SCHEMBL3438530

SCHEMBL3438530

CC(C)c1cccc(C(C)C)c1N1C(=O)c2ccc3c4ccc5c6c(ccc(c7ccc(c2c37)C1=O)c64)C(=O)N(c1c(C(C)C)cccc1C(C)C)C5=O

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ANPEP P15144 5/20 0.60
DPP4 P27487 5/20 0.60
NR1H2 P55055 1/20 0.55
NR1H3 Q13133 1/20 0.55
TERT O14746 2/20 0.40
NPC1 O15118 1/20 0.38
RAB9A P51151 1/20 0.38
STAT3 P40763 1/20 0.38
HIF1A Q16665 1/20 0.38
FAAH O00519 1/20 0.37
MGLL Q99685 1/20 0.37
LMNA P02545 2/20 0.36
TP53 P04637 2/20 0.36
L3MBTL1 Q9Y468 2/20 0.36
THRB P10828 1/20 0.36
TLR9 Q9NR96 1/20 0.36
MEN1 O00255 1/20 0.36
RGS12 O14924 1/20 0.36
USP2 O75604 1/20 0.36
MAPT P10636 1/20 0.36

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
SCHEMBL13478139 1.00 ANPEP (0.60) ANPEPDPP4NR1H2NR1H3TERT
SCHEMBL29461625 1.00 ANPEP (0.60) ANPEPDPP4NR1H2NR1H3TERT
SCHEMBL18071847 1.00 ANPEP (0.60) ANPEPDPP4NR1H2NR1H3TERT
SCHEMBL29369271 1.00 ANPEP (0.60) ANPEPDPP4NR1H2NR1H3TERT
SCHEMBL17151424 0.95 ANPEP (0.56) ANPEPDPP4NR1H2NR1H3TERT
SCHEMBL2607236 0.94 ANPEP (0.55) ANPEPDPP4NR1H2NR1H3TERT
SCHEMBL2704512 0.94 ANPEP (0.55) ANPEPDPP4NR1H2NR1H3TERT
SCHEMBL30954668 0.93 ANPEP (0.67) ANPEPDPP4NR1H2NR1H3NPC1
SCHEMBL17531021 0.93 ANPEP (0.67) ANPEPDPP4NR1H2NR1H3NPC1
SCHEMBL22334750 0.93 DPP4 (0.53) ANPEPDPP4NR1H2NR1H3LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7851628-B2 Conversion of perylene-3,4:9,10-tetracarboximides to a form suitable for use as fluorescent dyes BASF AKTIENGESELLSCHAFT (DE) 2010-12-14 US claimed
US-20090176985-A1 METHOD FOR CONVERTING PERYLEN-3,4:9,10-TETRACARBOXYLIC ACID DIIMIDES INTO A FORM SUITABLE FOR USE AS A FLUORESCENT DYE BASF SE (DE) 2009-07-09 US claimed
EP-1516018-B1 METHOD FOR CONVERTING PERYLEN-3,4:9,10-TETRACARBOXYLIC ACID DIIMIDES INTO A FORM SUITABLE FOR USE AS A FLUORESCENT DYE BASF AG (DE) 2005-11-23 EP claimed
US-20050251930-A1 Method for converting perylen-3,4:9,10-tetracarboxylic acid diimides into a form suitable for use as a fluorescent dye BASFAKTIENGESELLSCHAFT (DE) 2005-11-17 US claimed
US-6509188-B1 Solar radiation available is coupled in and can be distributed in such a way that all the microorganisms have an equally high photosynthesis activity regardless of position FRAUNHOFER-GESELLSCHAFT ZUR (DE) 2003-01-21 US claimed
EP-0862599-B1 FLUORESCENT DYE BLENDS MINNESOTA MINING & MFG (US) 2001-10-31 EP claimed
EP-0862599-A1 FLUORESCENT DYE BLENDS MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1998-09-09 EP claimed
US-5754337-A INCREASED VISIBILITY FOR TRAFFIC SIGNALS; BLENDS OF YELLOW PERYLENE DYE AND A YELLOW-GREEN DYE MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1998-05-19 US claimed
US-5672643-A FLUORESCENT YELLOW ARTICLE COMPRISING POLYOLEFIN OR OTHER POLYMER, PERYLENE IMIDE DYE, SELECTED YELLOW-GREEN DYE MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-09-30 US claimed
WO-1997012000-A1 FLUORESCENT DYE BLENDS MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-04-03 WO claimed
WO-2025242650-A1 SWITCHABLE ENCAPSULATED LUMINESCENT PIGMENTS GIESECKE+DEVRIENT CURRENCY TECHNOLOGY GMBH (DE) 2025-11-27 WO disclosed
WO-2025242649-A1 SYSTEM OF SWITCHABLE CAPSULE-LUMINESCENT PIGMENTS GIESECKE+DEVRIENT CURRENCY TECHNOLOGY GMBH (DE) 2025-11-27 WO disclosed
US-12018192-B2 Receiver comprising a luminescent collector for optical data communication BASF SE (DE) 2024-06-25 US disclosed
US-11873293-B2 Organic molecules for optoelectronic devices SAMSUNG DISPLAY CO., LTD. (KR) 2024-01-16 US disclosed
US-11873293-B2 Organic molecules for optoelectronic devices SAMSUNG DISPLAY CO., LTD. (KR) 2024-01-16 US disclosed
US-5754337-A INCREASED VISIBILITY FOR TRAFFIC SIGNALS; BLENDS OF YELLOW PERYLENE DYE AND A YELLOW-GREEN DYE MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1998-05-19 US disclosed
US-5672643-A FLUORESCENT YELLOW ARTICLE COMPRISING POLYOLEFIN OR OTHER POLYMER, PERYLENE IMIDE DYE, SELECTED YELLOW-GREEN DYE MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-09-30 US disclosed
US-5672643-A FLUORESCENT YELLOW ARTICLE COMPRISING POLYOLEFIN OR OTHER POLYMER, PERYLENE IMIDE DYE, SELECTED YELLOW-GREEN DYE MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-09-30 US disclosed
WO-1997012000-A1 FLUORESCENT DYE BLENDS MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-04-03 WO disclosed
WO-1997012000-A1 FLUORESCENT DYE BLENDS MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-04-03 WO 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 (2 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-20090176985-A1 METHOD FOR CONVERTING PERYLEN-3,4:9,10-TETRACARBOXYLIC ACID DIIMIDES INTO A FORM SUITABLE FOR USE AS A FLUORESCENT DYE C9, C1S, RCC1 ANPEP 2602/4885DPP4 4163/4885NR1H2 3768/4885
US-11873293-B2 Organic molecules for optoelectronic devices XDH, C1S, OR10J3 ANPEP 1394/4885DPP4 3308/4885NR1H2 231/4885

“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.