L-Lactic Acid

L-Lactic Acid

SCHEMBL2580452

CC(O)C(=O)[O-].CC(O)C(=O)[O-].O=S(=O)(O)O.[Ca+2]

nearest known ligand 0.71

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 13)

geneUniProtsupporting neighboursconfidence
TP53 P04637 2/20 0.40
CA5A P35218 1/20 0.35
CA5B Q9Y2D0 1/20 0.35
CA4 P22748 2/20 0.32
CA2 P00918 1/20 0.32
CA1 P00915 5/20 0.32
TSHR P16473 2/20 0.31
CYP3A4 P08684 1/20 0.31
NFKB1 P19838 1/20 0.31
NPSR1 Q6W5P4 1/20 0.31
MEN1 O00255 1/20 0.30
ALDH1A1 P00352 1/20 0.30
KMT2A Q03164 1/20 0.30

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 SCHEMBL27674550 1.00 TP53 (0.40) TP53CA5ACA5BCA4CA2
L-Lactic Acid SCHEMBL28286518 0.94 TP53 (0.40) TP53CA5ACA5BCA4CA2
L-Lactic Acid SCHEMBL6394826 0.88 TP53 (0.40) TP53CA4CA2CA1TSHR
L-Lactic Acid SCHEMBL3446641 0.88 TP53 (0.40) TP53CA4CA2CA1TSHR
L-Lactic Acid SCHEMBL2419423 0.87 TP53 (0.50) TP53CA4CA2CA1TSHR
L-Lactic Acid SCHEMBL29683322 0.87 TP53 (0.50) TP53CA4CA2CA1TSHR
L-Lactic Acid SCHEMBL1532627 0.87 TP53 (0.50) TP53CA4CA2CA1TSHR
L-Lactic Acid SCHEMBL29351424 0.87 TP53 (0.50) TP53CA4CA2CA1TSHR
L-Lactic Acid SCHEMBL4319 0.87 TP53 (0.50) TP53CA4CA2CA1TSHR
L-Lactic Acid SCHEMBL4648043 0.87 TP53 (0.50) TP53CA4CA2CA1TSHR

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108129290-A A kind of method of sulfate radical in removal lactic acid 武汉三江航天固德生物科技有限公司 2018-06-08 CN disclosed
CN-102864105-B Method for producing L-lactic acid and Exiguobacterium aurantiacum special for method CHINESE ACAD INST MICROBIOLOGY 2013-10-23 CN disclosed
CN-103194402-A L-lactic acid production method and special Bacillus sp. therefor CHINESE ACAD INST MICROBIOLOGY 2013-07-10 CN disclosed
CN-102864105-A Method for producing L-lactic acid and Exiguobacterium aurantiacum special for method CHINESE ACAD INST MICROBIOLOGY 2013-01-09 CN disclosed
US-20120112127-A1 RECOVERY OF ORGANIC ACIDS ZEACHEM, INC. (US) 2012-05-10 US disclosed
US-8048655-B2 Recovery of organic acids ZEACHEM, INC. (US) 2011-11-01 US disclosed
CN-102050723-A Method for producing sodium lactate CHINA PETROLEUM & CHEMICAL 2011-05-11 CN disclosed
US-20100187472-A1 RECOVERY OF ORGANIC ACIDS ZEACHEM, INC. (US) 2010-07-29 US disclosed
US-7601865-B2 Introducing tertiary amine and CO2 to dilute salt solution to form acid/amine complex and insoluble carbonate salt, introducing water immiscible solvent to dilute salt solution to form reaction phase, continuously drying reaction phase and forming product ZEACHEM, INC. (US) 2009-10-13 US disclosed
US-20050256337-A1 Introducing tertiary amine and CO2 to dilute salt solution to form acid/amine complex and insoluble carbonate salt, introducing water immiscible solvent to dilute salt solution to form reaction phase, continuously drying reaction phase and forming product ZEACHEM INC. (US) 2005-11-17 US disclosed