SCHEMBL480208

SCHEMBL480208

COc1cc(Cl)c(CBr)cc1F

nearest known ligand 0.45

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
HTR2A P28223 12/20 0.43
SLC6A4 P31645 2/20 0.43
KCNH2 Q12809 2/20 0.43
TAAR1 Q96RJ0 1/20 0.43
HTR2C P28335 10/20 0.41
HTR2B P41595 10/20 0.41
MAPT P10636 2/20 0.35
MEN1 O00255 1/20 0.35
KMT2A Q03164 1/20 0.35
HTR1A P08908 1/20 0.34

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
SCHEMBL31021691 0.85 HTR2A (0.48) HTR2ASLC6A4KCNH2TAAR1HTR2C
SCHEMBL3390630 0.84 TAAR1 (0.48) HTR2ASLC6A4KCNH2TAAR1HTR2C
SCHEMBL15888289 0.82 TAAR1 (0.52) HTR2ATAAR1HTR2CHTR2BMAPT
SCHEMBL11844278 0.82 TAAR1 (0.47) HTR2ATAAR1HTR2CHTR2BHTR1A
SCHEMBL3775780 0.82 HTR2A (0.41) HTR2ASLC6A4KCNH2TAAR1HTR2C
SCHEMBL5104667 0.81 PDE4A (0.46) HTR2ASLC6A4KCNH2TAAR1HTR2C
SCHEMBL3227013 0.79 HTR2A (0.46) HTR2ATAAR1HTR2C
SCHEMBL25219237 0.79 HTR2A (0.43) HTR2ATAAR1HTR2CHTR2BHTR1A
SCHEMBL16068899 0.79 TAAR1 (0.52) HTR2ATAAR1HTR2CHTR2BMAPT
SCHEMBL6738129 0.78 TAAR1 (0.51) HTR2ATAAR1HTR2CHTR2BMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8883786-B2 Glucocorticoid receptor antagonists HOFFMANN-LA ROCHE INC. (US) 2014-11-11 US disclosed
EP-2411361-B1 1,1,1-TRIFLUORO-2-HYDROXYPROPYL COMPOUNDS HOFFMANN LA ROCHE (CH) 2014-06-18 EP disclosed
US-20130045972-A1 GLUCOCORTICOID RECEPTOR ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2013-02-21 US disclosed
US-8143280-B2 Glucocorticoid receptor antagonists HOFFMANN-LA ROCHE INC. (US) 2012-03-27 US disclosed
US-8138189-B2 Substituted benzene compounds as modulators of the glucocorticoid receptor HOFFMAN-LA ROCHE INC. (US) 2012-03-20 US disclosed
EP-2411361-A1 1,1,1-TRIFLUORO-2-HYDROXYPROPYL COMPOUNDS F. Hoffmann-La Roche AG (CH) 2012-02-01 EP disclosed
EP-2205562-B1 1,1,1-TRIFLUORO-2-HYDROXY-3-PHENYLPROPANE DERIVATIVES HOFFMANN LA ROCHE (CH) 2011-03-16 EP disclosed
US-20100249139-A1 1,1,1-TRIFLUORO-2-HYDROXYPROPYL COMPOUNDS HOFFMANN-LA ROCHE, INC. 2010-09-30 US disclosed
WO-2010108902-A1 1,1,1-TRIFLUORO-2-HYDROXYPROPYL COMPOUNDS F. HOFFMANN-LA ROCHE AG (CH) 2010-09-30 WO disclosed
EP-2205562-A1 1,1,1-TRIFLUORO-2-HYDROXY-3-PHENYLPROPANE DERIVATIVES F. Hoffmann-Roche AG (CH) 2010-07-14 EP disclosed
US-7442792-B2 halogenation of pyrazolo[1,5-a][1,3,5]triazin-4-ol's, with phosphorus oxyhalides, then dehalogenation and amination to yield dimethylpyrazolo[1,5-a][1,3,5]triazin-4-amine's, used as corticotropin releasing factor (CRF) receptor antagonists; anxiolytic agents; antidepressants BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2008-10-28 US disclosed
US-20070161790-A1 Process for the preparation of pyrazolo[1,5-a]-1,3,5-triazines and intermediates thereof BRISTOL-MYERS SQUIBB PHARMA COMPANY 2007-07-12 US disclosed
US-20070161790-A1 Process for the preparation of pyrazolo[1,5-a]-1,3,5-triazines and intermediates thereof BRISTOL-MYERS SQUIBB PHARMA COMPANY 2007-07-12 US disclosed
US-20070161790-A1 Process for the preparation of pyrazolo[1,5-a]-1,3,5-triazines and intermediates thereof BRISTOL-MYERS SQUIBB PHARMA COMPANY 2007-07-12 US disclosed
US-7208596-B2 Processes for the preparation of pyrazolo[1,5-a]-1,3,5-triazines and intermediates thereof BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2007-04-24 US disclosed
US-7208596-B2 Processes for the preparation of pyrazolo[1,5-a]-1,3,5-triazines and intermediates thereof BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2007-04-24 US disclosed
US-7208596-B2 Processes for the preparation of pyrazolo[1,5-a]-1,3,5-triazines and intermediates thereof BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2007-04-24 US disclosed
EP-1706408-A2 PROCESSES FOR THE PREPARATION OF PYRAZOLO[1,5- A] -1,3,5-TRIAZINES AND INTERMEDIATES THEREOF Bristol-Myers Squibb Pharma Company (US) 2006-10-04 EP disclosed
US-20050143380-A1 Processes for the preparation of pyrazolo[1,5-a]-1,3,5-triazines and intermediates thereof BRISTOL-MYERS SQUIBB PHARMA COMPANY 2005-06-30 US disclosed
WO-2005051954-A2 PROCESSES FOR THE PREPARATION OF PYRAZOLO[1,5-a]-1,3,5-TRIAZINES AND INTERMEDIATES THEREOF BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2005-06-09 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 (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-20100249139-A1 1,1,1-TRIFLUORO-2-HYDROXYPROPYL COMPOUNDS NR3C1, NR3C2, CRHR1 HTR2A 101/4885SLC6A4 525/4885KCNH2 2332/4885
US-20070161790-A1 Process for the preparation of pyrazolo[1,5-a]-1,3,5-triazines and intermediates thereof CRHR1, CRH, CRHR2 HTR2A 31/4885SLC6A4 796/4885KCNH2 3247/4885
US-20130045972-A1 GLUCOCORTICOID RECEPTOR ANTAGONISTS NR3C1, NR3C2, MC2R HTR2A 176/4885SLC6A4 784/4885KCNH2 1967/4885
US-20050143380-A1 Processes for the preparation of pyrazolo[1,5-a]-1,3,5-triazines and intermediates thereof CRHR1, CRH, CRHR2 HTR2A 37/4885SLC6A4 744/4885KCNH2 3321/4885

“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.