONO]PROPANEDINITRILE ORION YHTYMAE OY (FI) 1995-03-08 EP claimed
WO-1992012135-A1 (-)-[[4-(1,4,5,6-TETRAHYDRO-4-METHYL-6-OXO-3-PYRIDAZINYL)PHENYL]-HYDRAZONO]PROPANEDINITRILE Orion-Yhtymä Oy (FI) 1992-07-23 WO claimed
JP-9183767-A None JP disclosed
US-12590071-B2 Hydrazone derivative in which terminal amine group is substituted with aryl group or heteroaryl group, and use thereof KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2026-03-31 US disclosed
CN-113727972-B Novel hydrazone derivatives having terminal amine groups substituted with aryl or heteroaryl groups and use thereof 韩国科学技术研究院 2024-12-27 CN disclosed
EP-4274576-A1 PROCESS FOR THE PREPARATION OF HIGH PURITY LEVOSIMENDAN Navinta, LLC (US) 2023-11-15 EP disclosed
US-11760730-B2 Process for the preparation of high purity Levosimendan NAVINTA, LLC (US) 2023-09-19 US disclosed
US-20220396553-A1 NOVEL HYDRAZONE DERIVATIVE IN WHICH TERMINAL AMINE GROUP IS SUBSTITUTED WITH ARYL GROUP OR HETEROARYL GROUP, AND USE THEREOF KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2022-12-15 US disclosed
EP-0565546-B1 (-)-[[4-(1,4,5,6-TETRAHYDRO-4-METHYL-6-OXO-3-PYRIDAZINYL)PHENYL]-HYDRAZONO]PROPANEDINITRILE ORION YHTYMAE OY (FI) 1995-03-08 EP disclosed
US-5185332-A Treating congestive heart failure ORION-YHTYMA OY (FI) 1993-02-09 US disclosed
WO-1992012135-A1 (-)-[[4-(1,4,5,6-TETRAHYDRO-4-METHYL-6-OXO-3-PYRIDAZINYL)PHENYL]-HYDRAZONO]PROPANEDINITRILE Orion-Yhtymä Oy (FI) 1992-07-23 WO disclosed
US-5122524-A Treatment for congestive heart failure; hypertensive agents; vasodilation ORION-YHTYMA OY (FI) 1992-06-16 US disclosed
US-5019575-A Congestive Heart Failure Treatment ORION-YHTYMA OY (FI) 1991-05-28 US disclosed
EP-0383449-A2 Pyridazinone derivatives and processes for preparing the same ORION-YHTYMÀ„ OY (FI) 1990-08-22 EP disclosed
EP-0116853-A1 Pyridazinones, processes for preparing them, therapeutical compositions containing these compounds and their use BASF Aktiengesellschaft (DE) 1984-08-29 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 (4 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-20120165524-A1 Process for Preparing Levosimendan and Intermediates for Use in the Process CYP3A5, HTR5A, CYP2D6 PDE3B 375/4885PDE3A 220/4885HRH3 2202/4885
US-11760730-B2 Process for the preparation of high purity Levosimendan SRD5A2, SRD5A1, TNNC1 PDE3B 181/4885PDE3A 144/4885HRH3 3651/4885
US-12590071-B2 Hydrazone derivative in which terminal amine group is substituted with aryl group or heteroaryl group, and use thereof ABL1, TH, CYP3A43 PDE3B 491/4885PDE3A 437/4885HRH3 299/4885
US-20220396553-A1 NOVEL HYDRAZONE DERIVATIVE IN WHICH TERMINAL AMINE GROUP IS SUBSTITUTED WITH ARYL GROUP OR HETEROARYL GROUP, AND USE THEREOF AANAT, NAT1, HNMT PDE3B 2067/4885PDE3A 2125/4885HRH3 27/4885

“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.