SCHEMBL757884

SCHEMBL757884

CCCC(=O)N(c1ccccc1)C(CCC(N)=O)C(=O)O

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TP53 P04637 2/20 0.48
LMNA P02545 3/20 0.40
ALDH1A1 P00352 2/20 0.40
SMN1; SMN2 Q16637 2/20 0.40
CES2 O00748 1/20 0.37
CES1 P23141 1/20 0.37
KMT2A Q03164 3/20 0.36
MMP2 P08253 2/20 0.36
MMP9 P14780 2/20 0.36
LTB4R2 Q9NPC1 2/20 0.36
MEN1 O00255 1/20 0.35
GLA P06280 1/20 0.35
TSHR P16473 1/20 0.35
OPRM1 P35372 1/20 0.35
OPRD1 P41143 1/20 0.35
OPRK1 P41145 1/20 0.35
TDP1 Q9NUW8 1/20 0.34
HSD17B10 Q99714 1/20 0.34
ALOX15 P16050 1/20 0.34
BLM P54132 1/20 0.34

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
SCHEMBL6535237 0.90 SMN1; SMN2 (0.41) TP53LMNAALDH1A1SMN1; SMN2KMT2A
SCHEMBL8429588 0.86 LMNA (0.39) TP53LMNAALDH1A1SMN1; SMN2KMT2A
SCHEMBL8429495 0.86 LMNA (0.39) TP53LMNAALDH1A1SMN1; SMN2KMT2A
SCHEMBL7342248 0.84 ALDH1A1 (0.40) TP53LMNAALDH1A1SMN1; SMN2KMT2A
SCHEMBL7342254 0.84 ALDH1A1 (0.40) TP53LMNAALDH1A1SMN1; SMN2KMT2A
SCHEMBL28294340 0.84 KMT2A (0.40) TP53LMNAALDH1A1SMN1; SMN2KMT2A
SCHEMBL7345170 0.83 MMP2 (0.40) TP53LMNAALDH1A1SMN1; SMN2KMT2A
SCHEMBL6464595 0.83 ALDH1A1 (0.39) TP53LMNAALDH1A1SMN1; SMN2KMT2A
SCHEMBL29033834 0.81 ALDH1A1 (0.40) TP53LMNAALDH1A1SMN1; SMN2KMT2A
SCHEMBL6930707 0.80 CTNNB1 (0.43) LMNAALDH1A1SMN1; SMN2TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2005053607-A2 METHOD FOR PREVENTING HEPATIC ENCEPHALOPATHIC EPISODES MEDICIS PHARMACEUTICAL CORPORATION (US) 2005-06-16 WO claimed
US-20040229948-A1 Method for preventing hepatic encephalopathic episodes MEDICIS PHARMACEUTICAL CORPORATION 2004-11-18 US claimed
US-20240041807-A1 COMBINATION THERAPY TO TREAT UREA CYCLE DISORDERS BAYLOR COLLEGE OF MEDICINE 2024-02-08 US disclosed
US-11819483-B2 Combination therapy to treat urea cycle disorders BAYLOR COLLEGE OF MEDICINE (US) 2023-11-21 US disclosed
US-20230181504-A1 COMBINATION THERAPY TO TREAT UREA CYCLE DISORDERS BAYLOR COLLEGE OF MEDICINE 2023-06-15 US disclosed
US-11517547-B2 Combination therapy to treat urea cycle disorders BAYLOR COLLEGE OF MEDICINE (US) 2022-12-06 US disclosed
US-20200170984-A1 COMBINATION THERAPY TO TREAT UREA CYCLE DISORDERS BAYLOR COLLEGE OF MEDICINE 2020-06-04 US disclosed
EP-3645053-A1 COMBINATION THERAPY TO TREAT UREA CYCLE DISORDERS Baylor College of Medicine (US) 2020-05-06 EP disclosed
WO-2019006164-A1 COMBINATION THERAPY TO TREAT UREA CYCLE DISORDERS BAYLOR COLLEGE OF MEDICINE (US) 2019-01-03 WO disclosed
US-9322893-B2 Methods of distinguishing between glutamine formed by cataplerosis or proteolysis BIOCANT-ASSOCIAÇÃO DE TRANSFERÊNCIA DE TECNOLOGIA (PT) 2016-04-26 US disclosed
EP-2286238-B1 METHODS OF DISTINGUISHING BETWEEN GLUTAMINE FORMED BY CATAPLEROSIS OR PROTEOLYSIS BIOCANT ASSOCIACAO DE TRANSFERENCIA DE TECNOLOGIA (PT) 2012-03-21 EP disclosed
US-20110079093-A1 Methods of Distinguishing Between Glutamine Formed by Cataplerosis or Proteolysis BIOCANT (PT) 2011-04-07 US disclosed
EP-2286238-A1 METHODS OF DISTINGUISHING BETWEEN GLUTAMINE FORMED BY CATAPLEROSIS OR PROTEOLYSIS Biocant - Associação De Transferência De Tecnologia (PT) 2011-02-23 EP disclosed
WO-2009141619-A1 METHODS OF DISTINGUISHING BETWEEN GLUTAMINE FORMED BY CATAPLEROSIS OR PROTEOLYSIS Biocant - Associação De Transferência De Tecnologia (PT) 2009-11-26 WO disclosed
WO-2005053607-A2 METHOD FOR PREVENTING HEPATIC ENCEPHALOPATHIC EPISODES MEDICIS PHARMACEUTICAL CORPORATION (US) 2005-06-16 WO disclosed
US-20040229948-A1 Method for preventing hepatic encephalopathic episodes MEDICIS PHARMACEUTICAL CORPORATION 2004-11-18 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 (1 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-20040229948-A1 Method for preventing hepatic encephalopathic episodes OAT, PYGL, SLC10A1 TP53 4406/4885LMNA 1753/4885ALDH1A1 1028/4885

“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.