SCHEMBL4130388

SCHEMBL4130388

Fc1cccc2nc[nH]c12

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PARP1 P09874 7/20 0.56
SMN1; SMN2 Q16637 3/20 0.39
CA12 O43570 2/20 0.39
CA9 Q16790 2/20 0.39
PDPK1 O15530 1/20 0.39
ALOX15 P16050 1/20 0.39
TNKS2 Q9H2K2 1/20 0.39
GPR84 Q9NQS5 1/20 0.37
MAPT P10636 1/20 0.37
KDM4E B2RXH2 2/20 0.35
ALDH1A1 P00352 1/20 0.35
GLA P06280 1/20 0.35
GAA P10253 1/20 0.35
HPGD P15428 1/20 0.35
HSD17B10 Q99714 1/20 0.35
MPO P05164 1/20 0.34
SLC6A4 P31645 1/20 0.34
CDK5 Q00535 1/20 0.34
CDK5R1 Q15078 1/20 0.34
CTNNB1 P35222 1/20 0.34

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
SCHEMBL196912 0.77 PARP1 (0.42) PARP1SMN1; SMN2CA12CA9PDPK1
SCHEMBL3232202 0.76 PARP1 (0.41) PARP1SMN1; SMN2CA12CA9PDPK1
SCHEMBL1445123 0.74 PDPK1 (0.41) PARP1SMN1; SMN2CA12CA9PDPK1
SCHEMBL1193119 0.74 PARP1 (0.39) PARP1MAPTKDM4EALDH1A1IP6K1
SCHEMBL29804759 0.74 PARP1 (0.39) PARP1MAPTKDM4EALDH1A1IP6K1
SCHEMBL196737 0.74 PARP1 (0.56) PARP1SMN1; SMN2CA12CA9PDPK1
SCHEMBL312428 0.74 PARP1 (0.43) PARP1SMN1; SMN2CA12CA9PDPK1
SCHEMBL30036694 0.74 PARP1 (0.43) PARP1SMN1; SMN2CA12CA9PDPK1
SCHEMBL1019602 0.74 QPCT (0.42) PARP1SMN1; SMN2CA12CA9PDPK1
SCHEMBL8668 0.74 PARP1 (0.56) PARP1SMN1; SMN2CA12CA9PDPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4200292-B1 1H-BENZO[D]IMIDAZOLE DERIVATIVES AS TLR9 INHIBITORS FOR THE TREATMENT OF FIBROSIS BRISTOL MYERS SQUIBB CO (US) 2024-11-13 EP claimed
US-12128026-B2 Selective androgen receptor degrader (SARD) ligands and methods of use thereof UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION (US) 2024-10-29 US disclosed
US-20240262838-A1 NITROGEN-CONTAINING HETEROCYCLIC COMPOUNDS AND USES THEREOF GUANGZHOU CHINARAY OPTOELECTRONIC MATERIALS LTD. (CN) 2024-08-08 US disclosed
EP-3286164-B1 SELECTIVE ANDROGEN RECEPTOR DEGRADER (SARD) LIGANDS AND METHODS OF USE THEREOF ONCTERNAL THERAPEUTICS INC (US) 2024-05-29 EP disclosed
CN-114644638-B Nitrogen-containing heterocyclic compound and application thereof 广州华睿光电材料有限公司 2024-04-23 CN disclosed
US-11873282-B2 Selective androgen receptor degrader (SARD) ligands and methods of use thereof UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION (US) 2024-01-16 US disclosed
US-20230416228-A1 AGENTS FOR THE TREATMENT OF DISEASES BY INHIBITION OF FOXO1 THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEWYORK 2023-12-28 US disclosed
CN-114621237-B Organic compounds, mixtures, compositions and organic electronic devices 广州华睿光电材料有限公司 2023-12-05 CN disclosed
US-11648234-B2 Selective androgen receptor degrader (SARD) ligands and methods of use UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION (US) 2023-05-16 US disclosed
CN-107709290-B Selective Androgen Receptor Degrader (SARD) ligands and methods of use thereof GTX公司 2023-02-28 CN disclosed
EP-2066316-A1 AZETIDINE AND AZETIDONE DERIVATIVES USEFUL IN TREATING PAIN AND DISORDERS OF LIPID METABOLISM SCHERING CORPORATION (US) 2009-06-10 EP disclosed
WO-2008033447-A1 AZETIDINE AND AZETIDONE DERIVATIVES USEFUL IN TREATING PAIN AND DISORDERS OF LIPID METABOLISM SCHERING CORPORATION (US) 2008-03-20 WO disclosed
US-20080070888-A1 AZETIDINE AND AZETIDONE DERIVATIVES USEFUL IN TREATING PAIN AND DISORDERS OF LIPID METABOLISM SCHERING CORPORATION 2008-03-20 US disclosed
US-20070269664-A1 Gas Barrier Laminated Film and Process for Producing the Same SAI NIPPON PRINTING CO., LTD. (JP) 2007-11-22 US disclosed
WO-2005108374-A1 INSECTICIDAL DIAZOLE AND TRIAZOLE DERIVATIVES FMC CORPORATION (US) 2005-11-17 WO disclosed
EP-0186190-B1 BENZIMIDAZOLE DERIVATIVES, AND THEIR PRODUCTION AND USE SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1993-05-26 EP disclosed
US-4663339-A Acaricidal and insecticidal substituted 1-phenylalkylbenzimidazoles SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1987-05-05 US disclosed
EP-0186190-A2 Benzimidazole derivatives, and their production and use SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1986-07-02 EP disclosed
US-3988155-A CYANINE SENSITIZING DYES FUJI PHOTO FILM CO., LTD. (JA) 1976-10-26 US disclosed
US-3985563-A Silver halide photographic emulsion FUJI PHOTO FILM CO., LTD. (JA) 1976-10-12 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 (7 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-20230416228-A1 AGENTS FOR THE TREATMENT OF DISEASES BY INHIBITION OF FOXO1 FOXO1, FOXO3, GCKR PARP1 1389/4885SMN1; SMN2 495/4885CA12 4667/4885
US-11648234-B2 Selective androgen receptor degrader (SARD) ligands and methods of use AR, BRCA1, FSHR PARP1 181/4885SMN1; SMN2 186/4885CA12 4341/4885
US-20070269664-A1 Gas Barrier Laminated Film and Process for Producing the Same CDH1, VIL1, TET1 PARP1 1997/4885SMN1; SMN2 3275/4885CA12 646/4885
US-20080070888-A1 AZETIDINE AND AZETIDONE DERIVATIVES USEFUL IN TREATING PAIN AND DISORDERS OF LIPID METABOLISM OPRD1, OPRK1, OPRL1 PARP1 3378/4885SMN1; SMN2 1682/4885CA12 4672/4885
US-20240262838-A1 NITROGEN-CONTAINING HETEROCYCLIC COMPOUNDS AND USES THEREOF NPR1, NPR3, NUCB2 PARP1 1264/4885SMN1; SMN2 2588/4885CA12 361/4885
US-12128026-B2 Selective androgen receptor degrader (SARD) ligands and methods of use thereof AR, AHR, BRDT PARP1 92/4885SMN1; SMN2 765/4885CA12 4816/4885
US-11873282-B2 Selective androgen receptor degrader (SARD) ligands and methods of use thereof AR, AHR, BRDT PARP1 92/4885SMN1; SMN2 765/4885CA12 4816/4885

“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.