SCHEMBL8638149

SCHEMBL8638149

CONC(=O)c1ccc(Cl)cc1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.61
LMNA P02545 2/20 0.61
KDM4E B2RXH2 2/20 0.61
MAPT P10636 1/20 0.61
L3MBTL1 Q9Y468 1/20 0.61
RAB9A P51151 2/20 0.54
NPC1 O15118 1/20 0.53
POLB P06746 2/20 0.52
CYP1A2 P05177 1/20 0.52
TSHR P16473 1/20 0.52
NFKB1 P19838 1/20 0.52
MAOB P27338 1/20 0.52
PTGS2 P35354 3/20 0.51
MEN1 O00255 1/20 0.50
BLM P54132 1/20 0.50
PMP22 Q01453 1/20 0.50
KMT2A Q03164 1/20 0.50
SMN1; SMN2 Q16637 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
HTT P42858 1/20 0.50

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
SCHEMBL26687397 0.84 MMP1 (0.60) ALDH1A1LMNAKDM4EMAPTL3MBTL1
SCHEMBL27951738 0.81 MAPT (0.70) ALDH1A1KDM4EMAPTL3MBTL1RAB9A
SCHEMBL14602517 0.81 LMNA (0.55) ALDH1A1LMNAKDM4EMAPTRAB9A
SCHEMBL9402939 0.81 CA1 (0.59) ALDH1A1LMNAMAPTL3MBTL1RAB9A
SCHEMBL28647585 0.81 MAPT (0.50) ALDH1A1LMNAMAPTL3MBTL1RAB9A
SCHEMBL3645797 0.81 ALDH1A1 (0.61) ALDH1A1LMNAMAPTRAB9ANPC1
SCHEMBL13568181 0.81 CSNK2A2 (0.49) ALDH1A1LMNAKDM4EMAPTL3MBTL1
SCHEMBL28960899 0.80 HDAC1 (0.55) ALDH1A1LMNAKDM4EMAPTL3MBTL1
SCHEMBL13479797 0.80 ALDH1A1 (0.57) ALDH1A1LMNAKDM4EMAPTL3MBTL1
SCHEMBL8547880 0.79 RAB9A (0.56) LMNAKDM4EMAPTRAB9ANPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113735756-B Method for synthesizing chiral 3, 3-disubstituted isoindolinone compound by rhodium catalysis 陕西师范大学 2024-04-26 CN disclosed
CN-116574056-A Preparation method of fluoroisoquinolone compound 五邑大学 2023-08-11 CN disclosed
CN-113149868-B Method for synthesizing axichiral diene compound by trivalent rhodium catalysis 陕西师范大学 2023-05-23 CN disclosed
CN-115433222-A Preparation method and application of 2- (gem-difluoropropylene) benzamide compound 五邑大学 2022-12-06 CN disclosed
CN-113735756-A Method for synthesizing chiral 3, 3-disubstituted isoindolinone compound by rhodium catalysis 陕西师范大学 2021-12-03 CN disclosed
CN-113149868-A Method for synthesizing axial chiral allene compound by using trivalent rhodium as catalyst 陕西师范大学 2021-07-23 CN disclosed
CN-110305062-B Substituted isoquinolone compound and synthesis method and application thereof 广州医科大学 2021-01-05 CN disclosed
CN-107082761-B Phenanthridinone or benzophenanthridinone derivative and synthesis method thereof 上海大学 2020-04-03 CN disclosed
CN-102532021-B Preparation method of 2-alkoxy-3,4-disubstituted isoquinoline-1(2H)-one derivatives UNIV TIANJIN 2013-10-16 CN disclosed
CN-103288711-A Preparation method of 3-hydroxy-2-alkoxy-3-phenyl-isoindol-1(2H)-ketone derivatives UNIV TIANJIN 2013-09-11 CN disclosed
EP-1666551-B1 Ink for ink jet-recording curable through irradiation and method for preparing lithographic printing plates using the same FUJIFILM CORP (JP) 2010-02-17 EP disclosed
US-7648997-B2 Immunomodulators for inducing cytokine biosynthesis, for treatment of diseases including viral and neoplastic diseases; 1-[3-(Aminooxy)propyl]-2-propyl-1H-imidazo[4,5-c]quinolin-4-amine; N-[3-(4-Amino-2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)propoxy]cyclopropanecarboxamide COLEY PHARMACEUTICAL GROUP, INC. (US) 2010-01-19 US disclosed
US-7648997-B2 Immunomodulators for inducing cytokine biosynthesis, for treatment of diseases including viral and neoplastic diseases; 1-[3-(Aminooxy)propyl]-2-propyl-1H-imidazo[4,5-c]quinolin-4-amine; N-[3-(4-Amino-2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)propoxy]cyclopropanecarboxamide COLEY PHARMACEUTICAL GROUP, INC. (US) 2010-01-19 US disclosed
US-7635181-B2 Ink for ink jet-recording curable through irradiation with a radioactive ray and method for preparing lithographic printing plates using the same FUJIFILM CORPORATION (JP) 2009-12-22 US disclosed
US-7635181-B2 Ink for ink jet-recording curable through irradiation with a radioactive ray and method for preparing lithographic printing plates using the same FUJIFILM CORPORATION (JP) 2009-12-22 US disclosed
US-20080114019-A1 Hydroxylamine Substituted Imidazoquinolines COLEY PHARMACEUTICAL GROUP, INC. (US) 2008-05-15 US disclosed
US-20080114019-A1 Hydroxylamine Substituted Imidazoquinolines COLEY PHARMACEUTICAL GROUP, INC. (US) 2008-05-15 US disclosed
US-5733935-A EXCELLENT EFFECT FOR CONTROLLING WOOD-ROT FUNGI, PLANT DISEASES, FUNGI OF HUMANS AND ANIMALS, ALSO USEFUL AS INDUSTRIAL, AGRICULTURAL AND MEDICAL FUNGICIDE; IODOPROPARGYL DERIVATIVES NIHON NOHYAKU CO., LTD. (JP) 1998-03-31 US disclosed
EP-0751120-A2 Hydroxylamine derivatives and fungicides containing the same Nihon Nohyaku Co., Ltd. (JP) 1997-01-02 EP disclosed
US-5319123-A Reacting an N-alkoxyamide with an acyl halide in the presence of a hindered base SANDOZ LTD. (CH) 1994-06-07 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-20080114019-A1 Hydroxylamine Substituted Imidazoquinolines IFNG, IRF3, IL2 ALDH1A1 513/4885LMNA 4187/4885KDM4E 1198/4885

“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.