Sugi Predict

Sugi Predict / Compounds / SCHEMBL4857545

SCHEMBL4857545

SCHEMBL4857545

CN1C(=O)c2ccc3c4cccc5cccc(c6ccc(c2c36)C1=O)c54

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KMT2A Q03164 6/20 0.56
▸ MEN1 O00255 5/20 0.56
▸ USP2 O75604 2/20 0.56
▸ KEAP1 Q14145 2/20 0.56
▸ NFE2L2 Q16236 2/20 0.56
▸ KDM4E B2RXH2 2/20 0.56
▸ ALDH1A1 P00352 2/20 0.56
▸ HPGD P15428 2/20 0.56
▸ ATM Q13315 1/20 0.56
▸ POLB P06746 1/20 0.53
▸ PRMT1 Q99873 1/20 0.53
▸ TERT O14746 2/20 0.46
▸ STAT3 P40763 1/20 0.44
▸ HIF1A Q16665 1/20 0.44
▸ HSD17B10 Q99714 1/20 0.43
▸ CYP1B1 Q16678 1/20 0.43
▸ ERCC1 P07992 1/20 0.43
▸ FEN1 P39748 1/20 0.43
▸ ERCC4 Q92889 1/20 0.43
▸ HEXA P06865 3/20 0.41

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
SCHEMBL13009257 1.00 KMT2A (0.56) KMT2AMEN1USP2KEAP1NFE2L2
SCHEMBL12869514 0.87 KMT2A (0.57) KMT2AMEN1USP2KEAP1NFE2L2
SCHEMBL12449230 0.87 MEN1 (0.44) KMT2AMEN1USP2KEAP1NFE2L2
SCHEMBL29355182 0.87 TERT (0.56) KMT2AMEN1USP2KEAP1NFE2L2
SCHEMBL710594 0.87 TERT (0.56) KMT2AMEN1USP2KEAP1NFE2L2
SCHEMBL12170761 0.87 TERT (0.56) KMT2AMEN1USP2KEAP1NFE2L2
SCHEMBL9968962 0.87 TERT (0.56) KMT2AMEN1USP2KEAP1NFE2L2
SCHEMBL9968958 0.87 TERT (0.56) KMT2AMEN1USP2KEAP1NFE2L2
SCHEMBL12869518 0.84 KMT2A (0.63) KMT2AMEN1USP2KEAP1NFE2L2
SCHEMBL9968959 0.83 MEN1 (0.53) KMT2AMEN1USP2KEAP1NFE2L2

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-20220389310-A1 LUMINESCENT MATERIALS AND METHODS THEREOF UNIVERSITY OF WASHINGTON (US) 2022-12-08 — — US claimed
WO-2021062035-A1 LUMINESCENT MATERIALS AND METHODS THEREOF UNIVERSITY OF WASHINGTON (US) 2021-04-01 — — WO claimed
EP-3294811-B1 ULTRA BRIGHT DIMERIC OR POLYMERIC DYES SONY GROUP CORP (JP) 2024-02-28 — — EP disclosed
US-20220389310-A1 LUMINESCENT MATERIALS AND METHODS THEREOF UNIVERSITY OF WASHINGTON (US) 2022-12-08 — — US disclosed
WO-2021062035-A1 LUMINESCENT MATERIALS AND METHODS THEREOF UNIVERSITY OF WASHINGTON (US) 2021-04-01 — — WO disclosed
US-20200172489-A1 FLUORESCENT COMPOUND AND AUTOPHAGY DETECTION REAGENT USING SAME DOJINDO LABORATORIES (JP) 2020-06-04 — — US disclosed
US-9978951-B2 Perylene-based materials for organic photoelectric conversion layers SONY CORPORATION (JP) 2018-05-22 — — US disclosed
EP-2978820-B1 WAVELENGTH CONVERSION FILMS WITH MULTIPLE PHOTOSTABLE ORGANIC CHROMOPHORES NITTO DENKO CORP (JP) 2018-03-21 — — EP disclosed
US-9851359-B2 Ultra bright dimeric or polymeric dyes with spacing linker groups SONY CORPORATION OF AMERICA (US) 2017-12-26 — — US disclosed
US-20170292957-A1 ULTRA BRIGHT DIMERIC OR POLYMERIC DYES WITH SPACING LINKER GROUPS SONY CORPORATION (JP) 2017-10-12 — — US disclosed
US-9765220-B2 Water soluble fluorescent or colored dyes and methods for their use SONY CORPORATION (JP) 2017-09-19 — — US disclosed
US-7662308-B2 Polyhedral oligomeric silsesquioxane (POSS) based fluorescent colorants CIBA SPECIALTY CHEMICALS CORPORATION (US) 2010-02-16 — — US disclosed
US-20090099282-A1 Functionalized nanoparticles CIBA SPECIALTY CHEMICALS CORP. 2009-04-16 — — US disclosed
US-20080269482-A1 Use of Rylene Derivatives as Photosensitizers in Solar Cells BASF SE (DE) 2008-10-30 — — US disclosed
US-7358362-B2 Method for the production of terylene-3,4:11,12-tetracarboxydiimides by direct synthesis BASF AKTIENGESELLSCHAFT (DE) 2008-04-15 — — US disclosed
US-20080029739-A1 Novel polyhedral oligomeric silsesquioxane (POSS) based fluorescent colorants CIBA SPECIALTY CHEMICALS CORP. 2008-02-07 — — US disclosed
US-20070155968-A1 Method for the production of terylene-3,4:11,12-tetracarboxydiimides by direct synthesis BASF AKTIENGESELLSCHAFT (DE) 2007-07-05 — — US disclosed
US-6093834-A Preparation of perylene-3,4-dicarboxylic acid anhydrides CIBA SPECIALTY CHEMICALS CORPORATION (US) 2000-07-25 — — US disclosed
US-5900490-A Preparation of perylene-3, 4-Dicarboxylic acid anhydrides CIBA SPECIALTY CHEMICALS CORPORATION (US) 1999-05-04 — — US disclosed
US-5472494-A Coloring macromolecules BASF AKTIENGESELLSCHAFT (DE) 1995-12-05 — — 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 (4 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-20070155968-A1 Method for the production of terylene-3,4:11,12-tetracarboxydiimides by direct synthesis HACL2, HRH3, HCN2 KMT2A 717/4885MEN1 959/4885USP2 1927/4885
US-20220389310-A1 LUMINESCENT MATERIALS AND METHODS THEREOF TYR, GSTA2, CYBA KMT2A 1323/4885MEN1 1557/4885USP2 2124/4885
US-20080269482-A1 Use of Rylene Derivatives as Photosensitizers in Solar Cells NR2E3, NR2E1, NR1D2 KMT2A 940/4885MEN1 1376/4885USP2 3896/4885
US-20200172489-A1 FLUORESCENT COMPOUND AND AUTOPHAGY DETECTION REAGENT USING SAME NR2E3, GPR6, ATG13 KMT2A 2815/4885MEN1 3491/4885USP2 3711/4885

“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.