SCHEMBL1874716

SCHEMBL1874716

NC(=O)[C@H](O)[C@@H](O)C(N)=O

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.42
ALDH1A1 P00352 2/20 0.42
OR51E2 Q9H255 1/20 0.42
TDP1 Q9NUW8 1/20 0.42
TSHR P16473 3/20 0.40
PGD P52209 1/20 0.40
HIF1A Q16665 1/20 0.39
ACHE P22303 1/20 0.39
BLM P54132 2/20 0.36
PMP22 Q01453 2/20 0.36
ALOX15 P16050 1/20 0.36
LDHA P00338 1/20 0.33
LDHB P07195 1/20 0.33
CYP3A4 P08684 2/20 0.31
NFKB1 P19838 2/20 0.31
HPGD P15428 1/20 0.31
EHMT2 Q96KQ7 1/20 0.31
HSD17B10 Q99714 1/20 0.31
EHMT1 Q9H9B1 1/20 0.31
CYP1A2 P05177 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
SCHEMBL7093505 1.00 LMNA (0.42) LMNAALDH1A1OR51E2TDP1TSHR
SCHEMBL77247 1.00 LMNA (0.42) LMNAALDH1A1OR51E2TDP1TSHR
SCHEMBL698993 0.86 TSHR (0.67) LMNAALDH1A1OR51E2TDP1TSHR
SCHEMBL1000048 0.84 PGD (0.37) LMNAALDH1A1OR51E2TDP1TSHR
SCHEMBL18902784 0.84 PGD (0.37) LMNAALDH1A1OR51E2TDP1TSHR
SCHEMBL987602 0.84 PGD (0.37) LMNAALDH1A1OR51E2TDP1TSHR
SCHEMBL4449219 0.84 PGD (0.37) LMNAALDH1A1OR51E2TDP1TSHR
SCHEMBL6686437 0.84 PGD (0.37) LMNAALDH1A1OR51E2TDP1TSHR
SCHEMBL18902700 0.83 PGD (0.33) LMNATSHRPGDHIF1ABLM
SCHEMBL18902557 0.83 LMNA (0.41) LMNATDP1TSHRPGDHIF1A

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
US-12127571-B2 Particulate acidulant composition comprising malic acid and lactic acid PURAC BIOCHEM B.V. (NL) 2024-10-29 US disclosed
CN-110743622-B Montmorillonite immobilized chiral compound and preparation method thereof 西安石油大学 2022-07-12 CN disclosed
EP-2116526-B1 DERIVATES OF SUBSTITUTED TARTARIC AICD AND USAGE FOR PREPARATING BETA SECRETASE INHIBITORS INST PHARMACOLOGY & TOXICOLOGY ACADEMY MILITARY MEDICAL SCIENCES PLA CHINA (CN) 2018-04-18 EP disclosed
WO-2015195563-A1 ANTIBACTERIAL AGENTS RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY (US) 2015-12-23 WO disclosed
US-8258345-B2 Hydroxylation of β-dicarbonyls with zirconium catalysts E I DU PONT DE NEMOURS AND COMPANY (US) 2012-09-04 US disclosed
US-20110196175-A1 Hydroxylation of Beta-Dicarbonyls with Zirconium Catalysts FMC CORPORATION 2011-08-11 US disclosed
US-7939685-B2 Hydroxylation of β-dicarbonyls with zirconium catalysts E. I. DU PONT DE NEMOURS AND COMPANY (US) 2011-05-10 US disclosed
US-20100185014-A1 Hydroxylation of Beta-Dicarbonyls with Zirconium Catalysts FMC CORPORATION 2010-07-22 US disclosed
US-7718818-B2 Hydroxylation of beta-dicarbonyls with zirconium catalysts E.I. DU PONT DE NEMOURS AND COMPANY (US) 2010-05-18 US disclosed
US-20080306259-A1 HYDROXYLATION OF BETA-DICARBONYLS WITH ZIRCONIUM CATALYSTS FMC CORPORATION 2008-12-11 US disclosed
US-7414157-B2 Hydroxylation of β-dicarbonyls with zirconium catalysts E. I. DU PONT DE NEMOURS AND COMPANY (US) 2008-08-19 US disclosed
US-7169544-B2 Thermally developable materials containing thermal solvents EASTMAN KODAK COMPANY (US) 2007-01-30 US disclosed
EP-1401575-B1 HYDROXYLATION OF BETA-DICARBONYLS WITH ZIRCONIUM CATALYSTS DU PONT (US) 2007-01-17 EP disclosed
US-20040143123-A1 Hydroxylation of beta-dicarbonyls with zirconium catalysts FMC CORPORATION 2004-07-22 US disclosed
EP-1401575-A1 HYDROXYLATION OF BETA-DICARBONYLS WITH ZIRCONIUM CATALYSTS E.I. DU PONT DE NEMOURS AND COMPANY (US) 2004-03-31 EP disclosed
WO-2003002255-A1 HYDROXYLATION OF BETA-DICARBONYLS WITH ZIRCONIUM CATALYSTS E.I. DU PONT DE NEMOURS AND COMPANY (US) 2003-01-09 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 (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-20100185014-A1 Hydroxylation of Beta-Dicarbonyls with Zirconium Catalysts CBR3, CBR1, NOXO1 LMNA 3105/4885ALDH1A1 258/4885OR51E2 1371/4885
US-20040143123-A1 Hydroxylation of beta-dicarbonyls with zirconium catalysts CBR1, CBR3, NOXO1 LMNA 3661/4885ALDH1A1 163/4885OR51E2 1879/4885
US-20110196175-A1 Hydroxylation of Beta-Dicarbonyls with Zirconium Catalysts CBR3, CBR1, NOXO1 LMNA 3105/4885ALDH1A1 258/4885OR51E2 1371/4885
US-20080306259-A1 HYDROXYLATION OF BETA-DICARBONYLS WITH ZIRCONIUM CATALYSTS CBR3, CBR1, ASPH LMNA 3881/4885ALDH1A1 260/4885OR51E2 809/4885

“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.