SCHEMBL19087158

SCHEMBL19087158

Cc1cnn(CCC(N)=O)c1

nearest known ligand 0.52

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.52
LMNA P02545 1/20 0.52
HTT P42858 1/20 0.52
GAA P10253 5/20 0.49
KMT2A Q03164 2/20 0.49
CYP3A4 P08684 2/20 0.46
CYP2C19 P33261 2/20 0.46
NOS1 P29475 1/20 0.46
ALDH1A1 P00352 3/20 0.45
CYP1A2 P05177 2/20 0.45
ALPI P09923 1/20 0.43
ALPG P10696 1/20 0.43
PLAA Q9Y263 1/20 0.43
MEN1 O00255 1/20 0.43
CYP2C9 P11712 1/20 0.43
PDK2 Q15119 2/20 0.41
L3MBTL1 Q9Y468 1/20 0.41
KLKB1 P03952 2/20 0.39

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
SCHEMBL22489726 0.91 HTT (0.48) SMN1; SMN2LMNAHTTGAAKMT2A
SCHEMBL6937303 0.84 LMNA (0.54) SMN1; SMN2LMNAHTTGAAKMT2A
SCHEMBL10175541 0.84 LMNA (0.54) SMN1; SMN2LMNAHTTGAAKMT2A
Hydrochloric Acid SCHEMBL28842191 0.82 LMNA (0.52) SMN1; SMN2LMNAHTTGAAKMT2A
SCHEMBL13102449 0.81 ALPI (0.53) SMN1; SMN2LMNAHTTGAAKMT2A
SCHEMBL26085647 0.81 LMNA (0.55) SMN1; SMN2LMNAHTTGAAKMT2A
SCHEMBL28603762 0.80 PDK2 (0.42) SMN1; SMN2LMNAHTTGAAKMT2A
SCHEMBL24211171 0.79 L3MBTL1 (0.42) SMN1; SMN2LMNAHTTGAAKMT2A
SCHEMBL19077854 0.79 PDK2 (0.40) SMN1; SMN2LMNAHTTGAAKMT2A
SCHEMBL21576892 0.79 LMNA (0.50) SMN1; SMN2LMNAHTTGAAKMT2A

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 7 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024015251-A1 INHIBITORS OF HPK1 AND METHODS OF USE THEREOF ARCUS BIOSCIENCES, INC. (US) 2024-01-18 WO disclosed
EP-3793565-B1 MCL-1 INHIBITORS GILEAD SCIENCES INC (US) 2022-01-05 EP disclosed
EP-3904348-A1 AMINOPYRIDINE COMPOUND, PREPARATION METHOD THEREFOR AND USE THEREOF Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. (CN) 2021-11-03 EP disclosed
EP-3792256-A1 PYRIDINE AND PYRIDIMINE COMPOUNDS AS PI3K-GAMMA INHIBITORS Incyte Corporation (US) 2021-03-17 EP disclosed
EP-3400221-B1 PYRAZOL / IMIDAZOL SUBSTITUTED PYRIDINES AS PI3K-GAMMA INHIBITORS INCYTE CORP (US) 2020-08-26 EP disclosed
WO-2020135195-A1 AMINOPYRIDINE COMPOUND, PREPARATION METHOD THEREFOR AND USE THEREOF 四川科伦博泰生物医药股份有限公司 2020-07-02 WO disclosed
US-20170190689-A1 PYRIDINE AND PYRIDIMINE COMPOUNDS AS PI3K-GAMMA INHIBITORS INCYTE CORPORATION 2017-07-06 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 (1 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-20170190689-A1 PYRIDINE AND PYRIDIMINE COMPOUNDS AS PI3K-GAMMA INHIBITORS PIK3CG, PIK3CD, PIK3CB SMN1; SMN2 1910/4885LMNA 3680/4885HTT 2012/4885

“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.