SCHEMBL4371563

SCHEMBL4371563

Fc1cc(C(F)(F)F)cnc1Cl

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 7/20 0.46
POLB P06746 2/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
PLAU P00749 1/20 0.43
KDM4E B2RXH2 1/20 0.43
HTT P42858 3/20 0.41
GAA P10253 2/20 0.41
TDP1 Q9NUW8 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.40
MAPT P10636 2/20 0.39
LMNA P02545 1/20 0.39
GLA P06280 1/20 0.39
HPGD P15428 1/20 0.39
KMT2A Q03164 1/20 0.39
NPSR1 Q6W5P4 1/20 0.38
NPC1 O15118 1/20 0.38
RAB9A P51151 1/20 0.38
MAPK1 P28482 1/20 0.38
PKM P14618 1/20 0.38
AHR P35869 1/20 0.38

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
SCHEMBL30062543 1.00 ALDH1A1 (0.46) ALDH1A1POLBSMN1; SMN2PLAUKDM4E
SCHEMBL9255319 0.83 TSHR (0.32) ALDH1A1HTTGAA
SCHEMBL6371294 0.81 ALOX5AP (0.39) ALDH1A1POLBL3MBTL1LMNARAB9A
SCHEMBL120994 0.80 ALDH1A1 (0.56) ALDH1A1POLBSMN1; SMN2PLAUKDM4E
SCHEMBL29414916 0.80 ALDH1A1 (0.56) ALDH1A1POLBSMN1; SMN2PLAUKDM4E
SCHEMBL30144074 0.78 AGBL2 (0.47) ALDH1A1POLBSMN1; SMN2PLAUKDM4E
SCHEMBL8408164 0.78 PIK3CD (0.50) ALDH1A1POLBSMN1; SMN2PLAUKDM4E
SCHEMBL753475 0.78 AGBL2 (0.47) ALDH1A1POLBSMN1; SMN2PLAUKDM4E
SCHEMBL31310688 0.78 PIK3CD (0.50) ALDH1A1POLBSMN1; SMN2PLAUKDM4E
SCHEMBL609041 0.77 ALDH1A1 (0.40) ALDH1A1POLBSMN1; SMN2PLAUKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250059166-A1 PIPERIDINYLPYRIDINYLCARBONITRILE DERIVATIVES AS INHIBITORS OF GLUTAMINYL-PEPTIDE CYCLOTRANSFERASE AND GLUTAMINYL-PEPTIDE CYCLOTRANSFERASE LIKE PROTEIN BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2025-02-20 US disclosed
US-12226405-B2 Compounds and compositions for inhibiting the activity of HIF2-alpha and their methods of use NOVARTIS AG (CH) 2025-02-18 US disclosed
US-20240351997-A1 NOVEL PARP7 INHIBITOR AND USE THEREOF SHANGHAI QILU PHARMACEUTICAL RESEARCH AND DEVELOPMENT CENTRE LTD. (CN) 2024-10-24 US disclosed
EP-4378938-A1 NOVEL PARP7 INHIBITOR AND USE THEREOF Shanghai Qilu Pharmaceutical Research and Development Centre Ltd. (CN) 2024-06-05 EP disclosed
EP-4143187-B1 COMPOUNDS AND COMPOSITIONS FOR INHIBITING THE ACTIVITY OF HIF2-ALPHA AND THEIR METHODS OF USE NOVARTIS AG (CH) 2024-05-08 EP disclosed
CN-117642393-A Novel PARP7 inhibitor and application thereof 上海齐鲁制药研究中心有限公司 2024-03-01 CN disclosed
EP-4143187-A1 COMPOUNDS AND COMPOSITIONS FOR INHIBITING THE ACTIVITY OF HIF2-ALPHA AND THEIR METHODS OF USE Novartis AG (CH) 2023-03-08 EP disclosed
WO-2023006013-A1 NOVEL PARP7 INHIBITOR AND USE THEREOF 上海齐鲁制药研究中心有限公司 2023-02-02 WO disclosed
US-20220401422-A1 COMPOUNDS AND COMPOSITIONS FOR INHIBITING THE ACTIVITY OF HIF2-alpha AND THEIR METHODS OF USE NOVARTIS AG (CH) 2022-12-22 US disclosed
CN-115485275-A Compounds and compositions that inhibit HIF 2-alpha activity and methods of use thereof 诺华股份有限公司 2022-12-16 CN disclosed
EP-0178260-A2 Process for the preparation of fluorinated pyridine derivatives CIBA-GEIGY AG (CH) 1986-04-16 EP disclosed
US-4567274-A TRICHLOROMETHYL OR DICHLORFLUOROMETHLPICOLINE THE DOW CHEMICAL COMPANY (US) 1986-01-28 US disclosed
US-4565568-A Pyridyl(oxy/thio)phenoxy compounds, herbicidal compositions and methods THE DOW CHEMICAL COMPANY (US) 1986-01-21 US disclosed
US-4480102-A 2,3-Difluoro-5-(trifluoromethyl)pyridine and methods of making and using the same THE DOW CHEMICAL COMPANY (US) 1984-10-30 US disclosed
EP-0104715-A2 2,3-Difluoro-5-(trifluoromethyl)pyridine and method of making and using the same THE DOW CHEMICAL COMPANY (US) 1984-04-04 EP disclosed
EP-0097460-A1 Pyridyl(oxy/thio)phenoxy compounds, herbicidal compositions and methods THE DOW CHEMICAL COMPANY (US) 1984-01-04 EP disclosed
US-4393212-A ADRENERGIC BLOCKING AGENTS MERCK & CO., INC. (US) 1983-07-12 US disclosed
US-4294969-A COUPLING N-BROMOSUCCINIMIDE AND A 2-BROMOPYRIDINE MERCK & CO., INC. (US) 1981-10-13 US disclosed
US-4279913-A ANTIARRYTHMIA, HYPOTENSIVE MERCK & CO., INC. (US) 1981-07-21 US disclosed
EP-0003278-A1 Polysubstituted-2-(3-loweralkylamino-2-R0-propoxy)pyridines, process for preparing the same, and pharmaceutical compositions containing the same MERCK & CO. INC. (US) 1979-08-08 EP 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-12226405-B2 Compounds and compositions for inhibiting the activity of HIF2-alpha and their methods of use HIF1AN, HIF1A, EGLN2 ALDH1A1 450/4885POLB 945/4885SMN1; SMN2 1776/4885
US-20220401422-A1 COMPOUNDS AND COMPOSITIONS FOR INHIBITING THE ACTIVITY OF HIF2-alpha AND THEIR METHODS OF USE HIF1AN, HIF1A, EGLN2 ALDH1A1 450/4885POLB 945/4885SMN1; SMN2 1776/4885
US-20250059166-A1 PIPERIDINYLPYRIDINYLCARBONITRILE DERIVATIVES AS INHIBITORS OF GLUTAMINYL-PEPTIDE CYCLOTRANSFERASE AND GLUTAMINYL-PEPTIDE CYCLOTRANSFERASE LIKE PROTEIN QPCT, QPCTL, GLUL ALDH1A1 3857/4885POLB 844/4885SMN1; SMN2 4484/4885
US-20240351997-A1 NOVEL PARP7 INHIBITOR AND USE THEREOF PARP6, PARP4, PARP3 ALDH1A1 549/4885POLB 197/4885SMN1; SMN2 3311/4885

“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.