SCHEMBL266386

SCHEMBL266386

CC(C)NC(=O)c1cccc(Br)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.69
CYP1A2 P05177 3/20 0.62
CYP2C19 P33261 3/20 0.62
CYP3A4 P08684 2/20 0.62
CYP2C9 P11712 1/20 0.62
NPSR1 Q6W5P4 1/20 0.59
SMN1; SMN2 Q16637 5/20 0.59
NPC1 O15118 2/20 0.59
RAB9A P51151 2/20 0.59
CASP3 P42574 1/20 0.59
SENP8 Q96LD8 1/20 0.59
SENP7 Q9BQF6 1/20 0.59
SENP6 Q9GZR1 1/20 0.59
L3MBTL1 Q9Y468 2/20 0.58
MEN1 O00255 2/20 0.54
KMT2A Q03164 2/20 0.54
HTT P42858 1/20 0.54
PARP1 P09874 1/20 0.52
CHRNA1 P02708 1/20 0.51
CHRNG P07510 1/20 0.51

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
SCHEMBL8593124 0.87 NPSR1 (0.69) ALDH1A1CYP3A4NPSR1SMN1; SMN2KMT2A
SCHEMBL27611123 0.85 ALDH1A1 (0.68) ALDH1A1CYP1A2CYP2C19CYP3A4CYP2C9
SCHEMBL13753669 0.83 HPGD (0.71) ALDH1A1CYP1A2CYP2C19CYP3A4CYP2C9
SCHEMBL15486211 0.83 SMN1; SMN2 (0.59) ALDH1A1CYP1A2CYP2C19SMN1; SMN2NPC1
SCHEMBL29818016 0.83 ALDH1A1 (0.61) ALDH1A1CYP1A2CYP2C19CYP3A4CYP2C9
SCHEMBL13753288 0.82 ALDH1A1 (0.61) ALDH1A1CYP1A2CYP2C19CYP3A4CYP2C9
SCHEMBL13753287 0.82 ALDH1A1 (0.61) ALDH1A1CYP1A2CYP2C19CYP3A4CYP2C9
SCHEMBL20717755 0.82 ALDH1A1 (0.65) ALDH1A1CYP1A2CYP2C19CYP3A4CYP2C9
SCHEMBL8547159 0.82 ALDH1A1 (1.00) ALDH1A1CYP1A2CYP2C19CYP3A4CYP2C9
SCHEMBL13761476 0.81 ALDH1A1 (0.59) ALDH1A1CYP1A2CYP2C19CYP3A4CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260070902-A1 SULFONYL DERIVATIVES AS CCR6 INHIBITORS HOFFMANN-LA ROCHE INC. (US) 2026-03-12 US disclosed
EP-4630402-A1 SULFONYL DERIVATIVES AS CCR6 INHIBITORS F. Hoffmann-La Roche AG (CH) 2025-10-15 EP disclosed
US-12247018-B2 Aryl-n-aryl derivatives for treating a RNA virus infection ABIVAX (FR) 2025-03-11 US disclosed
CN-118480001-A C-Kit (V559D)/PDGFR beta double-target allosteric inhibitor and preparation method, pharmaceutical composition and application thereof 贵州省天然产物研究中心 2024-08-13 CN disclosed
WO-2024121013-A1 SULFONYL DERIVATIVES AS CCR6 INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2024-06-13 WO disclosed
CN-112638876-B phenyl/pyridinyl-N-phenyl/pyridinyl derivatives for the treatment of RNA viral infections ABIVAX公司 2023-12-26 CN disclosed
EP-3820849-B1 PHENYL/PYRIDYL-NH-PHENYL/PYRIDYL DERIVATIVES FOR TREATING RNA VIRUS INFECTION ABIVAX (FR) 2023-09-06 EP disclosed
US-20220356175-A1 ARYL-N-ARYL DERIVATIVES FOR TREATING A RNA VIRUS INFECTION ABIVAX (FR) 2022-11-10 US disclosed
US-20210283265-A1 METHODS AND COMPOUNDS FOR THE TREATMENT OF GENETIC DISEASE Design Therapeutics, Inc. 2021-09-16 US disclosed
EP-3820849-A1 PHENYL/PYRIDYL-N-PHENYL/PYRIDYL DERIVATIVES FOR TREATING RNA VIRUS INFECTION ABIVAX (FR) 2021-05-19 EP disclosed
US-20070259904-A1 Bi-aryl meta-pyrimidine inhibitors of kinases TARGEGEN, INC. (US) 2007-11-08 US disclosed
US-20070259904-A1 Bi-aryl meta-pyrimidine inhibitors of kinases TARGEGEN, INC. (US) 2007-11-08 US disclosed
US-20070259904-A1 Bi-aryl meta-pyrimidine inhibitors of kinases TARGEGEN, INC. (US) 2007-11-08 US disclosed
US-20070191405-A1 Bi-aryl meta-pyrimidine inhibitors of kinases TARGEGEN, INC. (US) 2007-08-16 US disclosed
US-20070191405-A1 Bi-aryl meta-pyrimidine inhibitors of kinases TARGEGEN, INC. (US) 2007-08-16 US disclosed
US-20070191405-A1 Bi-aryl meta-pyrimidine inhibitors of kinases TARGEGEN, INC. (US) 2007-08-16 US disclosed
WO-2007053452-A1 BI-ARYL META-PYRIMIDINE INHIBITORS OF KINASES TARGEGEN, INC. (US) 2007-05-10 WO disclosed
EP-1227086-B1 1-SUBSTITUTED PHENYL-1-(1H-IMIDAZOL-4-YL) ALCOHOLS, PROCESS FOR PRODUCING THE SAME AND USE THEREOF TAKEDA PHARMACEUTICAL (JP) 2006-03-29 EP disclosed
US-6518257-B1 1-substituted phenyl-1-(1h-imidazol-4-yl) alcohols, process for producing the same and use thereof TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2003-02-11 US disclosed
EP-1227086-A1 1-SUBSTITUTED PHENYL-1-(1H-IMIDAZOL-4-YL) ALCOHOLS, PROCESS FOR PRODUCING THE SAME AND USE THEREOF Takeda Chemical Industries, Ltd. (JP) 2002-07-31 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 (6 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-20070191405-A1 Bi-aryl meta-pyrimidine inhibitors of kinases JAK2, TYK2, JAK3 ALDH1A1 3235/4885CYP1A2 1622/4885CYP2C19 1461/4885
US-20220356175-A1 ARYL-N-ARYL DERIVATIVES FOR TREATING A RNA VIRUS INFECTION CRKL, VRK2, FRK ALDH1A1 4186/4885CYP1A2 1900/4885CYP2C19 2361/4885
US-20260070902-A1 SULFONYL DERIVATIVES AS CCR6 INHIBITORS CCR6, CCR1, CCR4 ALDH1A1 2086/4885CYP1A2 2296/4885CYP2C19 2388/4885
US-20210283265-A1 METHODS AND COMPOUNDS FOR THE TREATMENT OF GENETIC DISEASE NEDD4, CBL, UBQLN2 ALDH1A1 4642/4885CYP1A2 4867/4885CYP2C19 4884/4885
US-20070259904-A1 Bi-aryl meta-pyrimidine inhibitors of kinases JAK2, TYK2, JAK3 ALDH1A1 3235/4885CYP1A2 1622/4885CYP2C19 1461/4885
US-12247018-B2 Aryl-n-aryl derivatives for treating a RNA virus infection CRKL, VRK2, FRK ALDH1A1 4163/4885CYP1A2 1897/4885CYP2C19 2391/4885

“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.