SCHEMBL2861936

SCHEMBL2861936

O=C1c2ccc3c4ccc5c6c(ccc(c7ccc(c2c37)C(=O)N1C1CCCCC1)c64)C(=O)N(C1CCCCC1)C5=O

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 11/20 0.51
KDM4E B2RXH2 3/20 0.49
HPGD P15428 3/20 0.49
HSD17B10 Q99714 3/20 0.49
SMN1; SMN2 Q16637 3/20 0.49
ATM Q13315 1/20 0.49
NPSR1 Q6W5P4 1/20 0.49
TERT O14746 3/20 0.49
MAPK1 P28482 2/20 0.46
KMT2A Q03164 3/20 0.43
MEN1 O00255 2/20 0.43
LMNA P02545 1/20 0.43
GAA P10253 1/20 0.43
MAPT P10636 1/20 0.43
STAT3 P40763 1/20 0.43
TDP1 Q9NUW8 1/20 0.43
CYP3A4 P08684 1/20 0.42
CYP2C9 P11712 1/20 0.42
CYP2C19 P33261 1/20 0.42
NPC1 O15118 1/20 0.40

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
SCHEMBL6266985 1.00 ALDH1A1 (0.51) ALDH1A1KDM4EHPGDHSD17B10SMN1; SMN2
SCHEMBL822758 0.98 ALDH1A1 (0.49) ALDH1A1KDM4EHPGDHSD17B10SMN1; SMN2
SCHEMBL10261468 0.92 ALDH1A1 (0.57) ALDH1A1KDM4EHPGDHSD17B10SMN1; SMN2
SCHEMBL10260482 0.92 ALDH1A1 (0.57) ALDH1A1KDM4EHPGDHSD17B10SMN1; SMN2
SCHEMBL13001996 0.91 ALDH1A1 (0.48) ALDH1A1KDM4EHPGDHSD17B10SMN1; SMN2
SCHEMBL12511989 0.90 ALDH1A1 (0.56) ALDH1A1KDM4EHPGDHSD17B10SMN1; SMN2
SCHEMBL822463 0.90 ALDH1A1 (0.54) ALDH1A1KDM4EHPGDHSD17B10SMN1; SMN2
SCHEMBL15247068 0.90 ALDH1A1 (0.43) ALDH1A1KDM4EHPGDHSD17B10SMN1; SMN2
SCHEMBL8878000 0.89 ALDH1A1 (0.47) ALDH1A1KDM4EHPGDHSD17B10SMN1; SMN2
SCHEMBL4859288 0.89 ALDH1A1 (0.47) ALDH1A1KDM4EHPGDHSD17B10SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11912720-B2 Rigid chiral photoluminescent isosceles triangular materials NORTHWESTERN UNIVERSITY (US) 2024-02-27 US disclosed
US-11022592-B2 Chemical self-doping of one-dimensional organic nanomaterials for high conductivity application in chemiresistive sensing gas or vapor UNIVERSITY OF UTAH RESEARCH FOUNDATION (US) 2021-06-01 US disclosed
EP-3383876-A2 CHEMICAL SELF-DOPING OF ONE-DIMENSIONAL ORGANIC NANOMATERIALS FOR HIGH CONDUCTIVITY APPLICATION IN CHEMIRESISTIVE SENSING GAS OR VAPOR University of Utah Research Foundation (US) 2018-10-10 EP disclosed
WO-2017142609-A2 CHEMICAL SELF-DOPING OF ONE-DIMENSIONAL ORGANIC NANOMATERIALS FOR HIGH CONDUCTIVITY APPLICATION IN CHEMIRESISTIVE SENSING GAS OR VAPOR UNIVERSITY OF UTAH RESEARCH FOUNDATION (US) 2017-08-24 WO disclosed
US-9701784-B2 Supramolecular polymers derived from perylene-diimides YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) 2017-07-11 US disclosed
US-9701784-B2 Supramolecular polymers derived from perylene-diimides YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) 2017-07-11 US disclosed
US-20170160252-A1 CHEMICAL SELF-DOPING OF ONE-DIMENSIONAL ORGANIC NANOMATERIALS FOR HIGH CONDUCTIVITY APPLICATION IN CHEMIRSISTIVE SENSING GAS OR VAPOR UNIVERSITY OF UTAH 2017-06-08 US disclosed
EP-3067354-A1 SUPRAMOLECULAR POLYMERS DERIVED FROM PERYLENE-DIIMIDES Yeda Research and Development Co. Ltd. (IL) 2016-09-14 EP disclosed
US-20150240027-A1 SUPRAMOLECULAR POLYMERS DERIVED FROM PERYLENE-DIIMIDES YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) 2015-08-27 US disclosed
US-20150240027-A1 SUPRAMOLECULAR POLYMERS DERIVED FROM PERYLENE-DIIMIDES YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) 2015-08-27 US disclosed
EP-2155741-A2 SELECTIVE BROMINATION OF PERYLENE DIIMIDES AND DERIVATIVES THEREOF UNDER MILD CONDITIONS Yeda Research And Development Co. Ltd. (IL) 2010-02-24 EP disclosed
WO-2009118742-A1 DOUBLY REDUCED PERYLENE-DIIMIDES AND SUPRAMOLECULAR POLYMERS DERIVED FROM PERYLENE-DIIMIDES YEDA RESEARCH AND DEVELOPMENT CO. LTD (IL) 2009-10-01 WO disclosed
WO-2009024512-A1 HALOGEN-CONTAINING PERYLENETETRACARBOXYLIC ACID DERIVATIVES AND THE USE THEREOF BASF SE (DE) 2009-02-26 WO disclosed
WO-2008139452-A2 SELECTIVE BROMINATION OF PERYLENE DIIMIDES AND DERIVATIVES THEREOF UNDER MILD CONDITIONS YEDA RESEARCH AND DEVELOPMENT CO.LTD (IL) 2008-11-20 WO disclosed
US-20080161569-A1 PREPARATION OF PERYLEN-3,4:9,10-TETRACARBOXYLIC DIANHYDRIDE AND ALSO OF NAPHTALENE-1,8-DICARBOXIMIDES BASF AKTIENGESELLSCHAFT (DE) 2008-07-03 US disclosed
US-7393956-B2 Method for the production of perylen-3,4:9,10-tetracarboxylic acid diimides and perylen-3,4:9,10-tetracarboxylic acid dianhydride and naphtalene-1,8-dicarboxylimides BASF AKTIENGESELLSCHAFT (DE) 2008-07-01 US disclosed
US-20080087878-A1 USE OF PERYLENE DIIMIDE DERIVATIVES AS AIR-STABLE N-CHANNEL ORGANIC SEMICONDUCTORS BASF AKIENGESELLSCHAFT (DE) 2008-04-17 US disclosed
US-20080054258-A1 USE OF PERYLENE DIIMIDE DERIVATIVES AS AIR-STABLE N-CHANNEL ORGANIC SEMICONDUCTORS BASF AKTIENGESELLSCHAFT (DE) 2008-03-06 US disclosed
US-20080035914-A1 Use of perylene diimide derivatives as air-stable n-channel organic semiconductors BASF AKTIENGESELLSCHAFT (DE) 2008-02-14 US disclosed
US-20050131220-A1 Method for the production of perylen-3,4:9,10-tetracarboxylic acid diimides and perylen-3,4:9,10-tetracarboxylic acid dianhydride and naphtalene-1,8-dicarboxylimides BASF AKTIENGESELLSCHAFT (DE) 2005-06-16 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 (9 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-20080161569-A1 PREPARATION OF PERYLEN-3,4:9,10-TETRACARBOXYLIC DIANHYDRIDE AND ALSO OF NAPHTALENE-1,8-DICARBOXIMIDES CLIC1, PNPO, CLIC4 ALDH1A1 1464/4885KDM4E 2769/4885HPGD 1064/4885
US-20080035914-A1 Use of perylene diimide derivatives as air-stable n-channel organic semiconductors KCNN2, CACNA1B, HCN4 ALDH1A1 3133/4885KDM4E 1272/4885HPGD 3802/4885
US-20170160252-A1 CHEMICAL SELF-DOPING OF ONE-DIMENSIONAL ORGANIC NANOMATERIALS FOR HIGH CONDUCTIVITY APPLICATION IN CHEMIRSISTIVE SENSING GAS OR VAPOR DRD1, DRD4, DNER ALDH1A1 244/4885KDM4E 2247/4885HPGD 3104/4885
US-20080087878-A1 USE OF PERYLENE DIIMIDE DERIVATIVES AS AIR-STABLE N-CHANNEL ORGANIC SEMICONDUCTORS KCNN2, HCN4, CACNA1B ALDH1A1 3024/4885KDM4E 1229/4885HPGD 3682/4885
US-11912720-B2 Rigid chiral photoluminescent isosceles triangular materials PPIE, PARN, PIN1 ALDH1A1 1708/4885KDM4E 1234/4885HPGD 251/4885
US-20150240027-A1 SUPRAMOLECULAR POLYMERS DERIVED FROM PERYLENE-DIIMIDES PIN1, PARN, DDT ALDH1A1 2069/4885KDM4E 2710/4885HPGD 2025/4885
US-20050131220-A1 Method for the production of perylen-3,4:9,10-tetracarboxylic acid diimides and perylen-3,4:9,10-tetracarboxylic acid dianhydride and naphtalene-1,8-dicarboxylimides CBR1, CBR3, SCO2 ALDH1A1 2188/4885KDM4E 4636/4885HPGD 1416/4885
US-11022592-B2 Chemical self-doping of one-dimensional organic nanomaterials for high conductivity application in chemiresistive sensing gas or vapor DRD1, DRD2, DNER ALDH1A1 323/4885KDM4E 2229/4885HPGD 3219/4885
US-20080054258-A1 USE OF PERYLENE DIIMIDE DERIVATIVES AS AIR-STABLE N-CHANNEL ORGANIC SEMICONDUCTORS KCNN2, CACNA1B, HCN4 ALDH1A1 3133/4885KDM4E 1272/4885HPGD 3802/4885

“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.