Lactic Acid

Lactic Acid

SCHEMBL424598

CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.CC(O)C(=O)O.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO.O=C(O)CO

nearest known ligand 0.69

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CHRM1DRD2DRD3DRD4HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR2APDE3ASIGMAR1

The experimentally established mechanism targets of 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 13)

geneUniProtsupporting neighboursconfidence
TP53 P04637 1/20 0.69
OR51E2 Q9H255 1/20 0.43
CYP1A2 P05177 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.41
CYP2C9 P11712 1/20 0.40
TSHR P16473 1/20 0.40
SLC22A6 Q4U2R8 1/20 0.38
TET2 Q6N021 3/20 0.38
KDM4A O75164 2/20 0.38
KDM4C Q9H3R0 2/20 0.38
KDM2A Q9Y2K7 2/20 0.38
TET3 O43151 1/20 0.38
FFAR3 O14843 1/20 0.37

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
Lactic Acid SCHEMBL13505613 1.00 TP53 (0.69) TP53OR51E2CYP1A2SMN1; SMN2CYP2C9
Lactic Acid SCHEMBL7026852 1.00 TP53 (0.69) TP53OR51E2CYP1A2SMN1; SMN2CYP2C9
Lactic Acid SCHEMBL4263083 1.00 TP53 (0.69) TP53OR51E2CYP1A2SMN1; SMN2CYP2C9
Lactic Acid SCHEMBL419437 1.00 TP53 (0.69) TP53OR51E2CYP1A2SMN1; SMN2CYP2C9
Lactic Acid SCHEMBL41708 1.00 TP53 (0.69) TP53OR51E2CYP1A2SMN1; SMN2CYP2C9
Lactic Acid SCHEMBL4261279 1.00 TP53 (0.69) TP53OR51E2CYP1A2SMN1; SMN2CYP2C9
Lactic Acid SCHEMBL3845012 1.00 TP53 (0.69) TP53OR51E2CYP1A2SMN1; SMN2CYP2C9
Lactic Acid SCHEMBL5269783 1.00 TP53 (0.69) TP53OR51E2CYP1A2SMN1; SMN2CYP2C9
Lactic Acid SCHEMBL2286708 1.00 TP53 (0.69) TP53OR51E2CYP1A2SMN1; SMN2CYP2C9
Lactic Acid SCHEMBL15008846 0.97 TP53 (0.65) TP53OR51E2CYP1A2SMN1; SMN2CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118217226-A Photo-thermal composite hydrogel with adjustable slow release performance and preparation method thereof 西北有色金属研究院 2024-06-21 CN claimed
CN-118217226-A Photo-thermal composite hydrogel with adjustable slow release performance and preparation method thereof 西北有色金属研究院 2024-06-21 CN disclosed
US-10632079-B2 Microspheres having core/shell structure OTSUKA PHARMACEUTICALS CO., LTD. (JP) 2020-04-28 US disclosed
EP-3479839-A1 METHODS AND COMPOSITIONS FOR PREVENTING OR TREATING OPTHALMIC CONDITIONS Stealth Peptides International, Inc. (MC) 2019-05-08 EP disclosed
US-20180296630-A1 METHODS AND COMPOSITIONS FOR PREVENTING OR TREATING OPHTHALMIC CONDITIONS STEALTH BIOTHERAPEUTICS INC. 2018-10-18 US disclosed
EP-3281634-A1 METHOD AND COMPOSITIONS FOR PREVENTING OR TREATING OPHTHALMIC CONDITIONS Stealth Peptides International, Inc. (MC) 2018-02-14 EP disclosed
US-20160361377-A1 METHODS AND COMPOSITIONS FOR PREVENTING OR TREATING OPHTHALMIC CONDITIONS STEALTH BIOTHERAPEUTICS INC. 2016-12-15 US disclosed
EP-3078384-A1 METHODS AND COMPOSITIONS FOR PREVENTING OR TREATING OPHTHALMIC CONDITIONS Stealth Peptides International, Inc. (MC) 2016-10-12 EP disclosed
EP-2351574-B1 PROMOTER FOR REGENERATION OF TENDON-BONE JUNCTION TISSUE OR LIGAMENT-BONE JUNCTION TISSUE KRINGLE PHARMA INC (JP) 2016-08-24 EP disclosed
EP-1765295-B2 A PROCESS FOR PRODUCING A SUSTAINED-RELEASE MICROCAPSULE TAKEDA PHARMACEUTICAL (JP) 2015-09-09 EP disclosed
EP-0647449-A1 Sustained-release preparation of anti-endothelin substance Takeda Chemical Industries, Ltd. (JP) 1995-04-12 EP disclosed
EP-0601799-A1 Sustained-release preparation TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1994-06-15 EP disclosed
EP-0582459-A2 Production of microcapsules of water-soluble drugs TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1994-02-09 EP disclosed
US-5202352-A Antitumor agents TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1993-04-13 US disclosed
EP-0535937-A1 Prolonged release microparticle preparation and production of the same TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1993-04-07 EP disclosed
EP-0256726-B1 ENCAPSULATION OF TRH OR ITS ANALOG Takeda Chemical Industries, Ltd. (JP) 1992-10-07 EP disclosed
EP-0470569-A1 Intravascular embolizing agent containing angiogenesis inhibiting substance Takeda Chemical Industries, Ltd. (JP) 1992-02-12 EP disclosed
EP-0429245-A2 A therapeutic agent for central nervous diseases Takeda Chemical Industries, Ltd. (JP) 1991-05-29 EP disclosed
EP-0256726-A2 Encapsulation of TRH or its analog Takeda Chemical Industries, Ltd. (JP) 1988-02-24 EP disclosed
US-4612364-A EVAPORATION OF HALOGEN SOLVENT TAKEDA CHEMICAL INDUSTRIES (JP) 1986-09-16 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-20160361377-A1 METHODS AND COMPOSITIONS FOR PREVENTING OR TREATING OPHTHALMIC CONDITIONS ADM2, ARG1, IAPP TP53 2307/4885OR51E2 3094/4885CYP1A2 4874/4885
US-20180296630-A1 METHODS AND COMPOSITIONS FOR PREVENTING OR TREATING OPHTHALMIC CONDITIONS ADM2, ARG1, IAPP TP53 2307/4885OR51E2 3094/4885CYP1A2 4874/4885

“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.