SCHEMBL508482

SCHEMBL508482

COc1cc(Cl)cc(C#N)c1

nearest known ligand 0.46

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.46
KCNH2 Q12809 1/20 0.46
MAPT P10636 1/20 0.40
KMT2A Q03164 1/20 0.40
HPGDS O60760 1/20 0.38
GRM5 P41594 1/20 0.38
ACLY P53396 1/20 0.37
KDM1A O60341 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
SCHEMBL13119716 0.94 KCNH2 (0.49) ALDH1A1KCNH2MAPTKMT2A
SCHEMBL13140960 0.90 KCNH2 (0.46) ALDH1A1KCNH2MAPTKMT2A
SCHEMBL13119742 0.88 KCNH2 (0.45) ALDH1A1KCNH2MAPTKMT2A
SCHEMBL202404 0.87 ALDH1A1 (0.61) ALDH1A1HPGDSGRM5KDM1A
SCHEMBL509576 0.84 ALDH1A1 (0.58) ALDH1A1HPGDSGRM5KDM1A
SCHEMBL13586642 0.84 KCNH2 (0.51) KCNH2MAPTKMT2A
SCHEMBL3600097 0.82 AR (0.46) KCNH2MAPTKMT2A
SCHEMBL21263 0.82 ALDH1A1 (0.69) ALDH1A1
Ammonia Solution, Strong SCHEMBL3944394 0.81 ALDH1A1 (0.48) ALDH1A1HPGDSGRM5KDM1A
SCHEMBL3160328 0.81 CYP3A4 (0.50) KCNH2MAPTKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3785714-A1 PRODRUGS OF HIV REVERSE TRANSCRIPTASE INHIBITORS MERCK SHARP & DOHME CORP. (US) 2021-03-03 EP disclosed
EP-3125894-B1 PRODRUGS OF HIV REVERSE TRANSCRIPTASE INHIBITORS MERCK SHARP & DOHME (US) 2020-09-09 EP disclosed
EP-3656384-A1 COMBINATIONS COMPRISING 5-PHENOXY-3H-PYRIMIDIN-4-ONE DERIVATIVES AND THEIR USE FOR THE PROPHYLAXIS OR TREATMENT OF INFECTION BY HIV MERCK SHARP & DOHME CORP. (US) 2020-05-27 EP disclosed
US-10562912-B2 Heterocyclic derivatives and use thereof C&C RESEARCH LABORATORIES (KR) 2020-02-18 US disclosed
EP-3004057-B1 HETEROCYCLIC DERIVATIVES AND THEIR USE AS STAT 3 INHIBITORS C&C RES LAB (KR) 2018-07-25 EP disclosed
EP-3295942-A1 COMBINATIONS COMPRISING 5-PHENOXY-3H-PYRIMIDIN-4-ONE DERIVATIVES AND THEIR USE FOR THE PROPHYLAXIS OR TREATMENT OF INFECTION BY HIV MERCK SHARP & DOHME CORP. (US) 2018-03-21 EP disclosed
EP-2903977-B1 5-PHENOXY-3H-PYRIMIDIN-4-ONE DERIVATIVES AND THEIR USE AS HIV REVERSE TRANSCRIPTASE INHIBITORS MERCK SHARP & DOHME (US) 2017-09-20 EP disclosed
US-9695166-B2 Pyrazolopyridine pyrazolopyrimidine and related compounds GLOBAL BLOOD THERAPEUTICS, INC. (US) 2017-07-04 US disclosed
US-9598397-B2 Process for making reverse transcriptase inhibitors MERCK SHARP & DOHME CORP. (US) 2017-03-21 US disclosed
US-9550757-B2 Nuclear transport modulators and uses thereof Karyopharm Therapeutics Inc. (US) 2017-01-24 US disclosed
EP-1608629-A1 BENZYL-PYRIDAZINONS AS REVERSE TRANSCRIPTASE INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2005-12-28 EP disclosed
WO-2005100323-A1 PROCESS FOR PREPARING PYRIDAZINONE COMPOUNDS F. HOFFMANN-LA ROCHE AG (CH) 2005-10-27 WO disclosed
US-20050234236-A1 Process for preparing pyridazinone compounds ROCHE PALO ALTO LLC 2005-10-20 US disclosed
US-6933312-B2 Pyrazole derivatives AGOURON PHARMACEUTICALS, INC. (US) 2005-08-23 US disclosed
EP-1551828-A1 PYRAZOLE DERIVATIVES Pfizer Limited (GB) 2005-07-13 EP disclosed
US-20040198736-A1 Non-nucleoside reverse transcriptase inhibitors ROCHE PALO ALTO LLC 2004-10-07 US disclosed
WO-2004085406-A1 BENZYL-PYRIDAZINONS AS REVERSE TRANSCRIPTASE INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2004-10-07 WO disclosed
US-20040133002-A1 Pyrazole derivatives PFIZER, INC. 2004-07-08 US disclosed
WO-2004031178-A1 PYRAZOLE DERIVATIVES PFIZER LIMITED (GB) 2004-04-15 WO disclosed
US-20030100554-A1 Pyrazole derivatives JONES LYN HOWARD (GB) 2003-05-29 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-20040133002-A1 Pyrazole derivatives REV1, RRS1, CYP2F1 ALDH1A1 895/4885KCNH2 3181/4885MAPT 2744/4885
US-10562912-B2 Heterocyclic derivatives and use thereof STAT3, JAK2, STAT5A ALDH1A1 1646/4885KCNH2 4785/4885MAPT 4514/4885
US-20040198736-A1 Non-nucleoside reverse transcriptase inhibitors POLR1A, POLR2A, POLR2E ALDH1A1 321/4885KCNH2 3050/4885MAPT 1798/4885
US-20050234236-A1 Process for preparing pyridazinone compounds CYP2A6, CYP2B6, H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16 ALDH1A1 1393/4885KCNH2 1280/4885MAPT 4102/4885
US-20030100554-A1 Pyrazole derivatives REV1, SARS1, CYP2F1 ALDH1A1 385/4885KCNH2 3503/4885MAPT 2150/4885

“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.