SCHEMBL1663526

SCHEMBL1663526

CNC(=O)c1ccc[nH]c1=O

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NAPRT Q6XQN6 1/20 0.60
TYK2 P29597 1/20 0.54
RAB9A P51151 2/20 0.52
NPC1 O15118 1/20 0.52
GAA P10253 3/20 0.48
SMYD3 Q9H7B4 2/20 0.48
PLK1 P53350 1/20 0.46
DAO P14920 1/20 0.45
KDM4E B2RXH2 3/20 0.41
MAPT P10636 2/20 0.41
MEN1 O00255 1/20 0.41
POLB P06746 1/20 0.41
THRB P10828 1/20 0.41
BLM P54132 1/20 0.41
KMT2A Q03164 1/20 0.41
L3MBTL1 Q9Y468 1/20 0.41
AURKA O14965 1/20 0.41
AURKB Q96GD4 1/20 0.41
INCENP Q9NQS7 1/20 0.41
MAPK1 P28482 1/20 0.40

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
SCHEMBL2352415 0.84 KDM4E (0.48) NAPRTTYK2RAB9ANPC1GAA
SCHEMBL6916843 0.82 NAPRT (0.62) NAPRTTYK2RAB9ANPC1GAA
SCHEMBL109595 0.81 NAPRT (0.60) NAPRTTYK2RAB9ANPC1GAA
SCHEMBL9936595 0.79 GAA (0.61) NAPRTGAAPLK1KDM4EMAPT
SCHEMBL3182033 0.78 NAPRT (0.67) NAPRTTYK2RAB9ANPC1GAA
SCHEMBL16982383 0.78 NAPRT (0.51) NAPRTTYK2RAB9ANPC1GAA
SCHEMBL425117 0.77 NAPRT (0.72) NAPRTTYK2RAB9ANPC1GAA
SCHEMBL8193694 0.77 NAPRT (0.72) NAPRTTYK2RAB9ANPC1GAA
SCHEMBL680683 0.77 NAPRT (0.60) NAPRTTYK2GAAKDM4EMAPT
SCHEMBL3368022 0.77 TYK2 (0.70) NAPRTTYK2RAB9ANPC1GAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1861371-A1 NOVEL COMPOUNDS II 2-PYRIDINE DERIVATIVES AS INHIBITORS OF NEUTROPHILE ELASTASE. AstraZeneca AB (SE) 2007-12-05 EP claimed
WO-2006098684-A1 NOVEL COMPOUNDS II 2-PYRIDINE DERIVATIVES AS INHIBITORS OF NEUTROPHILE ELASTASE. ASTRAZENECA AB (SE) 2006-09-21 WO claimed
CN-115697993-B Pyrimidine compounds as AXL inhibitors 南京正大天晴制药有限公司 2024-12-10 CN disclosed
CN-115697993-A Pyrimidines as AXL inhibitors 南京正大天晴制药有限公司 2023-02-03 CN disclosed
US-20220356185-A1 MERTK DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS, INC. 2022-11-10 US disclosed
WO-2021011871-A1 MERTK DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS, INC. (US) 2021-01-21 WO disclosed
US-10442810-B2 Pyrrolotriazine compounds as TAM inhibitors INCYTE CORPORATION (US) 2019-10-15 US disclosed
CN-108290866-A 2- oxo -1,2- dihydropyridine -3,5- diformamide compounds as bromine structural domain inhibitor 葛兰素史克知识产权第二有限公司 2018-07-17 CN disclosed
EP-3334458-A1 COMBINATION THERAPY FOR CANCER Imclone, LLC (US) 2018-06-20 EP disclosed
CN-108137542-A Pyridone diformamide as bromine structural domain inhibitor 葛兰素史克知识产权第二有限公司 2018-06-08 CN disclosed
US-9981975-B2 Pyrrolotriazine compounds as tam inhibitors INCYTE CORPORATION (US) 2018-05-29 US disclosed
US-7704998-B2 anticancer agents; catalytic hydrogenation JANSSEN PHARMACEUTICA N.V. (BE) 2010-04-27 US disclosed
EP-1485365-B1 SULFONYL-DERIVATIVES AS NOVEL INHIBITORS OF HISTONE DEACETYLASE JANSSEN PHARMACEUTICA NV (BE) 2008-05-14 EP disclosed
US-20080108601-A1 anticancer agents; catalytic hydrogenation VAN EMELEN KRISTOF 2008-05-08 US disclosed
US-20080108601-A1 anticancer agents; catalytic hydrogenation VAN EMELEN KRISTOF 2008-05-08 US disclosed
US-20070142393-A1 SULFONYL-DERIVATIVES AS NOVEL INHIBITORS OF HISTONE DEACETYLASE EMELEN KRISTOF V 2007-06-21 US disclosed
US-20070142393-A1 SULFONYL-DERIVATIVES AS NOVEL INHIBITORS OF HISTONE DEACETYLASE EMELEN KRISTOF V 2007-06-21 US disclosed
US-7205304-B2 medicine to inhibit proliferative conditions, such as cancer and psoriasis JANSSEN PHARMACEUTICA N.V. (BE) 2007-04-17 US disclosed
US-7205304-B2 medicine to inhibit proliferative conditions, such as cancer and psoriasis JANSSEN PHARMACEUTICA N.V. (BE) 2007-04-17 US disclosed
EP-0204335-A2 2(1H)-Pyridin-ones useful as intermediates STERLING DRUG INC. (US) 1986-12-10 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-10442810-B2 Pyrrolotriazine compounds as TAM inhibitors MERTK, MAP3K15, MAP3K5 NAPRT 704/4885TYK2 213/4885RAB9A 2040/4885
US-20220356185-A1 MERTK DEGRADERS AND USES THEREOF MERTK, ITK, CRKL NAPRT 331/4885TYK2 219/4885RAB9A 4545/4885
US-20070142393-A1 SULFONYL-DERIVATIVES AS NOVEL INHIBITORS OF HISTONE DEACETYLASE HDAC3, HDAC1, HDAC11 NAPRT 1027/4885TYK2 2903/4885RAB9A 2186/4885
US-20080108601-A1 anticancer agents; catalytic hydrogenation HDAC1, HDAC11, HDAC3 NAPRT 1868/4885TYK2 3203/4885RAB9A 1351/4885

“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.