SCHEMBL48577

SCHEMBL48577

O=Cc1ccc(Cl)c(Cl)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 1.00
VCAM1 P19320 1/20 0.55
ALDH1A3 P47895 3/20 0.53
HSD17B10 Q99714 1/20 0.52
ALDH3A1 P30838 2/20 0.48
KDM4E B2RXH2 1/20 0.46
PTGS2 P35354 1/20 0.46
RAB9A P51151 1/20 0.46
PYGL P06737 3/20 0.44
IGF1R P08069 1/20 0.44
NPFFR2 Q9Y5X5 2/20 0.44
KMT2A Q03164 1/20 0.44
NPSR1 Q6W5P4 1/20 0.44
CHAT P28329 1/20 0.44
AHR P35869 1/20 0.43
TP53 P04637 1/20 0.43
CYP2A6 P11509 1/20 0.43
KDM4A O75164 1/20 0.43
KDM4B O94953 1/20 0.43
TTR P02766 1/20 0.42

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
SCHEMBL29364412 1.00 ALDH1A1 (1.00) ALDH1A1VCAM1ALDH1A3HSD17B10ALDH3A1
Hydrochloric Acid SCHEMBL28849470 0.97 ALDH1A1 (0.95) ALDH1A1VCAM1ALDH1A3HSD17B10ALDH3A1
Hydrochloric Acid SCHEMBL28849465 0.95 ALDH1A1 (0.91) ALDH1A1VCAM1ALDH1A3HSD17B10ALDH3A1
Methylene Chloride SCHEMBL27781502 0.93 ALDH1A1 (0.86) ALDH1A1VCAM1ALDH1A3HSD17B10ALDH3A1
SCHEMBL29080593 0.91 ALDH1A1 (0.83) ALDH1A1VCAM1ALDH1A3HSD17B10ALDH3A1
Glycine SCHEMBL8216583 0.82 ALDH1A1 (0.68) ALDH1A1VCAM1ALDH1A3ALDH3A1PYGL
SCHEMBL4372478 0.81 ALDH1A1 (0.68) ALDH1A1VCAM1HSD17B10KDM4EKMT2A
SCHEMBL29818700 0.80 ALDH1A1 (0.67) ALDH1A1VCAM1ALDH1A3HSD17B10ALDH3A1
SCHEMBL30493606 0.80 ALDH1A1 (0.67) ALDH1A1VCAM1ALDH1A3HSD17B10ALDH3A1
SCHEMBL3787764 0.80 ALDH1A1 (0.67) ALDH1A1VCAM1ALDH1A3HSD17B10ALDH3A1

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

Appears in 3384 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117624148-A Polyhydroxy sulfonium salt derivative with disubstituted benzene ring, preparation method and medical application thereof 中国药科大学 2024-03-01 CN claimed
CN-117510350-A Stilbene And-1 protein degradation agent, preparation method And application thereof 中国医学科学院放射医学研究所 2024-02-06 CN claimed
CN-117247359-A Dendrimer-like lipid compound, liposome, lipid complex, lipid nanoparticle and application thereof 中国科学院广州生物医药与健康研究院 2023-12-19 CN claimed
WO-2023236824-A1 DENDRON-LIKE LIPID COMPOUND, LIPOSOME, LIPID COMPLEX, AND LIPID NANOPARTICLE AND USE THEREOF 中国科学院广州生物医药与健康研究院 2023-12-14 WO claimed
CN-117004219-A Preparation method of composite anion exchange membrane 北京未来氢能科技有限公司 2023-11-07 CN claimed
CN-109651291-B Polysubstituted naphtho [1,2-d ] thiazole and derivative and synthesis method thereof 广东蓝天优创美化妆品有限公司 2023-07-07 CN claimed
CN-116143689-A Synthesis method of 2,3,5, 6-tetra-substituted pyridine compound 重庆医科大学 2023-05-23 CN claimed
CN-115572289-A Synthesis method of tesofensine 龙曦宁(上海)医药科技有限公司 2023-01-06 CN claimed
CN-115215863-A Preparation method of pharmaceutical intermediate 6,9-dihydro-1H-pyrazolo [3,4-f ] quinoline-8-nitrile derivative 南京欣久医药科技有限公司 2022-10-21 CN claimed
CN-114891011-A Preparation method of medical intermediate 2-amino-tetrahydropyrano [3, 2-c ] quinoline-5-ketone derivative 南京苏亦欣医药科技有限公司 2022-08-12 CN claimed
US-4868241-A POLYVINYL ALCOHOL MODIFIED WITH BENZOIC ACID DERIVATIVE AMERICAN CYANAMID COMPANY (US) 1989-09-19 US claimed
WO-1988005774-A1 DERIVATIVES OF (R) 5-PENTYLAMINO-5-OXOPENTANOIC ACID WITH ANTICHOLECYSTOKININ ACTIVITY ROTTA RESEARCH LABORATORIUM S.P.A. (IT) 1988-08-11 WO claimed
EP-0231922-A2 Electron beam and X-ray resists AMERICAN CYANAMID COMPANY (US) 1987-08-12 EP claimed
EP-0057844-B1 PROCESS FOR THE PREPARATION OF POLYCHLOROBENZOYL CHLORIDES BAYER AG (DE) 1983-12-28 EP claimed
US-4380629-A Styryl-like compounds showing a color-developing and bleaching behavior with improved stability and prolonged lifetime MATSUSHITA ELECTRIC INDUSTRIAL COMPANY, LIMITED (JP) 1983-04-19 US claimed
EP-0000092-B1 METHOD OF PREPARING ASCORBIC ACID AND INTERMEDIATES SPECIALLY ADAPTED FOR USE THEREIN PFIZER INC. (US) 1981-04-29 EP claimed
US-4147862-A Method of preparing styryl-like compounds MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) 1979-04-03 US claimed
EP-0000092-A1 Method of preparing ascorbic acid and intermediates specially adapted for use therein PFIZER INC. (US) 1978-12-20 EP claimed
US-4111958-A Ascorbic acid synthesis PFIZER INC. (US) 1978-09-05 US claimed
US-3965107-A Isothiazolopyridinones ROHM AND HAAS COMPANY (US) 1976-06-22 US claimed