SCHEMBL427326

SCHEMBL427326

CC(=O)c1cccnc1Cl

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.68
SMN1; SMN2 Q16637 1/20 0.68
HTT P42858 1/20 0.54
ALDH1A1 P00352 2/20 0.51
POLB P06746 2/20 0.50
EGFR P00533 2/20 0.49
NPC1 O15118 1/20 0.49
L3MBTL1 Q9Y468 1/20 0.49
MEN1 O00255 1/20 0.48
KMT2A Q03164 1/20 0.48
CYP1A2 P05177 1/20 0.47
CYP2C9 P11712 1/20 0.47
CYP2C19 P33261 1/20 0.47
CASP3 P42574 1/20 0.47
SENP8 Q96LD8 1/20 0.47
SENP7 Q9BQF6 1/20 0.47
SENP6 Q9GZR1 1/20 0.47
GFER P55789 1/20 0.46
MAPT P10636 1/20 0.46
RAB9A P51151 1/20 0.46

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
SCHEMBL29894130 1.00 LMNA (0.68) LMNASMN1; SMN2HTTALDH1A1POLB
SCHEMBL950218 0.83 LMNA (0.73) LMNASMN1; SMN2ALDH1A1POLBEGFR
Ethane SCHEMBL3957942 0.82 SMN1; SMN2 (0.92) LMNASMN1; SMN2ALDH1A1POLBEGFR
SCHEMBL29799007 0.81 SMN1; SMN2 (0.70) LMNASMN1; SMN2ALDH1A1POLBEGFR
SCHEMBL29412848 0.81 SMN1; SMN2 (1.00) LMNASMN1; SMN2ALDH1A1POLBEGFR
SCHEMBL353141 0.81 SMN1; SMN2 (1.00) LMNASMN1; SMN2ALDH1A1POLBEGFR
SCHEMBL30792459 0.81 SMN1; SMN2 (1.00) LMNASMN1; SMN2ALDH1A1POLBEGFR
SCHEMBL17180592 0.81 LMNA (0.70) LMNASMN1; SMN2HTTALDH1A1POLB
SCHEMBL105459 0.81 SMN1; SMN2 (0.70) LMNASMN1; SMN2ALDH1A1POLBEGFR
SCHEMBL15197116 0.79 LMNA (0.49) LMNASMN1; SMN2HTTALDH1A1POLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115611802-B Synthetic method of 3-acetyl-2-chloropyridine 北京迪泰医药科技有限公司 2023-03-14 CN claimed
CN-115611802-A Synthetic method of 3-acetyl-2-chloropyridine 北京迪泰医药科技有限公司 2023-01-17 CN claimed
CN-110117246-A A kind of preparation method of 3- indoles pimelie kelone compounds 山西大学 2019-08-13 CN claimed
US-20260125364-A1 HETEROAROMATIC COMPOUNDS AND THEIR USE AS DOPAMINE D1 LIGANDS PFIZER (US) 2026-05-07 US disclosed
US-20260115174-A1 PHARMACOLOGICAL CORRECTORS OF RHODOPSIN AND USES THEREOF OCTANT INC (US) 2026-04-30 US disclosed
US-20260034126-A1 KRAS INHIBITORS INCYTE CORP (US) 2026-02-05 US disclosed
WO-2025245127-A1 SPIROCYCLIC DIHYDROPYRANOPYRIMIDINE KRAS INHIBITORS Treeline Biosciences, Inc. (US) 2025-11-27 WO disclosed
EP-4649077-A1 SPIRO DERIVATIVES AS M4 ACTIVATORS/MODULATORS AND USES THEREOF Cerevel Therapeutics, LLC (US) 2025-11-19 EP disclosed
US-12454547-B2 Steroidal compositions and methods of treating lipogenic cancers Asteroid Therapeutics (US) 2025-10-28 US disclosed
EP-4587014-A2 C5AR1 ANTAGONISTS AND USES THEREOF Vanqua Bio, Inc. (US) 2025-07-23 EP disclosed
US-20250195445-A1 LONG-LASTING ANTIMICROBIAL COMPOSITIONS CONTAINING CATIONIC ACTIVE AGENTS AND ANIONIC EXCIPIENTS AND USES UNIVERSIDADE FEDERAL DE MINAS GERAIS - UFMG (BR) 2025-06-19 US disclosed
US-5541215-A ANTIRETROVIRAL COMPOUNDS; TREATING HIV INFECTIONS JANSSEN PHARMACEUTICA N.V. (BE) 1996-07-30 US disclosed
EP-0711757-A1 3-(4-phenylpiperazin-1-yl)propyl-amino, thio and oxy -pyridine, pyrimidine and benzene derivatives as alpha1-adrenoceptor antagonists F. Hoffmann-La Roche AG (CH) 1996-05-15 EP disclosed
US-5480997-A VIRICIDE FOR HIV JANSSEN PHARMACEUTICA N.V. (BE) 1996-01-02 US disclosed
EP-0672042-A1 PHARMACOLOGICALLY ACTIVE PYRIMIDINEAMINE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF Novartis AG (CH) 1995-09-20 EP disclosed
WO-1995009851-A1 PHARMACOLOGICALLY ACTIVE PYRIMIDINEAMINE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF CIBA-GEIGY AG (CH) 1995-04-13 WO disclosed
EP-0620811-A1 HETEROCYCLE-SUBSTITUTED BENZYLAMINE DERIVATIVES AS ANTIRETROVIRAL COMPOUNDS JANSSEN PHARMACEUTICA N.V. (BE) 1994-10-26 EP disclosed
WO-1993013069-A1 HETEROCYCLE-SUBSTITUTED BENZYLAMINE DERIVATIVES AS ANTIRETROVIRAL COMPOUNDS JANSSEN PHARMACEUTICA N.V. (BE) 1993-07-08 WO disclosed
US-4125618-A Novel substituted pyridines, their preparation and pharmaceutical use MERCK & CO., INC. (US) 1978-11-14 US disclosed
US-4060601-A Certain lower-alkyl amino-2'-hydroxy-propoxy pyridines MERCK & CO., INC. (US) 1977-11-29 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 (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-12454547-B2 Steroidal compositions and methods of treating lipogenic cancers SREBF1, SREBF2, NR1H3 LMNA 412/4885SMN1; SMN2 4785/4885HTT 4516/4885
US-20260125364-A1 HETEROAROMATIC COMPOUNDS AND THEIR USE AS DOPAMINE D1 LIGANDS HTR6, HTR3C, OPRD1 LMNA 2257/4885SMN1; SMN2 614/4885HTT 96/4885
US-20260115174-A1 PHARMACOLOGICAL CORRECTORS OF RHODOPSIN AND USES THEREOF PDE6D, PDE6H, ADRA1D LMNA 3152/4885SMN1; SMN2 1018/4885HTT 869/4885
US-20260034126-A1 KRAS INHIBITORS KRAS, NRAS, HRAS LMNA 4176/4885SMN1; SMN2 3185/4885HTT 3955/4885

“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.