SCHEMBL9974258

SCHEMBL9974258

BCc1ccc(F)c(F)c1

nearest known ligand 0.45

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
▸ HTT P42858 2/20 0.45
▸ ALDH1A1 P00352 1/20 0.45
▸ CYP17A1 P05093 1/20 0.39
▸ CYP11B1 P15538 1/20 0.39
▸ CYP11B2 P19099 1/20 0.39
▸ DAO P14920 4/20 0.39
▸ MAOA P21397 1/20 0.37
▸ MAOB P27338 1/20 0.37
▸ RIPK1 Q13546 1/20 0.36
▸ KDM1A O60341 1/20 0.36
▸ CES2 O00748 1/20 0.36
▸ CES1 P23141 1/20 0.36
▸ MPO P05164 1/20 0.33

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
SCHEMBL13906257 0.78 PIK3CA (0.44) HTTALDH1A1DAOMAOB
SCHEMBL3299911 0.78 CYP17A1 (0.52) HTTALDH1A1CYP17A1CYP11B1CYP11B2
SCHEMBL16105820 0.78 DAO (0.55) HTTALDH1A1CYP17A1CYP11B1CYP11B2
SCHEMBL28041389 0.76 HTT (0.47) HTTALDH1A1CYP17A1CYP11B1CYP11B2
SCHEMBL6203927 0.76 HTT (0.47) HTTALDH1A1CYP17A1CYP11B1CYP11B2
SCHEMBL1300421 0.75 HTT (0.42) HTTALDH1A1CYP17A1CYP11B1CYP11B2
Hydrochloric Acid SCHEMBL2823747 0.74 HTT (0.45) HTTALDH1A1CYP17A1CYP11B1CYP11B2
SCHEMBL110823 0.74 LOXL2 (0.52) HTTALDH1A1CYP17A1CYP11B1CYP11B2
Iodide SCHEMBL2215328 0.74 HTT (0.45) HTTALDH1A1CYP17A1CYP11B1CYP11B2
SCHEMBL17552652 0.74 HTT (0.45) HTTALDH1A1CYP17A1CYP11B1CYP11B2

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 7 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2562162-A1 5-FLUORO PYRIMIDINE DERIVATIVES AS FUNGICIDES Dow AgroSciences LLC (US) 2013-02-27 — — EP disclosed
US-20120157691-A1 Lewis Acid Catalyzed Halogenation of Activated Carbon Atoms JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) 2012-06-21 — — US disclosed
EP-2272832-A1 PHENYLPROPIONIC ACID DERIVATIVE AND USE THEREOF Asahi Kasei Pharma Corporation (JP) 2011-01-12 — — EP disclosed
WO-2009134616-A2 NOVEL INHIBITORS OF HEPATITIS C VIRUS REPLICATION INTERMUNE, INC. (US) 2009-11-05 — — WO disclosed
US-20080275253-A1 halogenation with a halogen donor selected from N-bromosuccinimide, N-iodosuccinimide, N-chlorosuccinimide and N-fluorobenzene-sulfonimide, 1,3-dibromo-5,5-dimethyl imidazolidine-2,4-dione in presence of ZrCl4; bromination of tetramethylsilane JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) 2008-11-06 — — US disclosed
WO-2008058536-A1 NOVEL 4-AMINO-PYRIDINE DERIVATIVES AND THEIR USE AS POTASSIUM CHANNEL MODULATORS NEUROSEARCH A/S (DK) 2008-05-22 — — WO disclosed
WO-2008058537-A1 NOVEL 2-AMINO-PYRIDINE DERIVATIVES AND THEIR USE AS POTASSIUM CHANNEL MODULATORS NEUROSEARCH A/S (DK) 2008-05-22 — — 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 (2 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-20080275253-A1 halogenation with a halogen donor selected from N-bromosuccinimide, N-iodosuccinimide, N-chlorosuccinimide and N-fluorobenzene-sulfonimide, 1,3-dibromo-5,5-dimethyl imidazolidine-2,4-dione in presence of ZrCl4; bromination of tetramethylsilane HDHD5, ZRANB2, CLIC4 HTT 3950/4885ALDH1A1 2847/4885CYP17A1 4756/4885
US-20120157691-A1 Lewis Acid Catalyzed Halogenation of Activated Carbon Atoms NBAS, CA3, CA9 HTT 3369/4885ALDH1A1 2972/4885CYP17A1 4221/4885

“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.

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