SCHEMBL125700

SCHEMBL125700

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

nearest known ligand 0.60

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 0.60
SLC22A6 Q4U2R8 1/20 0.50
GABRR1 P24046 2/20 0.42
LMNA P02545 1/20 0.42
TDP1 Q9NUW8 1/20 0.41
TET2 Q6N021 6/20 0.39
TET3 O43151 2/20 0.39
TET1 Q8NFU7 1/20 0.39
MAPT P10636 1/20 0.37
KDM4A O75164 2/20 0.36
KDM4C Q9H3R0 2/20 0.36
KDM2A Q9Y2K7 2/20 0.36
TSHR P16473 1/20 0.35
OR51E2 Q9H255 1/20 0.35
GPR84 Q9NQS5 2/20 0.33

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
SCHEMBL8416906 1.00 SMN1; SMN2 (0.60) SMN1; SMN2SLC22A6GABRR1LMNATDP1
SCHEMBL8417005 1.00 SMN1; SMN2 (0.60) SMN1; SMN2SLC22A6GABRR1LMNATDP1
Malic Acid SCHEMBL6863763 0.77 SMN1; SMN2 (0.88) SMN1; SMN2SLC22A6GABRR1LMNATDP1
SCHEMBL19912995 0.76 OR51E2 (0.36) SMN1; SMN2SLC22A6GABRR1LMNATET2
Malic Acid SCHEMBL856 0.75
Malic Acid SCHEMBL14125844 0.75 SMN1; SMN2 (1.00) SMN1; SMN2SLC22A6GABRR1LMNATDP1
Malic Acid SCHEMBL98496 0.75
Malic Acid SCHEMBL256122 0.75
Malic Acid SCHEMBL89131 0.75 SMN1; SMN2 (1.00) SMN1; SMN2SLC22A6GABRR1LMNATDP1
Malic Acid SCHEMBL31673489 0.75

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20200231527-A1 SYNTHESIS OF ORGANIC ACIDS FROM ALPHA-KETO ACIDS FURMAN UNIVERSITY 2020-07-23 US claimed
EP-0884390-B1 Method for producing an optically active compound KYOWA HAKKO KOGYO KK (JP) 2006-05-10 EP claimed
CN-119330823-A Long carbon chain hydroxyl-containing branched dicarboxylic acid, and preparation method and application thereof 华中师范大学 2025-01-21 CN disclosed
US-20230190910-A1 SCAFFOLDED HIV-1 VACCINE IMMUNOGENS SCRIPPS RESEARCH INST (US) 2023-06-22 US disclosed
US-11505519-B2 Synthesis of organic acids from α-keto acids FURMAN UNIVERSITY (US) 2022-11-22 US disclosed
US-11452771-B2 Scaffolded HIV-1 Env GP140 trimer immunogen THE SCRIPPS RESEARCH INSTITUTE (US) 2022-09-27 US disclosed
EP-3911624-A1 SYNTHESIS OF ORGANIC ACIDS FROM ALPHA-KETO ACIDS Furman University (US) 2021-11-24 EP disclosed
US-20200231527-A1 SYNTHESIS OF ORGANIC ACIDS FROM ALPHA-KETO ACIDS FURMAN UNIVERSITY 2020-07-23 US disclosed
WO-2020150568-A1 SYNTHESIS OF ORGANIC ACIDS FROM ALPHA-KETO ACIDS FURMAN UNIVERSITY (US) 2020-07-23 WO disclosed
US-10711043-B2 Compositions and vaccines comprising vesicles and methods of using the same UNIVERSITY OF MARYLAND, COLLEGE PARK (US) 2020-07-14 US disclosed
US-20190016761-A1 Compositions and Vaccines Comprising Vesicles and Methods of Using the Same UNIVERSITY OF MARYLAND, COLLEGE PARK 2019-01-17 US disclosed
EP-1877567-A2 POLYPEPTIDES AND BIOSYNTHETIC PATHWAYS FOR THE PRODUCTION OF MONATIN AND ITS PRECURSORS CARGILL, INCORPORATED (US) 2008-01-16 EP disclosed
WO-2007103989-A9 ALDOLASES, NUCLEIC ACIDS ENCODING THEM AND METHODS FOR MAKING AND USING THEM VERENIUM CORP (US) 2007-11-29 WO disclosed
WO-2007103389-A9 ALDOLASES, NUCLEIC ACIDS ENCODING THEM AND METHODS FOR MAKING AND USING THEM CARGILL INC (US) 2007-11-01 WO disclosed
WO-2007103389-A2 ALDOLASES, NUCLEIC ACIDS ENCODING THEM AND METHODS FOR MAKING AND USING THEM CARGILL, INCORPORATED (US) 2007-09-13 WO disclosed
WO-2007103989-A2 ALDOLASES, NUCLEIC ACIDS ENCODING THEM AND METHODS FOR MAKING AND USING THEM VERENIUM CORPORATION (US) 2007-09-13 WO disclosed
WO-2006116487-A2 POLYPEPTIDES AND BIOSYNTHETIC PATHWAYS FOR THE PRODUCTION OF MONATIN AND ITS PRECURSORS CARGILL, INCORPORATED (US) 2006-11-02 WO disclosed
EP-0692539-B1 Process for producing an optically active gamma-hydroxy-L-glutamic acid KYOWA HAKKO KOGYO KK (JP) 1999-09-22 EP disclosed
US-5643769-A Process for producing an optically active γ-hydroxy-L-glutamic acid KYOWA HAKKO KOGYO CO., LTD. (JP) 1997-07-01 US disclosed
EP-0692539-A2 Process for producing an optically active gamma-hydroxy-L-glutamic acid KYOWA HAKKO KOGYO CO., LTD. (JP) 1996-01-17 EP 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 (2 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-20200231527-A1 SYNTHESIS OF ORGANIC ACIDS FROM ALPHA-KETO ACIDS HOGA1, BCKDK, PCCA SMN1; SMN2 4397/4885SLC22A6 1831/4885GABRR1 1215/4885
US-11505519-B2 Synthesis of organic acids from α-keto acids HOGA1, BCKDK, KHK SMN1; SMN2 4489/4885SLC22A6 1680/4885GABRR1 1161/4885

“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.