Maleic Acid

Maleic Acid

SCHEMBL5334785

O=C(O)/C=C\C(=O)O.O=C1NC(=O)C2(O)CCCCC12

nearest known ligand 0.34

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2BTKCACNA1CCACNA1DCACNA1FCACNA1SCCR5CPT1BCPT2DPP4DRD1DRD2EGFRERBB2ERBB4HRH1HRH3HTR1AHTR2AHTR2BHTR2CHTR4JAK1JAK2JAK3MPLMTORPPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PPARGSLC6A2SLC6A3SLC6A4SMOTYK2pol

The experimentally established mechanism targets of Maleic 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
HTT P42858 3/20 0.34
SMN1; SMN2 Q16637 2/20 0.34
NPC1 O15118 1/20 0.34
GAA P10253 1/20 0.34
LMNA P02545 2/20 0.33
TSHR P16473 1/20 0.33
MEN1 O00255 1/20 0.31
MITF O75030 1/20 0.31
TP53 P04637 1/20 0.31
CYP3A4 P08684 1/20 0.31
MAPT P10636 1/20 0.31
ALOX15 P16050 1/20 0.31
KMT2A Q03164 1/20 0.31
NPSR1 Q6W5P4 1/20 0.31
NLRP1 Q9C000 1/20 0.31
GPR55 Q9Y2T6 1/20 0.31
OPRM1 P35372 3/20 0.30
OPRL1 P41146 3/20 0.30
SLC6A9 P48067 3/20 0.30
SLC6A5 Q9Y345 3/20 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
SCHEMBL5031774 0.90 LMNA (0.34) HTTLMNATSHRCYP3A4OPRM1
SCHEMBL476025 0.90 LMNA (0.34) HTTLMNATSHRCYP3A4OPRM1
Hydrochloric Acid SCHEMBL5234106 0.88 LMNA (0.33) HTTLMNATSHROPRM1OPRL1
Cadaverine Tartrate SCHEMBL5328580 0.84 TSHR (0.33) HTTSMN1; SMN2LMNATSHRMAPT
Maleic Acid SCHEMBL5326719 0.74 HTT (0.31) HTTSMN1; SMN2NPC1GAAPOLB
Maleic Acid SCHEMBL5326717 0.74 HTT (0.32) HTTSMN1; SMN2NPC1GAALMNA
Fumaric Acid SCHEMBL5326723 0.74 HTT (0.32) HTTSMN1; SMN2NPC1GAALMNA
SCHEMBL6901500 0.65 HSD11B1 (0.31)
SCHEMBL2106696 0.65 CCR2 (0.33) HTT
SCHEMBL2011171 0.65 HSD11B1 (0.31)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2007010504-A2 ACID ADDITION SALTS OF ISOINDOLES ACTING AS ADRENERGIC RECEPTOR ANTAGONISTS RANBAXY LABORATORIES LIMITED (IN) 2007-01-25 WO claimed