L-Lactic Acid

L-Lactic Acid

SCHEMBL668885

CC(O)C(=O)[O-].CC(O)C(=O)[O-].CC(O)C(=O)[O-].CC(O)C(=O)[O-].[C+4]

nearest known ligand 0.92

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CHRM1DRD2DRD3DRD4HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR2APDE3ASIGMAR1SLC9A3

The experimentally established mechanism targets of L-Lactic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
▸ TP53 P04637 1/20 0.50
▸ CA1 P00915 5/20 0.42
▸ CA4 P22748 3/20 0.38
▸ CA2 P00918 1/20 0.38
▸ CYP3A4 P08684 1/20 0.36
▸ TSHR P16473 1/20 0.36
▸ NFKB1 P19838 1/20 0.36
▸ NPSR1 Q6W5P4 1/20 0.36
▸ ALDH1A1 P00352 1/20 0.36
▸ LMNA P02545 1/20 0.36

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
L-Lactic Acid SCHEMBL2574910 1.00 — —
L-Lactic Acid SCHEMBL11294028 0.96 TP53 (0.47) TP53CA1CA4CA2CYP3A4
L-Lactic Acid SCHEMBL3759604 0.92 TP53 (0.50) TP53CA1CA4CA2CYP3A4
L-Lactic Acid SCHEMBL21815670 0.92 TP53 (0.50) TP53CA1CA4CA2CYP3A4
L-Lactic Acid SCHEMBL6709684 0.92 — —
L-Lactic Acid SCHEMBL19180003 0.92 TP53 (0.50) TP53CA1CA4CA2CYP3A4
L-Lactic Acid SCHEMBL116857 0.92 TP53 (0.50) TP53CA1CA4CA2CYP3A4
L-Lactic Acid SCHEMBL22341771 0.92 TP53 (0.50) TP53CA1CA4CA2CYP3A4
L-Lactic Acid SCHEMBL3767825 0.92 TP53 (0.50) TP53CA1CA4CA2CYP3A4
L-Lactic Acid SCHEMBL186171 0.92 — —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240285683-A1 Compositions And Methods For Enhancing Immunotherapy THE TRUSTEES OF PRINCETON UNIVERSITY 2024-08-29 — — US disclosed
US-20230286895-A1 METHODS FOR PRODUCING ALKYL HYDROXYALKANOATES CARGILL, INCORPORATED (US) 2023-09-14 — — US disclosed
US-11691941-B2 Methods for producing alkyl hydroxyalkanoates CARGILL, INCORPORATED (US) 2023-07-04 — — US disclosed
WO-2023081775-A1 COMBINATION INHIBITORS FOR TREATING FIBROSIS MEMORIAL SLOAN-KETTERING CANCER CENTER (US) 2023-05-11 — — WO disclosed
CN-115636526-A Organic pollutant migration and conversion method based on Fe redox enhancement 中国科学院南京土壤研究所 2023-01-24 — — CN disclosed
US-11332428-B2 Methods for producing alkyl hydroxy alkanoates CARGILL, INCORPORATED (US) 2022-05-17 — — US disclosed
US-11332429-B2 Methods for producing alkyl hydroxyalkanoates CARGILL, INCORPORATED (US) 2022-05-17 — — US disclosed
US-20210187023-A1 Compositions And Methods For Enhancing Immunotherapy THE TRUSTEES OF PRINCETON UNIVERSITY 2021-06-24 — — US disclosed
US-20200331839-A1 METHODS FOR PRODUCING ALKYL HYDROXYALKANOATES CARGILL, INCORPORATED (US) 2020-10-22 — — US disclosed
US-10710955-B2 Methods for producing alkyl hydroxyalkanoates CARGILL, INCORPORATED (US) 2020-07-14 — — US disclosed
US-20100062483-A1 PRODUCTION OF BIO-BASED MATERIALS USING PHOTOBIOREACTORS WITH BINARY CULTURES BATTELLE MEMORIAL INSTITUTE (US) 2010-03-11 — — US disclosed
US-20100059436-A1 SYSTEMS AND METHODS FOR MICROBIAL REDUCTIVE DECHLORINATION OF ENVIRONMENTAL CONTAMINANTS UNIVERSITY OF MASSACHUSETTS (US) 2010-03-11 — — US disclosed
EP-1942092-A1 Preparation of propylene glycol by hydrogenating lactate or lactic acid Battelle Memorial Institute (US) 2008-07-09 — — EP disclosed
CN-101074242-A Cells accumulation for sphosphonate analogs of HIV protease inhibitor compound and the same compound GILEAD SCIENCES INC (US) 2007-11-21 — — CN disclosed
CN-1313472-C Cellular Accumulation of Phosphonate Analogs of HIV Protease Inhibitor Compounds and Such Compounds GILEAD SCIENCES INC (US) 2007-05-02 — — CN disclosed
CN-1649885-A Cellular Accumulation of Phosphonate Analogs of HIV Protease Inhibitor Compounds and Such Compounds GILEAD SCIENCES INC (US) 2005-08-03 — — CN disclosed
WO-1999021544-A1 NOVEL PHARMACEUTICAL ALPHA-KETO CARBOXYLIC ACID COMPOSITIONS, METHOD OF MAKING AND USE THEREOF UNITED STATES GOVERNMENT, AS REPRESENTED BY THE SECRETARY OF THE ARMY (US) 1999-05-06 — — WO disclosed
US-5714515-A Pharmaceutical alpha-keto carboxylic acid compositions, method of making and use thereof THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE ARMY (US) 1998-02-03 — — US disclosed
WO-1997041848-A1 PHARMACEUTICAL COMPOSITIONS CONTAINING ALPHA-KETO CARBOXYLATES THE GOVERNMENT OF THE UNITED STATES, REPRESENTED BY THE SECRETARY OF THE ARMY (US) 1997-11-13 — — WO disclosed
US-5536751-A PHOSPHORYLATION POTENTIAL THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE ARMY (US) 1996-07-16 — — 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 (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-20240285683-A1 Compositions And Methods For Enhancing Immunotherapy RNASE1, DERA, SLC2A1 TP53 82/4885CA1 347/4885CA4 397/4885
US-20210187023-A1 Compositions And Methods For Enhancing Immunotherapy RNASE1, DERA, SLC2A1 TP53 82/4885CA1 347/4885CA4 397/4885

“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.

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