Lactic Acid

Lactic Acid

SCHEMBL8622247

CC(O)C(=O)O.O=C(O)Nc1ccccc1

nearest known ligand 0.59

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 20)

geneUniProtsupporting neighboursconfidence
HDAC3 known ✓ O15379 2/20 0.56
HDAC4 known ✓ P56524 2/20 0.56
HDAC1 known ✓ Q13547 2/20 0.56
HDAC7 known ✓ Q8WUI4 2/20 0.56
HDAC2 known ✓ Q92769 2/20 0.56
HDAC10 known ✓ Q969S8 2/20 0.56
HDAC11 known ✓ Q96DB2 2/20 0.56
HDAC8 known ✓ Q9BY41 2/20 0.56
HDAC6 known ✓ Q9UBN7 2/20 0.56
HDAC9 known ✓ Q9UKV0 2/20 0.56
HDAC5 known ✓ Q9UQL6 2/20 0.56
MAPT P10636 5/20 0.56
MEN1 O00255 3/20 0.56
KMT2A Q03164 3/20 0.56
ALDH1A1 P00352 3/20 0.56
RXFP1 Q9HBX9 1/20 0.56
HSD17B10 Q99714 2/20 0.54
NAPRT Q6XQN6 1/20 0.54
SMN1; SMN2 Q16637 3/20 0.52
TP53 P04637 1/20 0.52

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 SCHEMBL7787988 1.00 MAPT (0.56) MAPTMEN1KMT2AALDH1A1RXFP1
Isopropyl Alcohol SCHEMBL11779348 0.91 HSD17B10 (0.58) MAPTMEN1KMT2AALDH1A1RXFP1
Diphenylamine SCHEMBL21145224 0.85 MAPT (0.62) MAPTMEN1KMT2AALDH1A1RXFP1
Benzene SCHEMBL28162617 0.84 EPHX2 (0.70) MAPTKMT2AALDH1A1HSD17B10NAPRT
SCHEMBL7634 0.84 EPHX2 (0.70) MAPTKMT2AALDH1A1HSD17B10NAPRT
Dimethylamine SCHEMBL8779747 0.82 NAPRT (0.62) MAPTKMT2AHSD17B10NAPRTSMN1; SMN2
Acetic Acid SCHEMBL6421164 0.82 NAPRT (0.70) MAPTMEN1KMT2AALDH1A1HSD17B10
Iodide SCHEMBL5706290 0.82 EPHX2 (0.67) MAPTKMT2AALDH1A1HSD17B10NAPRT
SCHEMBL11353365 0.82 EPHX2 (0.67) MAPTKMT2AALDH1A1HSD17B10NAPRT
Bromide SCHEMBL5706299 0.82 EPHX2 (0.67) MAPTKMT2AALDH1A1HSD17B10NAPRT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1128785-C Method for producing optically active 1-phenylethylamines BAYER AG (DE) 2003-11-26 CN claimed
CN-1222140-A Process for preparing optically active 1-phenyl-ethylamines BAYER AG (DE) 1999-07-07 CN claimed
JP-10045686-A None JP disclosed
CN-1128785-C Method for producing optically active 1-phenylethylamines BAYER AG (DE) 2003-11-26 CN disclosed
CN-1226228-A Process for preparing preparing racemic phenethylamines BAYER AG (DE) 1999-08-18 CN disclosed
CN-1222140-A Process for preparing optically active 1-phenyl-ethylamines BAYER AG (DE) 1999-07-07 CN disclosed
JP-H1045686-A PRODUCTION OF OPTICALLY ACTIVE 1-PHENYL-ETHYLAMINES BAYER AG 1998-02-17 JP disclosed