SCHEMBL6307083

SCHEMBL6307083

CC(O)C(=O)NCC(=O)O

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.64
MAPT P10636 2/20 0.64
LMNA P02545 1/20 0.64
PTGS2 P35354 1/20 0.64
TDP1 Q9NUW8 1/20 0.64
ECE1 P42892 2/20 0.55
MME P08473 6/20 0.53
ACE P12821 4/20 0.53
CPA1 P15085 1/20 0.53
ACE2 Q9BYF1 1/20 0.53
MEN1 O00255 2/20 0.48
KMT2A Q03164 2/20 0.48
EGLN1 Q9GZT9 2/20 0.43
TP53 P04637 1/20 0.41
CTH P32929 1/20 0.39
FAAH O00519 1/20 0.38
HPGD P15428 1/20 0.38
MAPK1 P28482 1/20 0.38
HSD17B10 Q99714 1/20 0.38
BLM P54132 1/20 0.38

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
(Isobutyrylamino)Acetic Acid SCHEMBL622544 0.82 ALDH1A1 (0.67) ALDH1A1MAPTLMNAPTGS2TDP1
SCHEMBL22807661 0.81 ALDH1A1 (0.59) ALDH1A1MAPTLMNAPTGS2TDP1
SCHEMBL13429289 0.81 ALDH1A1 (0.59) ALDH1A1MAPTLMNAPTGS2TDP1
SCHEMBL1644159 0.81 ALDH1A1 (0.59) ALDH1A1MAPTLMNAPTGS2TDP1
SCHEMBL6307075 0.80 ALDH1A1 (0.64) ALDH1A1MAPTLMNAPTGS2TDP1
SCHEMBL5853497 0.79
SCHEMBL23880757 0.79 ALDH1A1 (0.52) ALDH1A1MAPTLMNAPTGS2TDP1
SCHEMBL17037463 0.78 ALDH1A1 (0.61) ALDH1A1MAPTLMNAPTGS2TDP1
Tiopronin SCHEMBL3009491 0.78 ALDH1A1 (1.00) ALDH1A1MAPTLMNAPTGS2TDP1
SCHEMBL3008983 0.78 ALDH1A1 (0.61) ALDH1A1MAPTLMNAPTGS2TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116444388-B Method for preparing morpholine-2, 5-dione monomer by polylactic acid ammonolysis 中国科学院青岛生物能源与过程研究所 2024-06-14 CN claimed
CN-116444388-A Method for preparing morpholine-2, 5-dione monomer by polylactic acid ammonolysis 中国科学院青岛生物能源与过程研究所 2023-07-18 CN claimed
US-6906058-B2 1,5-Benzothiazepines and their use as hypolipidaemics ASTRAZENECA AB (SE) 2005-06-14 US claimed
EP-0804181-A4 METHOD AND COMPOSITION FOR TREATING MAMMALIAN DISEASES CAUSED BY INFLAMMATORY RESPONSE CELLULAR SCIENCES INC (US) 2005-02-02 EP claimed
EP-1263747-B1 1,5-BENZOTHIAZEPINES AND THEIR USE AS HYPOLIPIDAEMICS ASTRAZENECA AB (SE) 2004-11-24 EP claimed
US-20030166927-A1 1,5-Benzothiazepines and their use as hypolipidaemics ALBIREO AB (SE) 2003-09-04 US claimed
EP-0804181-A1 METHOD AND COMPOSITION FOR TREATING MAMMALIAN DISEASES CAUSED BY INFLAMMATORY RESPONSE Cellular Sciences, Inc. (US) 1997-11-05 EP claimed
WO-1997010818-A1 METHOD AND COMPOSITION FOR TREATING MAMMALIAN DISEASES CAUSED BY INFLAMMATORY RESPONSE CELLULAR SCIENCES, INC. (US) 1997-03-27 WO claimed
CN-116444388-B Method for preparing morpholine-2, 5-dione monomer by polylactic acid ammonolysis 中国科学院青岛生物能源与过程研究所 2024-06-14 CN disclosed
CN-116444388-B Method for preparing morpholine-2, 5-dione monomer by polylactic acid ammonolysis 中国科学院青岛生物能源与过程研究所 2024-06-14 CN disclosed
CN-116444388-A Method for preparing morpholine-2, 5-dione monomer by polylactic acid ammonolysis 中国科学院青岛生物能源与过程研究所 2023-07-18 CN disclosed
CN-116444388-A Method for preparing morpholine-2, 5-dione monomer by polylactic acid ammonolysis 中国科学院青岛生物能源与过程研究所 2023-07-18 CN disclosed
US-6906058-B2 1,5-Benzothiazepines and their use as hypolipidaemics ASTRAZENECA AB (SE) 2005-06-14 US disclosed
EP-0804181-A4 METHOD AND COMPOSITION FOR TREATING MAMMALIAN DISEASES CAUSED BY INFLAMMATORY RESPONSE CELLULAR SCIENCES INC (US) 2005-02-02 EP disclosed
WO-2001066533-A1 1,5-BENZOTHIAZEPINES AND THEIR USE AS HYPOLIPIDAEMICS ASTRAZENECA AB (SE) 2001-09-13 WO disclosed
US-5952384-A CONTACTING THE MAMMALIAN CELL WITH AN INFLAMMATORY MEDIATOR SELECTED FROM THE GROUP CONSISTS OF PYRUVATE AND PYRUVATE PRECURSOR CAPABLE OF REDUCING UNDESIRED INFLAMMATORY RESPONSE AND IS ANTIOXIDANT CELLULAR SCIENCES, INC. (US) 1999-09-14 US disclosed
US-5939459-A CONTACTING WITH AN INFLAMMATORY MEDIATOR SELECTED FROM THE GROUP CONSISTING OF PYRUVATE AND A PYRUVATE PRECURSOR AND IS PRESENT IN AN AMOUNT CAPABLE OF REDUCING THE UNDESIRED INFLAMMATORY RESPONSE AND IS AN ANTIOXIDANT CELLULAR SCIENCES INC. (US) 1999-08-17 US disclosed
US-5798388-A ANTIOXIDANT, ANTIASTHMA, ADMINISTERING PYRUVATE WITHOUT ALBUTEROL CELLULAR SCIENCES, INC. (US) 1998-08-25 US disclosed
EP-0804181-A1 METHOD AND COMPOSITION FOR TREATING MAMMALIAN DISEASES CAUSED BY INFLAMMATORY RESPONSE Cellular Sciences, Inc. (US) 1997-11-05 EP disclosed
WO-1997010818-A1 METHOD AND COMPOSITION FOR TREATING MAMMALIAN DISEASES CAUSED BY INFLAMMATORY RESPONSE CELLULAR SCIENCES, INC. (US) 1997-03-27 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 (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-20030166927-A1 1,5-Benzothiazepines and their use as hypolipidaemics SLC10A2, SLC10A1, LCAT ALDH1A1 811/4885MAPT 1147/4885LMNA 2733/4885

“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.