SCHEMBL8847697

SCHEMBL8847697

CCCCC(=O)NCCC(C)C

nearest known ligand 0.67

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
CNR1 P21554 2/20 0.67
LMNA P02545 1/20 0.57
PKM P14618 1/20 0.57
HPGD P15428 1/20 0.54
CASP2 P42575 1/20 0.52
FAAH O00519 5/20 0.52
DNM1 Q05193 2/20 0.49
NAAA Q02083 1/20 0.48
ALDH1A1 P00352 1/20 0.48
PSMB5 P28074 1/20 0.47
NAMPT P43490 1/20 0.46
LPAR2 Q9HBW0 1/20 0.46
MEN1 O00255 1/20 0.46
MAPK1 P28482 1/20 0.46
KMT2A Q03164 1/20 0.46
PLA2G10 O15496 1/20 0.45

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
SCHEMBL17125686 0.94 CNR1 (0.69) CNR1LMNAPKMHPGDCASP2
SCHEMBL5866922 0.92 CNR1 (0.68) CNR1LMNAPKMCASP2FAAH
SCHEMBL1456865 0.92 CNR1 (0.68) CNR1LMNAPKMCASP2FAAH
SCHEMBL1456478 0.92 CNR1 (0.68) CNR1LMNAPKMCASP2FAAH
SCHEMBL1695972 0.92 CNR1 (0.68) CNR1LMNAPKMCASP2FAAH
SCHEMBL20206555 0.90 CNR1 (0.56) CNR1LMNAPKMHPGDCASP2
SCHEMBL19249120 0.89 CASP2 (0.58) CNR1LMNAPKMCASP2FAAH
SCHEMBL21727959 0.88 CNR1 (0.55) CNR1LMNAPKMHPGDCASP2
SCHEMBL13328249 0.88 LMNA (0.60) CNR1LMNAPKMHPGDFAAH
SCHEMBL8847608 0.88 CNR1 (0.57) CNR1LMNAPKMHPGDCASP2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11685714-B2 Prodrugs of cytotoxic active agents having enzymatically cleavable groups BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2023-06-27 US disclosed
US-20230160000-A1 SYNTHESIS OF NOVEL DISULFIDE LINKER BASED NUCLEOTIDES AS REVERSIBLE TERMINATORS FOR DNA SEQUENCING BY SYNTHESIS THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2023-05-25 US disclosed
WO-2023018743-A1 PH-RESPONSIVE NANOPARTICLE FOR DELIVERY OF RIBONUCLEOPROTEINS WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2023-02-16 WO disclosed
US-10450307-B2 Compounds having estrogen receptor alpha degradation activity and uses thereof ACCUTAR BIOTECHNOLOGY INC. (US) 2019-10-22 US disclosed
US-20190134214-A1 GLP-1 Receptor Ligand Moiety Conjugated Oligonucleotides and Uses Thereof ASTRAZENECA AB (SE) 2019-05-09 US disclosed
US-20190077752-A1 PRODRUGS OF CYTOTOXIC ACTIVE AGENTS HAVING ENZYMATICALLY CLEAVABLE GROUPS BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2019-03-14 US disclosed
US-20180208590-A1 NOVEL COMPOUNDS HAVING ESTROGEN RECEPTOR ALPHA DEGRADATION ACTIVITY AND USES THEREOF ACCUTAR BIOTECHNOLOGY INC. (US) 2018-07-26 US disclosed
EP-1615925-B1 IMIDAZOPYRIDINE DERIVATIVES AS MELANOCORTIN RECEPTOR AGONISTS IPSEN PHARMA (FR) 2009-05-27 EP disclosed
US-7495009-B2 Imidazopyridine derivatives as melancortin receptor agonists SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES (S.C.R.A.S.) (FR) 2009-02-24 US disclosed
US-7495009-B2 Imidazopyridine derivatives as melancortin receptor agonists SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES (S.C.R.A.S.) (FR) 2009-02-24 US disclosed
US-5614519-A (1-(2,3 or 4-N-morpholinoalkyl)-imidazol-4-yl)-benizimidazol-1-yl-methyl]-biphenyls useful as angiotensin-II antagonists KARL THOMAE GMBH (DE) 1997-03-25 US disclosed
US-5602127-A ADMINISTERING TO TREAT HYPERTENSION KARL THOMAE GMBH (DE) 1997-02-11 US disclosed
US-5594003-A HYPOTENSIVE AGENTS DR. KARL THOMAE GMBH (DE) 1997-01-14 US disclosed
US-5591762-A HYPOTENSIVE AGENTS DR. KARL THOMAE GMBH (DE) 1997-01-07 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 (6 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-10450307-B2 Compounds having estrogen receptor alpha degradation activity and uses thereof ESR2, ESRRG, ESR1 CNR1 487/4885LMNA 1648/4885PKM 2868/4885
US-20190134214-A1 GLP-1 Receptor Ligand Moiety Conjugated Oligonucleotides and Uses Thereof GLP1R, GIPR, GRPR CNR1 785/4885LMNA 3766/4885PKM 3869/4885
US-11685714-B2 Prodrugs of cytotoxic active agents having enzymatically cleavable groups BUB1B, KIF5B, TK1 CNR1 4712/4885LMNA 552/4885PKM 779/4885
US-20180208590-A1 NOVEL COMPOUNDS HAVING ESTROGEN RECEPTOR ALPHA DEGRADATION ACTIVITY AND USES THEREOF ESR2, ESRRG, ESR1 CNR1 520/4885LMNA 2029/4885PKM 2946/4885
US-20190077752-A1 PRODRUGS OF CYTOTOXIC ACTIVE AGENTS HAVING ENZYMATICALLY CLEAVABLE GROUPS BUB1B, KIF5B, TK1 CNR1 4712/4885LMNA 552/4885PKM 779/4885
US-20230160000-A1 SYNTHESIS OF NOVEL DISULFIDE LINKER BASED NUCLEOTIDES AS REVERSIBLE TERMINATORS FOR DNA SEQUENCING BY SYNTHESIS POLRMT, RNGTT, MTR CNR1 4514/4885LMNA 984/4885PKM 3821/4885

“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.