SCHEMBL15527832

SCHEMBL15527832

NC(=O)c1ccnc(F)c1F

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 5/20 0.46
ASPH Q12797 1/20 0.46
KDM8 Q8N371 1/20 0.46
L3MBTL1 Q9Y468 2/20 0.43
NAPRT Q6XQN6 1/20 0.42
PARP1 P09874 1/20 0.39
MAPT P10636 2/20 0.38
HTT P42858 1/20 0.38
SIRT3 Q9NTG7 1/20 0.37
TDP1 Q9NUW8 1/20 0.37
DGAT1 O75907 1/20 0.37
LMNA P02545 1/20 0.36
DYRK1B Q9Y463 2/20 0.35
CSNK1A1 P48729 1/20 0.35
TYRO3 Q06418 1/20 0.35
PIK3CB P42338 1/20 0.35
BTK Q06187 1/20 0.34
ALDH1A1 P00352 1/20 0.34
HPGD P15428 1/20 0.34
TSHR P16473 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
SCHEMBL30274664 1.00 KDM4E (0.46) KDM4EASPHKDM8L3MBTL1NAPRT
SCHEMBL14791398 0.83 KDM4E (0.47) KDM4EASPHKDM8L3MBTL1NAPRT
SCHEMBL18417648 0.82 KDM4E (0.44) KDM4EASPHKDM8L3MBTL1NAPRT
SCHEMBL30803051 0.81 KDM4E (0.68) KDM4EASPHKDM8L3MBTL1NAPRT
SCHEMBL3579780 0.81 KDM4E (0.68) KDM4EASPHKDM8L3MBTL1NAPRT
SCHEMBL30881695 0.80 KDM4E (0.43) KDM4EASPHKDM8L3MBTL1PARP1
SCHEMBL17195496 0.80 MKNK1 (0.44) KDM4EASPHKDM8L3MBTL1PARP1
SCHEMBL27747494 0.80 KDM4E (0.41) KDM4EASPHKDM8L3MBTL1NAPRT
SCHEMBL16447580 0.80 SIRT3 (0.43) KDM4EASPHKDM8L3MBTL1NAPRT
SCHEMBL27096669 0.80 KDM4E (0.43) KDM4EASPHKDM8L3MBTL1PARP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12180185-B2 Compound as protein kinase inhibitor, and pharmaceutical composition comprising thereof HK INNO.N CORPORATION (KR) 2024-12-31 US claimed
US-20220009902-A1 NOVEL COMPOUND AS PROTEIN KINASE INHIBITOR, AND PHARMACEUTICAL COMPOSITION COMPRISING THEREOF HK INNO.N CORPORATION (KR) 2022-01-13 US claimed
EP-3261641-A1 PANCREATITIS TREATMENT Calcimedica, Inc. (US) 2018-01-03 EP claimed
WO-2016138472-A1 PANCREATITIS TREATMENT CALCIMEDICA, INC. (US) 2016-09-01 WO claimed
EP-2844655-A1 SUBSTITUTED PYRIDINE COMPOUNDS AS CRAC MODULATORS Lupin Limited (IN) 2015-03-11 EP claimed
WO-2013164769-A1 SUBSTITUTED PYRIDINE COMPOUNDS AS CRAC MODULATORS LUPIN LIMITED (IN) 2013-11-07 WO claimed
US-12329799-B2 Peptidyl inhibitors of calcineurin-NFAT interaction OHIO STATE INNOVATION FOUNDATION (US) 2025-06-17 US disclosed
US-12180185-B2 Compound as protein kinase inhibitor, and pharmaceutical composition comprising thereof HK INNO.N CORPORATION (KR) 2024-12-31 US disclosed
EP-3475275-B1 3-ARYL AND HETEROARYL SUBSTITUTED 5-TRIFLUOROMETHYL OXADIAZOLES AS HISTONE DEACETYLASE 6 (HDAC6) INHIBITORS MERCK SHARP & DOHME LLC (US) 2024-04-10 EP disclosed
US-20240033318-A1 PEPTIDYL INHIBITORS OF CALCINEURIN-NFAT INTERACTION OHIO STATE INNOVATION FOUNDATION 2024-02-01 US disclosed
US-11576946-B2 Peptidyl inhibitors of calcineurin-NFAT interaction OHIO STATE INNOVATION FOUNDATION (US) 2023-02-14 US disclosed
US-20220388979-A1 QUINOLINE DERIVATIVES AS PROTEIN KINASE INHIBITORS B.C.I. PHARMA (BE) 2022-12-08 US disclosed
EP-3131897-B1 FACTOR IXA INHIBITORS MERCK SHARP & DOHME (US) 2022-06-15 EP disclosed
EP-3131896-A1 FACTOR IXA INHIBITORS Merck Sharp & Dohme Corp. (US) 2017-02-22 EP disclosed
US-20170027916-A1 FACTOR IXa INHIBITORS MERCK SHARP & DOHME CORP. (US) 2017-02-02 US disclosed
US-20160168125-A1 WNT SIGNALING INHIBITOR KYOWA HAKKO KIRIN CO., LTD. (JP) 2016-06-16 US disclosed
EP-3028703-A1 Wnt SIGNALING INHIBITOR Kyowa Hakko Kirin Co., Ltd. (JP) 2016-06-08 EP disclosed
WO-2015160634-A1 FACTOR IXA INHIBITORS MERCK SHARP & DOHME CORP. (US) 2015-10-22 WO disclosed
WO-2015160636-A1 FACTOR IXA INHIBITORS MERCK SHARP & DOHME CORP. (US) 2015-10-22 WO disclosed
WO-2014043715-A1 COMPOUNDS THAT MODULATE INTRACELLULAR CALCIUM CALCIMEDICA, INC. (US) 2014-03-20 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 (8 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-20220388979-A1 QUINOLINE DERIVATIVES AS PROTEIN KINASE INHIBITORS ABL1, PHKB, EEF2K KDM4E 1824/4885ASPH 4092/4885KDM8 3315/4885
US-20170027916-A1 FACTOR IXa INHIBITORS F9, F12, TFPI KDM4E 837/4885ASPH 941/4885KDM8 302/4885
US-12329799-B2 Peptidyl inhibitors of calcineurin-NFAT interaction CHP1, NFATC1, PPP3R1 KDM4E 902/4885ASPH 879/4885KDM8 258/4885
US-12180185-B2 Compound as protein kinase inhibitor, and pharmaceutical composition comprising thereof MAP3K20, MAP3K1, MAP3K15 KDM4E 1696/4885ASPH 3301/4885KDM8 1353/4885
US-20240033318-A1 PEPTIDYL INHIBITORS OF CALCINEURIN-NFAT INTERACTION CHP1, NFATC1, PPP3R1 KDM4E 902/4885ASPH 879/4885KDM8 258/4885
US-20220009902-A1 NOVEL COMPOUND AS PROTEIN KINASE INHIBITOR, AND PHARMACEUTICAL COMPOSITION COMPRISING THEREOF MAP3K20, MAP3K1, MAP3K15 KDM4E 1970/4885ASPH 3720/4885KDM8 1788/4885
US-11576946-B2 Peptidyl inhibitors of calcineurin-NFAT interaction CHP1, NFATC1, PPP3R1 KDM4E 902/4885ASPH 879/4885KDM8 258/4885
US-20160168125-A1 WNT SIGNALING INHIBITOR WNT3A, WNT1, WNT3 KDM4E 1585/4885ASPH 913/4885KDM8 2006/4885

“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.