SCHEMBL1074604

SCHEMBL1074604

CCCCCc1nccnc1CCCCC

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 1/20 0.47
L3MBTL1 Q9Y468 1/20 0.47
KCNH2 Q12809 1/20 0.41
MEN1 O00255 1/20 0.38
KMT2A Q03164 1/20 0.38
PTGS2 P35354 4/20 0.38
CYP3A4 P08684 3/20 0.38
CYP2D6 P10635 1/20 0.38
KDM4E B2RXH2 2/20 0.37
TLR7 Q9NYK1 1/20 0.37
ESR1 P03372 2/20 0.37
ADRA2A P08913 2/20 0.37
ADORA3 P0DMS8 2/20 0.37
TACR2 P21452 2/20 0.37
SLC6A2 P23975 2/20 0.37
SLC6A4 P31645 2/20 0.37
SLC6A3 Q01959 2/20 0.37
ALDH1A1 P00352 1/20 0.37
LMNA P02545 1/20 0.37
SHBG P04278 1/20 0.37

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
SCHEMBL27818098 0.97 TDP1 (0.45) TDP1L3MBTL1KCNH2MEN1KMT2A
SCHEMBL30665021 0.86 TDP1 (0.41) TDP1L3MBTL1KCNH2MEN1KMT2A
SCHEMBL293479 0.86 TDP1 (0.41) TDP1L3MBTL1KCNH2MEN1KMT2A
SCHEMBL293478 0.84 TDP1 (0.40) TDP1L3MBTL1KCNH2MEN1KMT2A
SCHEMBL27862457 0.84 PTGS2 (0.41) TDP1L3MBTL1KCNH2PTGS2CYP3A4
SCHEMBL10496018 0.84 TDP1 (0.40) TDP1L3MBTL1KCNH2PTGS2CYP3A4
SCHEMBL6753235 0.84 TLR7 (0.46) TDP1L3MBTL1KCNH2MEN1KMT2A
SCHEMBL14776060 0.84 L3MBTL1 (0.40) TDP1L3MBTL1KCNH2MEN1KMT2A
SCHEMBL22623929 0.83 TDP1 (0.39) TDP1L3MBTL1KCNH2MEN1KMT2A
SCHEMBL1033248 0.81 ALDH1A1 (0.40) TDP1L3MBTL1KCNH2MEN1KMT2A

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
EP-0256839-B1 SMOKING COMPOSITIONS CONTAINING A FLAVORANT ADDITIVE Philip Morris Products Inc. (US) 1991-11-06 EP claimed
CN-104672152-B Organic compound and its application in the synthesis of organometallic complex 株式会社半导体能源研究所 2018-09-21 CN disclosed
CN-101267838-B Use of DPP-IV inhibitors to reduce hypoglycemic events NOVARTIS AG 2012-09-05 CN disclosed
WO-2011000481-A1 SYNTHESIS OF PYRAZINE DERIVATES MERCK PATENT GMBH (DE) 2011-01-06 WO disclosed
CN-101267838-A Use of DPP-IV inhibitors to reduce hypoglycemic events NOVARTIS AG (CH) 2008-09-17 CN disclosed
CN-101222919-A Combination of a DPP-iv inhibitor and a cannabinoid CB1 receptor antagonist NOVARTIS AG (CH) 2008-07-16 CN disclosed
EP-1871762-A2 SUBTITUTED HETEROARYL CB1 ANTAGONISTS NEUROGEN CORPORATION (US) 2008-01-02 EP disclosed
US-20070093505-A1 2,3-Substituted 5,6-diaryl-pyrazine derivatives as cb1 modulators ASTRAZENECA AB (SE) 2007-04-26 US disclosed
US-20070078135-A1 Substituted heteroaryl CB1 antagonists NEUROGEN CORPORATION (US) 2007-04-05 US disclosed
CN-1867332-A Comprising a selective CB1Combination therapy of obesity with antagonists and lipase inhibitors SOLVAY PHARM GMBH (DE) 2006-11-22 CN disclosed
US-6887875-B2 Bind with high selectivity and/ or high affinity to CRF1 receptors (Corticotropin Releasing Factor 1 Receptors), useful for treating psychiatric and neurological diseases, including depression, anxiety and post trauma stress NEUROGEN CORPORATION (US) 2005-05-03 US disclosed
EP-1399428-A1 2,5-DIARYLPYRAZINES, 2,5-DIARYLPYRIDINES AND 2,5-DIARYLPYRIMIDINES AS CRF1 RECEPTOR MODULATORS Neurogen Corporation (US) 2004-03-24 EP disclosed
EP-1399428-A1 2,5-DIARYLPYRAZINES, 2,5-DIARYLPYRIDINES AND 2,5-DIARYLPYRIMIDINES AS CRF1 RECEPTOR MODULATORS Neurogen Corporation (US) 2004-03-24 EP disclosed
US-20030119844-A1 2,5-diarylpyrazines, 2,5-diarylpyridines and 2,5-diarylpyrimidines NEUROGEN CORPORATION 2003-06-26 US disclosed
US-20030119844-A1 2,5-diarylpyrazines, 2,5-diarylpyridines and 2,5-diarylpyrimidines NEUROGEN CORPORATION 2003-06-26 US disclosed
WO-2002100838-A1 2,5-DIARYLPYRAZINES, 2,5-DIARYLPYRIDINES AND 2,5-DIARYLPYRIMIDINES AS CRF1 RECEPTOR MODULATORS NEUROGEN CORPORATION (US) 2002-12-19 WO disclosed
WO-2002100838-A1 2,5-DIARYLPYRAZINES, 2,5-DIARYLPYRIDINES AND 2,5-DIARYLPYRIMIDINES AS CRF1 RECEPTOR MODULATORS NEUROGEN CORPORATION (US) 2002-12-19 WO disclosed
US-20020161528-A1 Tool for lipophilicity determination in drug discovery basic and neutral compounds PFIZER INC. 2002-10-31 US disclosed
EP-1239280-A2 ElogDoct:A tool for lipophilicity determination in drug discovery basic and neutral compounds Pfizer Products Inc. (US) 2002-09-11 EP disclosed
US-4513135-A GAMMA-AMINOBUTYRIC ACID BINDING AGTIVATORS ELI LILLY AND COMPANY (US) 1985-04-23 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 (3 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-20030119844-A1 2,5-diarylpyrazines, 2,5-diarylpyridines and 2,5-diarylpyrimidines CRHR2, CRHR1, CRH TDP1 966/4885L3MBTL1 4409/4885KCNH2 4424/4885
US-20070093505-A1 2,3-Substituted 5,6-diaryl-pyrazine derivatives as cb1 modulators CNR2, CNR1, HTR2C TDP1 4119/4885L3MBTL1 4181/4885KCNH2 1287/4885
US-20070078135-A1 Substituted heteroaryl CB1 antagonists CNR1, CNR2, OPRL1 TDP1 4381/4885L3MBTL1 2120/4885KCNH2 3509/4885

“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.