SCHEMBL4742798

SCHEMBL4742798

CC(C(=O)Cl)N1C(=O)c2ccccc2C1=O

nearest known ligand 0.70

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 2/20 0.64
▸ ALDH1A1 P00352 4/20 0.57
▸ HTT P42858 3/20 0.57
▸ NPC1 O15118 1/20 0.55
▸ KMT2A Q03164 2/20 0.54
▸ GAA P10253 1/20 0.54
▸ TSHR P16473 2/20 0.53
▸ POLB P06746 2/20 0.53
▸ MAPT P10636 1/20 0.53
▸ USP2 O75604 1/20 0.51
▸ HPGD P15428 1/20 0.50
▸ ALOX15 P16050 1/20 0.49
▸ MAPK1 P28482 1/20 0.49
▸ SMN1; SMN2 Q16637 1/20 0.49

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
SCHEMBL5384717 1.00 LMNA (0.64) LMNAALDH1A1HTTNPC1KMT2A
SCHEMBL29556341 1.00 LMNA (0.64) LMNAALDH1A1HTTNPC1KMT2A
SCHEMBL10354184 1.00 LMNA (0.64) LMNAALDH1A1HTTNPC1KMT2A
SCHEMBL10577708 0.84 LMNA (0.68) LMNAALDH1A1HTTNPC1KMT2A
SCHEMBL125972 0.82 LMNA (0.71) LMNAALDH1A1HTTNPC1KMT2A
SCHEMBL29472125 0.82 LMNA (0.71) LMNAALDH1A1HTTNPC1KMT2A
SCHEMBL7399848 0.82 LMNA (0.71) LMNAALDH1A1HTTNPC1KMT2A
SCHEMBL8977751 0.82 LMNA (0.66) LMNAALDH1A1HTTNPC1KMT2A
SCHEMBL478339 0.82 LMNA (0.71) LMNAALDH1A1HTTNPC1KMT2A
SCHEMBL19359219 0.81 TP53 (0.60) LMNAALDH1A1HTTNPC1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12564583-B2 Small molecules against cereblon to enhance effector T cell function Lee Moffitt Cancer Center and Research Institute, Inc. (US) 2026-03-03 — — US disclosed
US-12384769-B2 Heteroaryl-substituted aminoalkyl azole compounds as pesticides ELANCO ANIMAL HEALTH GMBH (DE) 2025-08-12 — — US disclosed
EP-3924349-B1 AMINO ACID DERIVATIVES FOR THE TREATMENT OF INFLAMMATORY DISEASES THE ROSKAMP INST (US) 2025-06-25 — — EP disclosed
CN-115996639-B Novel heteroaryl-triazole compounds as pesticides 拜耳公司 2025-06-13 — — CN disclosed
EP-2895488-B1 TRICYCLIC GYRASE INHIBITORS FOR USE AS ANTIBACTERIAL AGENTS MERCK SHARP & DOHME LLC (US) 2024-12-11 — — EP disclosed
CN-113939509-B Novel heteroaryl substituted aminoalkylazole compounds as pesticides 拜耳动物保健有限责任公司 2024-11-29 — — CN disclosed
CN-114502545-B Novel heteroaryl-triazole compounds as pesticides 拜耳公司 2024-06-28 — — CN disclosed
CN-115551839-B Heteroaryl-triazole compounds as pesticides 拜耳公司 2024-06-04 — — CN disclosed
US-20230348432-A1 NOVEL HETEROARYL-TRIAZOLE COMPOUNDS AS PESTICIDES BAYER AKTIENGESELLSCHAFT (DE) 2023-11-02 — — US disclosed
US-20230348432-A1 NOVEL HETEROARYL-TRIAZOLE COMPOUNDS AS PESTICIDES BAYER AKTIENGESELLSCHAFT (DE) 2023-11-02 — — US disclosed
WO-1996013485-A1 PYRIDOPYRIMIDONES, QUINOLINES AND FUSED N-HERETOCYCLES AS BRADYKININ ANTAGONISTS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1996-05-09 — — WO disclosed
EP-0198325-B1 SUBSTITUTED ANILINE DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 1992-07-15 — — EP disclosed
EP-0197478-B1 DIPHOSPHONIC-ACID DERIVATIVES, PROCESS FOR PREPARING THEM AND MEDICINES CONTAINING THESE COMPOUNDS Roche Diagnostics GmbH (DE) 1990-09-19 — — EP disclosed
US-4891429-A CHEMICAL INTERMEDIATES HOFFMANN-LA ROCHE INC. (US) 1990-01-02 — — US disclosed
US-4849436-A TREATMENT OF CARDIOVASCULAR DISORDERS NELSON RESEARCH & DEVELOPMENT CO. (US) 1989-07-18 — — US disclosed
EP-0259462-A1 1,4-DIHYDROPYRIDINES Whitby Research Incorporated (US) 1988-03-16 — — EP disclosed
US-4696930-A CARDIOVASCULAR DISORDERS, ANTICOAGULANTS HOFFMANN-LA ROCHE INC. (US) 1987-09-29 — — US disclosed
WO-1987005512-A1 1,4-DIHYDROPYRIDINES NELSON RESEARCH AND DEVELOPMENT COMPANY (US) 1987-09-24 — — WO disclosed
EP-0198325-A2 Substituted aniline derivatives F. HOFFMANN-LA ROCHE AG (CH) 1986-10-22 — — EP disclosed
EP-0197478-A1 Diphosphonic-acid derivatives, process for preparing them and medicines containing these compounds Roche Diagnostics GmbH (DE) 1986-10-15 — — 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 (3 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-20230348432-A1 NOVEL HETEROARYL-TRIAZOLE COMPOUNDS AS PESTICIDES CYP4F3, CYP4X1, GLRX3 LMNA 3318/4885ALDH1A1 3747/4885HTT 1738/4885
US-12384769-B2 Heteroaryl-substituted aminoalkyl azole compounds as pesticides DDT, CRY1, AAAS LMNA 3046/4885ALDH1A1 3552/4885HTT 1081/4885
US-12564583-B2 Small molecules against cereblon to enhance effector T cell function CRBN, CD4, ICOS LMNA 2916/4885ALDH1A1 2373/4885HTT 2677/4885

“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.

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