Malonic Acid

Malonic Acid

SCHEMBL8847214

O=C(O)CC(=O)O.O=[N+]([O-])c1ccc(C[Mg+2])cc1.O=[N+]([O-])c1ccc(C[Mg+2])cc1

nearest known ligand 0.51

Full drug profile on Sugi Atlas →

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ CYP2C19 P33261 3/20 0.51
▸ ALDH1A1 P00352 1/20 0.51
▸ TSHR P16473 1/20 0.50
▸ CYP1A2 P05177 2/20 0.49
▸ LOXL2 Q9Y4K0 1/20 0.48
▸ TDP1 Q9NUW8 1/20 0.48
▸ PTPRF P10586 1/20 0.47
▸ PTPN2 P17706 1/20 0.47
▸ PTPN1 P18031 1/20 0.47
▸ PTPN11 Q06124 1/20 0.47
▸ MEN1 O00255 2/20 0.47
▸ KMT2A Q03164 2/20 0.47
▸ CES1 P23141 2/20 0.46
▸ MAPT P10636 1/20 0.45
▸ CA2 P00918 1/20 0.44
▸ IDO1 P14902 1/20 0.44
▸ CES2 O00748 1/20 0.44
▸ SRD5A2 P31213 1/20 0.44

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
Paranitrobenzyl Alcohol SCHEMBL5689999 0.84 TSHR (0.56) CYP2C19ALDH1A1TSHRCYP1A2LOXL2
SCHEMBL30643815 0.77 CYP2C19 (0.64) CYP2C19ALDH1A1TSHRCYP1A2LOXL2
SCHEMBL76204 0.77 CYP2C19 (0.64) CYP2C19ALDH1A1TSHRCYP1A2LOXL2
Malonic Acid SCHEMBL8982152 0.77 ALDH1A1 (0.54) ALDH1A1MAPTIDO1
SCHEMBL10999840 0.76 MMP12 (0.58) CYP2C19ALDH1A1TSHRCYP1A2LOXL2
SCHEMBL1369963 0.76 CYP2C19 (0.62) CYP2C19ALDH1A1TSHRCYP1A2LOXL2
Hydrochloric Acid SCHEMBL2527458 0.76 CYP2C19 (0.62) CYP2C19ALDH1A1TSHRCYP1A2LOXL2
SCHEMBL1369959 0.76 CYP2C19 (0.62) CYP2C19ALDH1A1TSHRCYP1A2LOXL2
SCHEMBL27861234 0.76 CYP2C19 (0.62) CYP2C19ALDH1A1TSHRCYP1A2LOXL2
SCHEMBL1554845 0.75 ALDH1A1 (0.55) ALDH1A1MAPTIDO1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5700780-A OLIGOPEPTIDE VIRICIDES; RIBONUCLEOTIDE REDUCTASE ENZYME INHIBITOR BOEHRINGER INGELHEIM (CANADA), LTD. (CA) 1997-12-23 — — US disclosed
EP-0493770-B1 Antiherpes compositions BOEHRINGER INGELHEIM CA LTD (CA) 1997-08-06 — — EP disclosed
EP-0493767-B1 Synergistic combination for treating herpes infections BIO MEGA BOEHRINGER INGELHEIM (CA) 1997-03-19 — — EP disclosed
US-5552384-A Antiherpes compositions and method of use BIO-MEGA BOEHRINGER INGELHEIM RESEARCH INC. (CA) 1996-09-03 — — US disclosed
EP-0411332-B1 Antiviral peptides having a 2-oxoalkyl amino acid side chain BIO MEGA BOEHRINGER INGELHEIM (CA) 1995-12-06 — — EP disclosed
US-5380727-A Antiviral nucleoside analog and a ribonucleotide reductase inhibiting peptide derivative BIO-MEGA, INC. (CA) 1995-01-10 — — US disclosed
EP-0326640-B1 (1R,5S,6S)-2-SUBSTITUTED THIO-6 (R)-1-HYDROXYETHYL -1-METHYL-CARBAPENEM - CARBOXYLIC ACID DERIVATIVES LEDERLE (JAPAN) LTD. (JP) 1993-04-28 — — EP disclosed
EP-0493770-A2 Antiherpes compositions BIO-MEGA/BOEHRINGER INGELHEIM RESEARCH INC. (CA) 1992-07-08 — — EP disclosed
EP-0493767-A2 Synergistic combination for treating herpes infections BIO-MEGA/BOEHRINGER INGELHEIM RESEARCH INC. (CA) 1992-07-08 — — EP disclosed
US-4990613-A Bactericides LEDERLE (JAPAN), LTD. (JP) 1991-02-05 — — US disclosed
EP-0289801-B1 (1R,5S,6S)-2-(substituted thio)-6-[(R)-1-hydroxy-ethyl]-1-methyl-carbapenem-3-carboxylic-acid derivatives LEDERLE (JAPAN) LTD. (JP) 1990-11-07 — — EP disclosed
US-4925836-A NONTOXIC, SIDE EFFECT REDUCTION LEDERLE (JAPAN), LTD. (JP) 1990-05-15 — — US disclosed
US-4925935-A BACTERICIDES LEDERLE (JAPAN), LTD. (JP) 1990-05-15 — — US disclosed
US-4866171-A THIENAMYCIN ANTIBIOTIC LEDERLE (JAPAN), LTD. (JP) 1989-09-12 — — US disclosed
EP-0326640-A1 (1R,5S,6S)-2-substituted thio-6 (R)-1-hydroxyethyl -1-methyl-carbapenem - carboxylic acid derivatives LEDERLE (JAPAN) LTD. (JP) 1989-08-09 — — EP disclosed
EP-0289801-A1 (1R,5S,6S)-2-(substituted thio)-6-[(R)-1-hydroxy-ethyl]-1-methyl-carbapenem-3-carboxylic-acid derivatives LEDERLE (JAPAN) LTD. (JP) 1988-11-09 — — EP disclosed
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