SCHEMBL2032093

SCHEMBL2032093

O=C(O)c1c(Cl)ncnc1Cl

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.43
ALDH1A1 P00352 2/20 0.43
MAPK1 P28482 1/20 0.43
LMNA P02545 1/20 0.40
DPP4 P27487 1/20 0.39
KMO O15229 7/20 0.38
NAPRT Q6XQN6 1/20 0.37
KDM4E B2RXH2 1/20 0.34
HSD17B10 Q99714 1/20 0.34
KEAP1 Q14145 1/20 0.34
NFE2L2 Q16236 1/20 0.34
EGLN1 Q9GZT9 1/20 0.34
ALOX15 P16050 1/20 0.33
TSHR P16473 1/20 0.33
CA12 O43570 1/20 0.33
CA1 P00915 1/20 0.33
CA2 P00918 1/20 0.33
CA7 P43166 1/20 0.33
CA9 Q16790 1/20 0.33
CA14 Q9ULX7 1/20 0.33

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
Hydrochloric Acid SCHEMBL17713984 0.97 SMN1; SMN2 (0.42) SMN1; SMN2ALDH1A1MAPK1LMNADPP4
Formaldehyde SCHEMBL27853879 0.95 SMN1; SMN2 (0.41) SMN1; SMN2ALDH1A1MAPK1LMNADPP4
SCHEMBL16984947 0.84 ALDH1A1 (0.46) SMN1; SMN2ALDH1A1MAPK1LMNADPP4
SCHEMBL15649175 0.84 EGFR (0.39) SMN1; SMN2ALDH1A1MAPK1LMNADPP4
SCHEMBL15524835 0.81 PDE4A (0.34) SMN1; SMN2ALDH1A1MAPK1LMNAKMO
SCHEMBL15170169 0.80 SMN1; SMN2 (0.34) SMN1; SMN2ALDH1A1MAPK1LMNADPP4
SCHEMBL18113766 0.80 ALDH1A1 (0.42) SMN1; SMN2ALDH1A1MAPK1LMNAKMO
SCHEMBL15170666 0.80 ALDH1A1 (0.38) SMN1; SMN2ALDH1A1MAPK1LMNAKMO
SCHEMBL374759 0.79 ALDH1A1 (0.42) SMN1; SMN2ALDH1A1MAPK1LMNAKMO
Hydrochloric Acid SCHEMBL10558900 0.78 ALDH1A1 (0.41) SMN1; SMN2ALDH1A1MAPK1LMNAKMO

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116514782-B Synthesis method of baratinib related substances 江苏海悦康医药科技有限公司 2025-05-13 CN claimed
CN-116514782-A Synthesis method of baratinib related substances 江苏海悦康医药科技有限公司 2023-08-01 CN claimed
CN-110981816-B Synthesis method of 4-amino-2, 6-dimethoxypyrimidine 天和药业股份有限公司 2022-07-05 CN claimed
CN-110981816-A Synthesis method of 4-amino-2, 6-dimethoxypyrimidine 扬州天和药业有限公司 2020-04-10 CN claimed
CN-110028502-B Preparation method of kinase inhibitor drug intermediate 济南周行医药科技有限公司 2020-02-14 CN claimed
CN-110028502-A A kind of preparation method of kinase inhibitors drug intermediate 济南周行医药科技有限公司 2019-07-19 CN claimed
WO-2026107328-A1 AGONISTS OF PARATHYROID HORMONE 1 AND INCRETIN RECEPTORS SEPTERNA, INC. (US) 2026-05-21 WO disclosed
CN-116514782-B Synthesis method of baratinib related substances 江苏海悦康医药科技有限公司 2025-05-13 CN disclosed
CN-116514782-B Synthesis method of baratinib related substances 江苏海悦康医药科技有限公司 2025-05-13 CN disclosed
US-20250129044-A1 PYRIDINYL DERIVATIVES AS SODIUM CHANNEL ACTIVATORS XENON PHARMACEUTICALS INC. (CA) 2025-04-24 US disclosed
US-20250099442-A1 COMPOUNDS FOR USE IN TREATING NEUROLOGICAL DISORDERS PROTHENA BIOSCIENCES INC 2025-03-27 US disclosed
EP-4281454-B1 PROCESS FOR MAKING IBRUTINIB SYNTHON BV (NL) 2025-03-05 EP disclosed
EP-4444721-A1 COMPOUNDS FOR USE IN TREATING NEUROLOGICAL DISORDERS Prothena Biosciences Limited (IE) 2024-10-16 EP disclosed
WO-2014054053-A1 SPIROCYCLIC COMPOUNDS, COMPOSITIONS AND MEDICINAL APPLICATIONS THEREOF ADVINUS THERAPEUTICS LIMITED (IN) 2014-04-10 WO disclosed
US-20130231306-A1 AMINO PYRIMIDINE ANTICANCER COMPOUNDS OSI Pharmaceuticals, LLC (US) 2013-09-05 US disclosed
US-8399433-B2 Amino pyrimidine anticancer compounds OSI Pharmaceuticals, LLC (US) 2013-03-19 US disclosed
CN-102448955-A Aminopyrimidine Anticancer Compounds OSI PHARM INC 2012-05-09 CN disclosed
EP-2438056-A2 AMINO PYRIMIDINE ANTICANCER COMPOUNDS OSI Pharmaceuticals, LLC (US) 2012-04-11 EP disclosed
US-20110136764-A1 AMINO PYRIMIDINE ANTICANCER COMPOUNDS OSI PHARMACEUTICALS, INC. (US) 2011-06-09 US disclosed
WO-2010141406-A2 AMINO PYRIMIDINE ANTICANCER COMPOUNDS OSI PHARMACEUTICALS, INC. (US) 2010-12-09 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 (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-20250129044-A1 PYRIDINYL DERIVATIVES AS SODIUM CHANNEL ACTIVATORS SCN1B, SCN1A, SCN2B SMN1; SMN2 564/4885ALDH1A1 1828/4885MAPK1 1372/4885
US-20130231306-A1 AMINO PYRIMIDINE ANTICANCER COMPOUNDS DPYD, PTK2, TYMS SMN1; SMN2 1215/4885ALDH1A1 1117/4885MAPK1 290/4885
US-20250099442-A1 COMPOUNDS FOR USE IN TREATING NEUROLOGICAL DISORDERS DYRK2, DYRK1A, DYRK1B SMN1; SMN2 65/4885ALDH1A1 2359/4885MAPK1 243/4885
US-20110136764-A1 AMINO PYRIMIDINE ANTICANCER COMPOUNDS DPYD, PTK2, TYMS SMN1; SMN2 1215/4885ALDH1A1 1117/4885MAPK1 290/4885

“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.