SCHEMBL1699369

SCHEMBL1699369

OB(O)c1ccc(F)c2cccnc12

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 10/20 0.61
L3MBTL1 Q9Y468 5/20 0.61
MPI P34949 1/20 0.61
NPC1 O15118 2/20 0.42
HSP90AA1 P07900 2/20 0.42
SLC40A1 Q9NP59 1/20 0.42
MEN1 O00255 2/20 0.41
IDO1 P14902 2/20 0.41
KMT2A Q03164 2/20 0.41
ALDH1A1 P00352 1/20 0.41
LMNA P02545 1/20 0.41
POLB P06746 1/20 0.41
MAPT P10636 1/20 0.41
THRB P10828 1/20 0.41
PKM P14618 1/20 0.41
RECQL P46063 1/20 0.41
TDO2 P48775 1/20 0.41
BLM P54132 1/20 0.41
CASP6 P55212 1/20 0.41
TDP1 Q9NUW8 1/20 0.41

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
SCHEMBL29698868 1.00 KDM4E (0.61) KDM4EL3MBTL1MPINPC1HSP90AA1
SCHEMBL29953066 0.80 HTT (0.53) KDM4EL3MBTL1MPINPC1HSP90AA1
SCHEMBL10159255 0.80 HTT (0.62) KDM4EL3MBTL1MPINPC1HSP90AA1
SCHEMBL29496213 0.79 SLC40A1 (0.47) KDM4EL3MBTL1MPINPC1HSP90AA1
SCHEMBL10272166 0.79 SLC40A1 (0.47) KDM4EL3MBTL1MPINPC1HSP90AA1
SCHEMBL10159215 0.79 KDM4E (0.61) KDM4EL3MBTL1NPC1HSP90AA1MEN1
SCHEMBL19990071 0.78 KDM4E (0.70) KDM4EL3MBTL1MPINPC1HSP90AA1
SCHEMBL31394891 0.76 KDM4E (0.45) KDM4EL3MBTL1MPINPC1HSP90AA1
SCHEMBL20600794 0.76 KDM4E (0.45) KDM4EL3MBTL1MPINPC1HSP90AA1
SCHEMBL2557719 0.76 L3MBTL1 (0.61) KDM4EL3MBTL1MPINPC1HSP90AA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12441727-B2 Tricyclic compounds as inhibitors of KRAS INCYTE CORPORATION (US) 2025-10-14 US disclosed
US-20250188073-A1 TRICYCLIC COMPOUNDS AS INHIBITORS OF KRAS INCYTE CORP (US) 2025-06-12 US disclosed
EP-4548918-A2 TRICYCLIC COMPOUNDS AS INHIBITORS OF KRAS Incyte Corporation (US) 2025-05-07 EP disclosed
EP-4541422-A2 QUINOLINE DERIVATIVES AS ALPHA4BETA7 INTEGRIN INHIBITORS Gilead Sciences, Inc. (US) 2025-04-23 EP disclosed
CN-119462635-A Quinoline derivatives as alpha 4 beta 7 integrin inhibitors 吉利德科学公司 2025-02-18 CN disclosed
US-20250032473-A1 QUINOLINE DERIVATIVES GILEAD SCIENCES, INC. 2025-01-30 US disclosed
EP-3873884-B1 3-(QUINOLIN-8-YL)-1,4-DIHYDROPYRIDO[3,4-D]PYRIMIDIN-2,4-DIONE DERIVATIVES AS ALPHA4BETA7 INTEGRIN INHIBITORS FOR THE TREATMENT OF INFLAMMATORY DISEASES GILEAD SCIENCES INC (US) 2024-12-04 EP disclosed
CN-112969687-B Quinoline derivatives as a4 b 7 integrin inhibitors 吉利德科学公司 2024-08-23 CN disclosed
US-12053462-B2 Quinoline derivatives GILEAD SCIENCES, INC. (US) 2024-08-06 US disclosed
EP-4367117-A1 TRICYCLIC COMPOUNDS AS INHIBITORS OF KRAS Incyte Corporation (US) 2024-05-15 EP disclosed
US-20200155538-A1 QUINOLINE DERIVATIVES GILEAD SCIENCES, INC. 2020-05-21 US disclosed
US-10450296-B2 Heterocyclic compounds useful as Pim kinase inhibitors INCYTE CORPORATION (US) 2019-10-22 US disclosed
US-20180282302-A1 HETEROCYCLIC COMPOUNDS USEFUL AS PIM KINASE INHIBITORS INCYTE CORPORATION 2018-10-04 US disclosed
US-9920032-B2 Heterocyclic compounds useful as pim kinase inhibitors INCYTE CORPORATION (US) 2018-03-20 US disclosed
EP-2588450-B1 NAPHT-2-YLACETIC ACID DERIVATIVES TO TREAT AIDS GILEAD SCIENCES INC (US) 2017-05-24 EP disclosed
US-20170096411-A1 HETEROCYCLIC COMPOUNDS USEFUL AS PIM KINASE INHIBITORS INCYTE CORPORATION 2017-04-06 US disclosed
US-9102614-B2 Naphth-2-ylacetic acid derivatives to treat AIDS GILEAD SCIENCES, INC. (US) 2015-08-11 US disclosed
US-20130203727-A1 NAPHT-2-YLACETIC ACID DERIVATIVES TO TREAT AIDS GILEAD SCIENCES, INC. (US) 2013-08-08 US disclosed
EP-2588450-A1 NAPHT- 2 -YLACETIC ACID DERIVATIVES TO TREAT AIDS Gilead Sciences, Inc. (US) 2013-05-08 EP disclosed
WO-2012003497-A1 NAPHT- 2 -YLACETIC ACID DERIVATIVES TO TREAT AIDS GILEAD SCIENCES, INC. (US) 2012-01-05 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 (9 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-12441727-B2 Tricyclic compounds as inhibitors of KRAS KRAS, NRAS, HRAS KDM4E 4227/4885L3MBTL1 2692/4885MPI 2577/4885
US-12053462-B2 Quinoline derivatives CFTR, NQO1, IRF3 KDM4E 2522/4885L3MBTL1 4861/4885MPI 2348/4885
US-20180282302-A1 HETEROCYCLIC COMPOUNDS USEFUL AS PIM KINASE INHIBITORS PIM1, PIM2, PIM3 KDM4E 1497/4885L3MBTL1 1056/4885MPI 266/4885
US-20200155538-A1 QUINOLINE DERIVATIVES CFTR, NQO1, IRF3 KDM4E 2522/4885L3MBTL1 4861/4885MPI 2348/4885
US-20250188073-A1 TRICYCLIC COMPOUNDS AS INHIBITORS OF KRAS KRAS, NRAS, HRAS KDM4E 4221/4885L3MBTL1 2885/4885MPI 2662/4885
US-20130203727-A1 NAPHT-2-YLACETIC ACID DERIVATIVES TO TREAT AIDS NFATC1, AADAT, ACAT1 KDM4E 2251/4885L3MBTL1 4008/4885MPI 2418/4885
US-10450296-B2 Heterocyclic compounds useful as Pim kinase inhibitors PIM1, PIM2, PIM3 KDM4E 1497/4885L3MBTL1 1056/4885MPI 266/4885
US-20170096411-A1 HETEROCYCLIC COMPOUNDS USEFUL AS PIM KINASE INHIBITORS PIM1, PIM2, PIM3 KDM4E 1497/4885L3MBTL1 1056/4885MPI 266/4885
US-20250032473-A1 QUINOLINE DERIVATIVES CFTR, NQO1, IRF3 KDM4E 2522/4885L3MBTL1 4861/4885MPI 2348/4885

“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.