SCHEMBL119741

SCHEMBL119741

O=C(O)CCC(=O)OC(CC(=O)O)(CC(=O)O)C(=O)O

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EGLN1 Q9GZT9 4/20 0.39
LMNA P02545 4/20 0.39
ALKBH5 Q6P6C2 1/20 0.39
SUCNR1 Q9BXA5 1/20 0.39
KDM6B O15054 2/20 0.39
KDM5C P41229 2/20 0.39
PHF8 Q9UPP1 2/20 0.39
KDM2A Q9Y2K7 2/20 0.39
ALDH1A1 P00352 2/20 0.36
TSHR P16473 2/20 0.35
CYP2D6 P10635 1/20 0.34
CYP2C19 P33261 1/20 0.34
HIF1A Q16665 1/20 0.34
SLC15A2 Q16348 1/20 0.32
MAPK1 P28482 1/20 0.32
SLC13A3 Q8WWT9 1/20 0.32
OR51E2 Q9H255 1/20 0.32
HMGCR P04035 1/20 0.31
CHRM1 P11229 1/20 0.31
TBXA2R P21731 1/20 0.31

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
Succinic Acid SCHEMBL8002651 1.00 EGLN1 (0.39) EGLN1LMNAALKBH5SUCNR1KDM6B
Succinic Acid SCHEMBL1871339 0.96 EGLN1 (0.36) EGLN1LMNAALKBH5SUCNR1KDM6B
SCHEMBL9241914 0.96 EGLN1 (0.36) EGLN1LMNAALKBH5SUCNR1KDM6B
SCHEMBL1989298 0.96 ALDH1A1 (0.39) EGLN1LMNAALKBH5SUCNR1KDM6B
SCHEMBL27076088 0.93 ALDH1A1 (0.37) EGLN1KDM6BKDM5CPHF8KDM2A
SCHEMBL28452924 0.93 ALDH1A1 (0.37) EGLN1KDM6BKDM5CPHF8KDM2A
SCHEMBL11245866 0.91 ALDH1A1 (0.36) EGLN1KDM6BKDM5CPHF8KDM2A
Pyruvate SCHEMBL14485736 0.91 EGLN1 (0.37) EGLN1LMNAALKBH5SUCNR1KDM6B
Succinic Acid SCHEMBL11064867 0.90 TSHR (0.46) LMNAALDH1A1TSHROR51E2SLC22A6
SCHEMBL5158691 0.89 LMNA (0.46) LMNAALDH1A1TSHRCYP2D6SLC22A6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117695279-A Loratadine composition and loratadine medicament 九华华源药业(桂林)有限公司 2024-03-15 CN claimed
EP-1878421-B1 EXTERNAL PREPARATION FOR SKIN SBI PHARMACEUTICALS CO LTD (JP) 2019-04-03 EP claimed
US-20120202891-A1 Cannabinoid-Containing Compositions and Methods for Their Use UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION (US) 2012-08-09 US claimed
EP-2424568-A1 CANNABINOID-CONTAINING COMPOSITIONS AND METHODS FOR THEIR USE University Of Kentucky Research Foundation (US) 2012-03-07 EP claimed
US-7939104-B2 Granulation; compaction; rapid dissolution upon contact with physiological solvents such as water, saliva or gastrointestinal fluids SANDOZ AG (CH) 2011-05-10 US claimed
WO-2010126501-A1 CANNABINOID-CONTAINING COMPOSITIONS AND METHODS FOR THEIR USE UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION (US) 2010-11-04 WO claimed
US-20080146581-A1 Solubility of hydrophobic drugs with a compound having a carboxylic acid moiety SANDOZ AG (CH) 2008-06-19 US claimed
US-20050249814-A1 Solubility of hydrophobic drugs with a compound having a carboxylic acid moiety SANDOZ AG (CH) 2005-11-10 US claimed
US-6825570-B2 Resistance-reducing conductive adhesives for attachment of electronic components MICRON TECHNOLOGY, INC. 2004-11-30 US claimed
US-20030044873-A1 Test strip for determining dialysate composition SERIM RESEARCH CORPORATION 2003-03-06 US claimed
CN-1088777-A The preparation method that is used for the chemotherapeutic preparation of directly administering to cancer nidus CONG FANZI (CN) 1994-07-06 CN claimed
US-5164307-A Biosynthesis AJINOMOTO CO., INC. (JP) 1992-11-17 US claimed
US-20230357220-A1 3-((1H-PYRAZOL-4-YL)METHYL)-6′-(PHENYL)-2H-(1,2′-BIPYRIDIN)-2-ONE DERIVATIVES AND RELATED COMPOUNDS AS GPR139 ANTAGONISTS FOR USE IN A METHOD OF TREATMENT OF E.G. DEPRESSION TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2023-11-09 US disclosed
US-20230348435-A1 1-((1H-PYRAZOL-4-YL)METHYL)-3-(PHENYL)-1,3-DIHYDRO-2H-IMIDAZOL-2-ONE DERIVATIVES AND RELATED COMPOUNDS AS GPR139 ANTAGONISTS FOR THE TREATMENT OF E.G. DEPRESSION TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2023-11-02 US disclosed
US-20230271974-A1 PROCESSES FOR THE PREPARATION OF (3S,4R)-3-ETHYL-4-(3H-IMIDAZO[1,2-a]PYRROLO[2,3-e]-PYRAZIN-8-YL)-N-(2,2,2-TRIFLUOROETHYL)PYRROLIDINE-1-CARBOXAMIDE AND SOLID STATE FORMS THEREOF ABBVIE INC. 2023-08-31 US disclosed
EP-4153583-A1 1-((1H-PYRAZOL-4-YL)METHYL)-3-(PHENYL)-1,3-DIHYDRO-2H-IMIDAZOL-2-ONE DERIVATIVES AND RELATED COMPOUNDS AS GPR139 ANTAGONISTS FOR THE TREATMENT OF E.G. DEPRESSION Takeda Pharmaceutical Company Limited (JP) 2023-03-29 EP disclosed
WO-1990014235-A1 HEAT-SENSITIVE RECORD MATERIAL SMITH & MCLAURIN LIMITED (GB) 1990-11-29 WO disclosed
EP-0399953-A2 Piperidine-triazine compounds for use as stabilizers for organic materials CIBA-GEIGY AG (CH) 1990-11-28 EP disclosed
EP-0395584-A2 Piperidine-triazine compounds for use as stabilizers for organic materials CIBA-GEIGY AG (CH) 1990-10-31 EP disclosed
US-4113858-A POLYPEPTIDES, MULTIPLE SCLEROSIS ST. LUKE'S HOSPITAL (US) 1978-09-12 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-20230271974-A1 PROCESSES FOR THE PREPARATION OF (3S,4R)-3-ETHYL-4-(3H-IMIDAZO[1,2-a]PYRROLO[2,3-e]-PYRAZIN-8-YL)-N-(2,2,2-TRIFLUOROETHYL)PYRROLIDINE-1-CARBOXAMIDE AND SOLID STATE FORMS THEREOF TSLP, HRH4, IL4 EGLN1 3103/4885LMNA 3035/4885ALKBH5 1961/4885
US-20080146581-A1 Solubility of hydrophobic drugs with a compound having a carboxylic acid moiety ABCG2, ABCB11, SLC10A1 EGLN1 3866/4885LMNA 4775/4885ALKBH5 4716/4885
US-20230348435-A1 1-((1H-PYRAZOL-4-YL)METHYL)-3-(PHENYL)-1,3-DIHYDRO-2H-IMIDAZOL-2-ONE DERIVATIVES AND RELATED COMPOUNDS AS GPR139 ANTAGONISTS FOR THE TREATMENT OF E.G. DEPRESSION GPR139, GPR142, HTR2C EGLN1 3176/4885LMNA 4728/4885ALKBH5 3707/4885
US-20230357220-A1 3-((1H-PYRAZOL-4-YL)METHYL)-6′-(PHENYL)-2H-(1,2′-BIPYRIDIN)-2-ONE DERIVATIVES AND RELATED COMPOUNDS AS GPR139 ANTAGONISTS FOR USE IN A METHOD OF TREATMENT OF E.G. DEPRESSION GPR139, GPR142, OPRL1 EGLN1 3973/4885LMNA 4725/4885ALKBH5 3920/4885
US-20120202891-A1 Cannabinoid-Containing Compositions and Methods for Their Use CNR2, CNR1, FAAH EGLN1 1500/4885LMNA 1856/4885ALKBH5 3968/4885
US-20050249814-A1 Solubility of hydrophobic drugs with a compound having a carboxylic acid moiety ABCG2, ABCB11, SLC10A1 EGLN1 3866/4885LMNA 4775/4885ALKBH5 4716/4885

“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.