SCHEMBL2387153

SCHEMBL2387153

CCOc1ncccc1C(F)(F)F

nearest known ligand 0.48

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
SLC22A12 Q96S37 1/20 0.46
SSTR4 P31391 10/20 0.44
SSTR1 P30872 4/20 0.44
ALDH1A1 P00352 1/20 0.43
MAPT P10636 1/20 0.43
ATM Q13315 1/20 0.43
NFE2L2 Q16236 1/20 0.42
HTR1A P08908 1/20 0.42
SLC6A2 P23975 1/20 0.42
SLC6A4 P31645 1/20 0.42
SLC6A3 Q01959 1/20 0.42

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
SCHEMBL15677613 0.86 SLC22A12 (0.44) SLC22A12SSTR4SSTR1ALDH1A1MAPT
SCHEMBL16579444 0.84 ALDH1A1 (0.44) SLC22A12SSTR4SSTR1ALDH1A1MAPT
SCHEMBL12922790 0.83 MEN1 (0.42) ALDH1A1SLC6A2
SCHEMBL19002316 0.82 SSTR4 (0.51) SLC22A12SSTR4SSTR1
SCHEMBL30115270 0.82 SMN1; SMN2 (0.39) SLC22A12SSTR4SSTR1HTR1ASLC6A2
SCHEMBL29213683 0.81 GAA (0.42) ALDH1A1ATMSLC6A2SLC6A4
SCHEMBL30440802 0.81 SLC22A12 (0.55) SLC22A12ALDH1A1MAPTATMNFE2L2
SCHEMBL322870 0.81 SLC22A12 (0.55) SLC22A12ALDH1A1MAPTATMNFE2L2
SCHEMBL2825181 0.80 KDM4E (0.53) SSTR4SSTR1ALDH1A1
SCHEMBL23886163 0.80 SSTR4 (0.49) SLC22A12SSTR4SSTR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12319683-B2 Azabenzimidazole compounds and pharmaceutical NIPPON SHINYAKU CO., LTD. (JP) 2025-06-03 US disclosed
CN-112441966-A Method for producing 2-chloro-3-trifluoromethylpyridine from 2,3, 6-trichloro-5-trifluoromethylpyridine 山东省农药科学研究院 2021-03-05 CN disclosed
US-20190055257-A1 SUBSTITUTED 6,7-DIHYDROPYRAZOLO[1,5-a]PYRAZINES AS NEGATIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS JANSSEN PHARMACEUTICA NV (BE) 2019-02-21 US disclosed
EP-3233077-A1 DOPAMINE D2 RECEPTOR LIGANDS The Broad Institute Inc. (US) 2017-10-25 EP disclosed
EP-3004107-B1 6,7-DIHYDROPYRAZOLO[1,5-A]PYRAZIN-4(5H)-ONE COMPOUNDS AND THEIR USE AS NEGATIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS JANSSEN PHARMACEUTICA NV (BE) 2017-05-10 EP disclosed
WO-2016100940-A1 DOPAMINE D2 RECEPTOR LIGANDS THE BROAD INSTITUTE, INC. (US) 2016-06-23 WO disclosed
US-8013001-B2 Modulators of LXR EXELIXIS, INC. (US) 2011-09-06 US disclosed
US-20100056582-A1 Modulators of LXR X-CEPTOR THERAPEUTICS, INC. (US) 2010-03-04 US disclosed
EP-1811845-A4 SUBSTITUTED BIARYL QUINOLIN-4-YLAMINE ANALOGUES NEUROGEN CORP (US) 2009-07-15 EP disclosed
US-7482366-B2 Modulators of LXR X-CEPTOR THERAPEUTICS, INC. (US) 2009-01-27 US disclosed
US-20080071084-A1 Using an alcohol in presence of copper catalyst and ligand ARCHIMICA GMBH (DE) 2008-03-20 US disclosed
US-20080071084-A1 Using an alcohol in presence of copper catalyst and ligand ARCHIMICA GMBH (DE) 2008-03-20 US disclosed
EP-1873136-A1 Method for manufacturing alkyl and aryl ethers Archimica GmbH (DE) 2008-01-02 EP disclosed
EP-1873136-A1 Method for manufacturing alkyl and aryl ethers Archimica GmbH (DE) 2008-01-02 EP disclosed
EP-1811845-A2 SUBSTITUTED BIARYL QUINOLIN-4-YLAMINE ANALOGUES NEUROGEN CORPORATION (US) 2007-08-01 EP disclosed
EP-1773337-A2 MODULATORS OF NUCLEAR RECEPTORS Exelixis, Inc. (US) 2007-04-18 EP disclosed
WO-2006042289-A2 SUBSTITUTED BIARYL QUINOLIN-4-YLAMINE ANALOGUES NEUROGEN CORPORATION (US) 2006-04-20 WO disclosed
WO-2006025979-A9 MODULATORS OF NUCLEAR RECEPTORS EXELIXIS INC (US) 2006-04-20 WO disclosed
WO-2006025979-A2 MODULATORS OF NUCLEAR RECEPTORS EXELIXIS, INC. (US) 2006-03-09 WO disclosed
US-20050080111-A1 Modulators of LXR X-CEPTOR THERAPEUTICS, INC. (US) 2005-04-14 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 (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-20050080111-A1 Modulators of LXR NR1H2, NR1H3, NR1H4 SLC22A12 1905/4885SSTR4 1340/4885SSTR1 1114/4885
US-20080071084-A1 Using an alcohol in presence of copper catalyst and ligand NR1H3, NR1H2, ADH1A SLC22A12 2841/4885SSTR4 1924/4885SSTR1 790/4885
US-20190055257-A1 SUBSTITUTED 6,7-DIHYDROPYRAZOLO[1,5-a]PYRAZINES AS NEGATIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS GRM2, GRM5, GRM1 SLC22A12 967/4885SSTR4 1983/4885SSTR1 1111/4885
US-20100056582-A1 Modulators of LXR NR1H2, NR1H3, NR1H4 SLC22A12 1905/4885SSTR4 1340/4885SSTR1 1114/4885
US-12319683-B2 Azabenzimidazole compounds and pharmaceutical PAM, CHRM3, AZI2 SLC22A12 1322/4885SSTR4 1340/4885SSTR1 1410/4885

“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.