Lactic Acid

Lactic Acid

SCHEMBL232168

CC(O)C(=O)O.O=S(=O)(O)c1ccccc1

nearest known ligand 0.67

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

BTKCACNA1CCACNA1DCACNA1FCACNA1SCACNA2D1CACNA2D2DRD2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQHRH1HTR2AP2RY12

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
TSHR P16473 1/20 0.67
SMN1; SMN2 Q16637 1/20 0.67
POLB P06746 2/20 0.47
CYP2D6 P10635 1/20 0.47
TP53 P04637 1/20 0.46
LMNA P02545 4/20 0.45
MAPK1 P28482 1/20 0.45
SRC P12931 1/20 0.44
ADAMTS4 O75173 1/20 0.42
ALDH1A1 P00352 2/20 0.42
TDP1 Q9NUW8 2/20 0.42
KDM4E B2RXH2 1/20 0.42
GMNN O75496 1/20 0.42
MAPT P10636 1/20 0.42
HPGD P15428 1/20 0.42
PMP22 Q01453 1/20 0.42
KMT2A Q03164 1/20 0.42
NPSR1 Q6W5P4 1/20 0.42
CYP2C19 P33261 1/20 0.41
CASR P41180 1/20 0.41

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 SCHEMBL28201828 0.98 TSHR (0.64) TSHRSMN1; SMN2POLBCYP2D6TP53
Isopropyl Alcohol SCHEMBL5735328 0.89 TSHR (0.76) TSHRSMN1; SMN2POLBCYP2D6LMNA
SCHEMBL16046756 0.87 TSHR (0.73) TSHRSMN1; SMN2POLBCYP2D6LMNA
Alanine SCHEMBL10626231 0.86 TSHR (0.64) TSHRSMN1; SMN2POLBCYP2D6MAPK1
Alanine SCHEMBL10627958 0.86 TSHR (0.64) TSHRSMN1; SMN2POLBCYP2D6MAPK1
SCHEMBL28902110 0.85 TSHR (0.70) TSHRSMN1; SMN2POLBCYP2D6LMNA
Cadaverine Tartrate SCHEMBL231944 0.85 TSHR (0.70) TSHRSMN1; SMN2POLBCYP2D6LMNA
SCHEMBL5875401 0.85 TSHR (0.70) TSHRSMN1; SMN2POLBCYP2D6LMNA
Lactic Acid SCHEMBL2447119 0.84 CYP2D6 (0.49) TSHRSMN1; SMN2CYP2D6TP53LMNA
SCHEMBL16045501 0.83 TSHR (0.67) TSHRSMN1; SMN2POLBCYP2D6LMNA

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
JP-53063343-A None JP disclosed
CN-102070587-B One kettle way prepares the method for Simvastatin SUNSHINE LAKE PHARMA CO.,LTD. (CN) 2015-10-14 CN disclosed
US-8710071-B2 Compounds, compositions and methods for reducing lipid levels CVI PHARMACEUTICALS LIMITED (KY) 2014-04-29 US disclosed
EP-2464644-A1 SOLID ORAL FORMULATIONS AND CRYSTALLINE FORMS OF AN INHIBITOR OF APOPTOSIS PROTEIN Novartis AG (CH) 2012-06-20 EP disclosed
US-20120004223-A1 COMPOUNDS, COMPOSITIONS AND METHODS FOR REDUCING LIPID LEVELS CVI PHARMACEUTICALS LIMITED (KY) 2012-01-05 US disclosed
WO-2011018474-A1 SOLID ORAL FORMULATIONS AND CRYSTALLINE FORMS OF AN INHIBITOR OF APOPTOSIS PROTEIN NOVARTIS AG (CH) 2011-02-17 WO disclosed
JP-S5363343-A PREPARATION OF ALPHA-PHENYLPROPIONIC ACID DERIVS. MITSUI TOATSU CHEM INC 1978-06-06 JP 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 (1 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-20120004223-A1 COMPOUNDS, COMPOSITIONS AND METHODS FOR REDUCING LIPID LEVELS LIPC, LDLR, PCSK9 TSHR 1637/4885SMN1; SMN2 4854/4885POLB 3099/4885

“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.