SCHEMBL3120664

SCHEMBL3120664

CCCCCCC[CH]N(CC)CC

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.46
THRB P10828 1/20 0.42
FAAH O00519 2/20 0.41
TRPV1 Q8NER1 1/20 0.41
DNM1 Q05193 4/20 0.39
EP300 Q09472 1/20 0.37
GMNN O75496 1/20 0.35
USP2 O75604 1/20 0.35
LMNA P02545 1/20 0.35
CYP1A2 P05177 1/20 0.35
POLB P06746 1/20 0.35
MAPT P10636 1/20 0.35
CYP2C9 P11712 1/20 0.35
ALOX15 P16050 1/20 0.35
APEX1 P27695 1/20 0.35
CYP2C19 P33261 1/20 0.35
RECQL P46063 1/20 0.35
BLM P54132 1/20 0.35
NPSR1 Q6W5P4 1/20 0.35
HSD17B10 Q99714 1/20 0.35

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
SCHEMBL5145378 1.00 TSHR (0.46) TSHRTHRBFAAHTRPV1DNM1
SCHEMBL5648168 1.00 TSHR (0.46) TSHRTHRBFAAHTRPV1DNM1
SCHEMBL25378343 1.00 TSHR (0.46) TSHRTHRBFAAHTRPV1DNM1
SCHEMBL639750 0.97 TSHR (0.42) TSHRTHRBFAAHTRPV1DNM1
SCHEMBL318154 0.89 TSHR (0.41) TSHRTHRBDNM1LMNA
SCHEMBL8318187 0.82 DNM1 (0.46) TSHRTHRBFAAHTRPV1DNM1
SCHEMBL317337 0.82 TSHR (0.44) TSHRTHRBFAAHTRPV1DNM1
SCHEMBL8321451 0.82 DNM1 (0.46) TSHRTHRBFAAHTRPV1DNM1
SCHEMBL1405657 0.82 DNM1 (0.46) TSHRTHRBFAAHTRPV1DNM1
SCHEMBL5958083 0.82 TSHR (0.44) TSHRTHRBFAAHTRPV1DNM1

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 13 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4355794-A1 FREE-RADICALLY POLYMERIZABLE COPOLYMER, FREE-RADICALLY POLYMERIZABLE COMPOSITION CONTAINING THE SAME, AND POLYMERIZED REACTION PRODUCT THEREFROM 3M Innovative Properties Company (US) 2024-04-24 EP disclosed
WO-2022263987-A1 FREE-RADICALLY POLYMERIZABLE COPOLYMER, FREE-RADICALLY POLYMERIZABLE COMPOSITION CONTAINING THE SAME, AND POLYMERIZED REACTION PRODUCT THEREFROM 3M INNOVATIVE PROPERTIES COMPANY (US) 2022-12-22 WO disclosed
EP-2016939-B1 TRANSDERMALLY ABSORBABLE PREPARATION COMPRISING ANTI-DEMENTIA AGENT TEIKOKU SEIYAKU KK (JP) 2014-03-19 EP disclosed
US-20110059141-A1 PERCUTANEOUS ABSORPTION PREPARATIONS OF ANTIDEMENTIA DRUGS ITO TAKESHI 2011-03-10 US disclosed
US-7858114-B2 used as plaster on skin; comprises adherent layer, intermediate membrane, and drug reservoir layer sequentially from skin side, wherein drug reservoir layer comprises an antidementia drug, an aminated polymer, a polyhydric alcohol, and carboxylic acid esters TEIKOKU SEIYAKU CO., LTD. (JP) 2010-12-28 US disclosed
US-20100178307-A1 TRANSDERMAL ANTI-DEMENTIA ACTIVE AGENT FORMULATIONS AND METHODS FOR USING THE SAME TEIKOKU PHARMA USA INC. 2010-07-15 US disclosed
EP-2016939-A1 TRANSDERMALLY ABSORBABLE PREPARATION COMPRISING ANTI-DEMENTIA AGENT TEIKOKU SEIYAKU CO., LTD. (JP) 2009-01-21 EP disclosed
US-7301029-B2 Bipyridine Derivatives FUJIFILM FINECHEMICALS CO., LTD. (JP) 2007-11-27 US disclosed
US-20070259028-A1 used as plaster on skin; comprises adherent layer, intermediate membrane, and drug reservoir layer sequentially from skin side, wherein drug reservoir layer comprises an antidementia drug, an aminated polymer, a polyhydric alcohol, and carboxylic acid esters TEIKOKU SEIYAKU CO., LTD. (JP) 2007-11-08 US disclosed
US-7276600-B2 Phthalocyanine derivatives and their applications in optical recording media TSAI YEN CHENG 2007-10-02 US disclosed
US-20060292494-A1 Novel phthalocyanine derivatives, synthetic process thereof and their applications in optical recording media TSAI YEN C 2006-12-28 US disclosed
US-20060281026-A1 Phthalocyanine derivatives and their applications in optical recording media TSAI YEN C 2006-12-14 US disclosed
US-20050085642-A1 Novel bipyridine derivatives SANKIO CHEMICAL CO., LTD. 2005-04-21 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-20050085642-A1 Novel bipyridine derivatives PFAS, CBR3, Q6ZSR9 TSHR 726/4885THRB 1975/4885FAAH 4059/4885
US-20060292494-A1 Novel phthalocyanine derivatives, synthetic process thereof and their applications in optical recording media TRPC3, TRPA1, TRPC6 TSHR 2593/4885THRB 1173/4885FAAH 4818/4885
US-20060281026-A1 Phthalocyanine derivatives and their applications in optical recording media CRY2, CACNA1C, CRY1 TSHR 3982/4885THRB 2759/4885FAAH 3539/4885
US-20100178307-A1 TRANSDERMAL ANTI-DEMENTIA ACTIVE AGENT FORMULATIONS AND METHODS FOR USING THE SAME ACHE, CHAT, GAP43 TSHR 4744/4885THRB 4117/4885FAAH 350/4885

“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.