SCHEMBL2600259

SCHEMBL2600259

CN1CCCC(C(=O)NN)C1

nearest known ligand 0.44

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
BCHE P06276 3/20 0.41
TSHR P16473 1/20 0.41
ALDH1A1 P00352 3/20 0.40
PKM P14618 1/20 0.40
ITGB3 P05106 1/20 0.40
ITGA2B P08514 1/20 0.40
F2R P25116 1/20 0.40
PARP1 P09874 4/20 0.39
LMNA P02545 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.38
MAPK1 P28482 1/20 0.36
KDM4E B2RXH2 1/20 0.36
HTT P42858 1/20 0.36

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
SCHEMBL6582811 1.00 BCHE (0.41) BCHETSHRALDH1A1PKMITGB3
SCHEMBL19550801 1.00 BCHE (0.41) BCHETSHRALDH1A1PKMITGB3
SCHEMBL26971791 0.83 BCHE (0.56) BCHETSHRALDH1A1PKMITGB3
SCHEMBL2600287 0.83 BCHE (0.56) BCHETSHRALDH1A1PKMITGB3
SCHEMBL13045996 0.80 BCHE (0.43) BCHETSHRALDH1A1PKMITGB3
SCHEMBL6991659 0.80 ALDH1A1 (0.42) BCHETSHRALDH1A1PKMITGB3
SCHEMBL3315913 0.80 TSHR (0.62) BCHETSHRITGB3ITGA2BF2R
SCHEMBL2600258 0.79 BCHE (0.39) BCHETSHRALDH1A1PKMITGB3
SCHEMBL20837312 0.79 MAPK8 (0.44) ALDH1A1ITGB3ITGA2BLMNAMAPK1
SCHEMBL13999836 0.79 BCHE (0.62) BCHETSHRALDH1A1ITGB3ITGA2B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12060357-B2 9-substituted amino triazolo quinazoline derivatives as adenosine receptor antagonists, pharmaceutical compositions and their use MERCK SHARP & DOHME LLC (US) 2024-08-13 US disclosed
US-20220220117-A1 9-SUBSTITUTED AMINO TRIAZOLO QUINAZOLINE DERIVATIVES AS ADENOSINE RECEPTOR ANTAGONISTS, PHARMACEUTICAL COMPOSITIONS AND THEIR USE MERCK SHARP & DOHME CORP. (US) 2022-07-14 US disclosed
EP-3452466-B1 HETEROCYCLIC TRIAZOLE COMPOUNDS AS AGONISTS OF THE APJ RECEPTOR AMGEN INC (US) 2020-08-12 EP disclosed
WO-2019055750-A1 PYRAZOLOPYRIMIDINONE COMPOUNDS AND USES THEREOF Aduro Biotech, Inc. (US) 2019-03-21 WO disclosed
US-10150760-B2 Compounds for use in preparing heterocyclic triazole agonists of the APJ receptor AMGEN INC. (US) 2018-12-11 US disclosed
US-20180222895-A1 COMPOUNDS FOR USE IN PREPARING HETEROCYCLIC TRIAZOLE AGONISTS OF THE APJ RECEPTOR AMGEN INC. 2018-08-09 US disclosed
US-9988369-B2 Heterocyclic triazole compounds as agonists of the APJ receptor AMGEN INC. (US) 2018-06-05 US disclosed
US-20170320860-A1 HETEROCYCLIC TRIAZOLE COMPOUNDS AS AGONISTS OF THE APJ RECEPTOR AMGEN INC. 2017-11-09 US disclosed
US-8163775-B2 Allosteric modulators of metabotropic glutamate receptors ADDEX PHARMA SA (CH) 2012-04-24 US disclosed
US-20120022108-A1 ALLOSTERIC MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS ADDEX PHARMA SA (CH) 2012-01-26 US disclosed
WO-2009017874-A9 NOVEL CURCUMIN DERIVATIVES AND THEIR PHARMACEUTICAL USES THEREOF UNIV ROCHESTER (US) 2009-03-19 WO disclosed
WO-2009023357-A2 CURCUMIN DERIVATIVES AND THEIR USE AS RADIOPROTECTORS UNIVERSITY OF ROCHESTER (US) 2009-02-19 WO disclosed
WO-2009017874-A2 NOVEL CURCUMIN DERIVATIVES AND THEIR PHARMACEUTICAL USES THEREOF UNIVERSITY OF ROCHESTER (US) 2009-02-05 WO disclosed
US-20070219187-A1 Allosteric Modulators of Metabotropic Glutamate Receptors ADDEX PHARMA SA (CH) 2007-09-20 US disclosed
EP-1070708-B1 Triazole derivatives HOFFMANN LA ROCHE (CH) 2004-01-14 EP disclosed
US-6265426-B1 CENTRAL NERVOUS SYSTEM DISORDERS HOFFMANN-LA ROCHE INC. 2001-07-24 US disclosed
EP-1070708-A1 Triazole and imidazole derivatives F. HOFFMANN-LA ROCHE AG (CH) 2001-01-24 EP disclosed
US-5919799-A OVERCOMING RESISTANCE TO AN ANTI-NEOPLASTIC AGENT OR AN ENHANCER FOR THE EFFECT OF AN ANTI-NEOPLASTIC AGENT COMPRISING SAID ENHANCER FOR THE EFFECT OF AN ANTI-NEOPLASTIC AGENT NIKKEN CHEMICALS CO., LTD. (JP) 1999-07-06 US disclosed
EP-0816366-A1 IMIDAZOTHIAZOLE COMPOUNDS Nikken Chemicals Company, Limited (JP) 1998-01-07 EP disclosed
US-4199588-A TRANQUILIZERS, MUSCLE RELAXANTS, ANTICONVULSANTS BOEHRINGER INGELHEIM GMBH (DE) 1980-04-22 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 (7 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-20070219187-A1 Allosteric Modulators of Metabotropic Glutamate Receptors GRM5, GRM2, GRM1 BCHE 855/4885TSHR 268/4885ALDH1A1 3593/4885
US-20120022108-A1 ALLOSTERIC MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS GRM5, GRM2, GRM1 BCHE 855/4885TSHR 268/4885ALDH1A1 3593/4885
US-20220220117-A1 9-SUBSTITUTED AMINO TRIAZOLO QUINAZOLINE DERIVATIVES AS ADENOSINE RECEPTOR ANTAGONISTS, PHARMACEUTICAL COMPOSITIONS AND THEIR USE ADORA2A, ADORA2B, ADORA3 BCHE 3801/4885TSHR 131/4885ALDH1A1 815/4885
US-12060357-B2 9-substituted amino triazolo quinazoline derivatives as adenosine receptor antagonists, pharmaceutical compositions and their use ADORA2A, ADORA2B, ADORA3 BCHE 3801/4885TSHR 131/4885ALDH1A1 815/4885
US-20180222895-A1 COMPOUNDS FOR USE IN PREPARING HETEROCYCLIC TRIAZOLE AGONISTS OF THE APJ RECEPTOR TBXA2R, APLNR, GPR27 BCHE 4453/4885TSHR 262/4885ALDH1A1 2981/4885
US-10150760-B2 Compounds for use in preparing heterocyclic triazole agonists of the APJ receptor TBXA2R, APLNR, GPR27 BCHE 4453/4885TSHR 262/4885ALDH1A1 2981/4885
US-20170320860-A1 HETEROCYCLIC TRIAZOLE COMPOUNDS AS AGONISTS OF THE APJ RECEPTOR TBXA2R, APLNR, AGTR1 BCHE 4679/4885TSHR 225/4885ALDH1A1 2192/4885

“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.