SCHEMBL259368

SCHEMBL259368

Cn1ccc(O)c(C#N)c1=O

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 4/20 0.59
CYP2C9 P11712 2/20 0.59
LMNA P02545 1/20 0.59
KDM4E B2RXH2 10/20 0.56
ALDH1A1 P00352 4/20 0.56
SMN1; SMN2 Q16637 2/20 0.56
BRD4 O60885 1/20 0.38
TAF1 P21675 1/20 0.38
BRPF1 P55201 1/20 0.38
CREBBP Q92793 1/20 0.38
CECR2 Q9BXF3 1/20 0.38
BRD9 Q9H8M2 1/20 0.38
KDM6A O15550 1/20 0.37
KDM4A O75164 1/20 0.37
CYP2C19 P33261 1/20 0.37
KDM5C P41229 1/20 0.37
KDM2B Q8NHM5 1/20 0.37
DOHH Q9BU89 1/20 0.37
KDM2A Q9Y2K7 1/20 0.37
MEN1 O00255 4/20 0.35

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
SCHEMBL4743181 0.78 LMNA (0.61) MAPTCYP2C9LMNAKDM4EALDH1A1
SCHEMBL25331540 0.77 LMNA (0.59) MAPTCYP2C9LMNAKDM4EALDH1A1
SCHEMBL16019365 0.77 PGR (0.37) MAPTCYP2C9LMNAKDM4EALDH1A1
SCHEMBL171187 0.75 GRM2 (0.54) LMNAKDM4EALDH1A1SMN1; SMN2MEN1
Ricinine SCHEMBL257955 0.74 MAPT (1.00) MAPTCYP2C9LMNAKDM4EALDH1A1
SCHEMBL26596828 0.74 LMNA (0.56) MAPTCYP2C9LMNAKDM4EALDH1A1
SCHEMBL4131086 0.74 GRM2 (0.42) KDM4EALDH1A1GRM2MAPK1
SCHEMBL169741 0.74 GRM2 (0.64) GRM2
SCHEMBL11212583 0.72 KDM4E (0.45) MAPTCYP2C9LMNAKDM4EALDH1A1
SCHEMBL16793353 0.72 ALDH1A1 (1.00) MAPTCYP2C9LMNAKDM4EALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12528816-B2 Substituted imidazo [1,2-b] pyridazines and [1, 2, 4] triazolo [ 4,3-b] pyridazines as camkii inhibitors CARDURION PHARMACEUTICALS, INC. (US) 2026-01-20 US disclosed
US-20240182474-A1 SUBSTITUTED IMIDAZO [1,2-b] PYRIDAZINES AND [1, 2, 4] TRIAZOLO [ 4,3-b] PYRIDAZINES AS CAMKII INHIBITORS CARDURION PHARMACEUTICALS, INC. 2024-06-06 US disclosed
WO-2024116528-A1 FLUORINE-CONTAINING PYRIDONE COMPOUND AND METHOD FOR PRODUCING SAME ユニマテック株式会社 2024-06-06 WO disclosed
CN-116940354-A Fused heteroaryl compounds and their use as CaMKII inhibitors 卡都瑞恩医药股份有限公司 2023-10-24 CN disclosed
US-11795172-B2 Substituted imidazo[1,2-b]pyridazines and [1,2,4]triazolo[4,3-b]pyridazines as CaMKII inhibitors CARDURION PHARMACEUTICALS, INC. (US) 2023-10-24 US disclosed
EP-4216948-A1 FUSED HETEROARYL COMPOUNDS AND THEIR USE AS CAMKII INHIBITORS Cardurion Pharmaceuticals, Inc. (US) 2023-08-02 EP disclosed
US-20220098207-A1 FUSED HETEROARYL COMPOUNDS AND THEIR USE AS CAMKII INHIBITORS CARDURION PHARMACEUTICALS, INC. 2022-03-31 US disclosed
WO-2022067082-A1 FUSED HETEROARYL COMPOUNDS AND THEIR USE AS CAMKII INHIBITORS CARDURION PHARMACEUTICALS, LLC (US) 2022-03-31 WO disclosed
US-9693556-B2 Herbicidal pyridazinone derivatives SYNGENTA LIMITED (GB) 2017-07-04 US disclosed
US-20140256546-A1 HERBICIDAL PYRIDAZINONE DERIVATIVES SYNGENTA LIMITED (GB) 2014-09-11 US disclosed
EP-2386861-A2 Cross-ß structure binding compounds Crossbeta Biosciences B.V. (NL) 2011-11-16 EP disclosed
CN-101835756-A 1, 4-disubstituted 3-cyano-pyridone derivatives and their use as positive MGLUR2 receptor modulators JANSSEN PHARMACEUTICA NV 2010-09-15 CN disclosed
CN-101679349-A 3-cyano-4- (4-phenyl-piperidin-1-yl) -pyridin-2-one derivatives JANSSEN PHARMACEUTICA NV 2010-03-24 CN disclosed
US-20100015126-A1 Methods of Binding of Cross-Beta Structures By Chaperones CROSSBETA BIOSCIENCES B.V. (NL) 2010-01-21 US disclosed
US-20100015126-A1 Methods of Binding of Cross-Beta Structures By Chaperones CROSSBETA BIOSCIENCES B.V. (NL) 2010-01-21 US disclosed
US-20090060866-A1 PHOSPHADIAZINE HCV POLYMERASE INHIBITORS I AND II IDENIX PHARMACEUTICALS, INC. (US) 2009-03-05 US disclosed
US-20080267948-A1 Croos-B Structure Binding Compounds CROSSBETA BIOSCIENCES B.V. (NL) 2008-10-30 US disclosed
US-20080267948-A1 Croos-B Structure Binding Compounds CROSSBETA BIOSCIENCES B.V. (NL) 2008-10-30 US disclosed
WO-2007108675-A1 METHODS OF BINDING OF CROSS-BETA STRUCTURES BY CHAPERONES CROSSBETA BIOSCIENCES B.V. (NL) 2007-09-27 WO disclosed
WO-2007008072-A2 CROSS-ß STRUCTURE BINDING COMPOUNDS CROSSBETA BIOSCIENCES B.V. (NL) 2007-01-18 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 (8 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-12528816-B2 Substituted imidazo [1,2-b] pyridazines and [1, 2, 4] triazolo [ 4,3-b] pyridazines as camkii inhibitors RYR2, CACNA1C, CAMK4 MAPT 4344/4885CYP2C9 1610/4885LMNA 1618/4885
US-20100015126-A1 Methods of Binding of Cross-Beta Structures By Chaperones HSP90B1, HSPB1, HSPA5 MAPT 1929/4885CYP2C9 4409/4885LMNA 2072/4885
US-20080267948-A1 Croos-B Structure Binding Compounds CACYBP, TBCB, MYCBP MAPT 2206/4885CYP2C9 4497/4885LMNA 1451/4885
US-20220098207-A1 FUSED HETEROARYL COMPOUNDS AND THEIR USE AS CAMKII INHIBITORS CAMK2B, CAMK2A, CAMK2G MAPT 2841/4885CYP2C9 1145/4885LMNA 3628/4885
US-20140256546-A1 HERBICIDAL PYRIDAZINONE DERIVATIVES PRDX6, PRDX1, CBR3 MAPT 4783/4885CYP2C9 88/4885LMNA 4229/4885
US-20240182474-A1 SUBSTITUTED IMIDAZO [1,2-b] PYRIDAZINES AND [1, 2, 4] TRIAZOLO [ 4,3-b] PYRIDAZINES AS CAMKII INHIBITORS CAMK2B, RYR2, CAMK2A MAPT 2976/4885CYP2C9 1491/4885LMNA 3703/4885
US-11795172-B2 Substituted imidazo[1,2-b]pyridazines and [1,2,4]triazolo[4,3-b]pyridazines as CaMKII inhibitors CAMK2B, RYR2, CAMK2A MAPT 2976/4885CYP2C9 1491/4885LMNA 3703/4885
US-20090060866-A1 PHOSPHADIAZINE HCV POLYMERASE INHIBITORS I AND II POLR2E, POLR2H, POLR2A MAPT 4141/4885CYP2C9 2562/4885LMNA 3922/4885

“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.