Maleic Acid

Maleic Acid

SCHEMBL7175246

C=C(CC)C(=O)OC(=O)C(=C)C(C)C=Cc1ccccc1.O=C(O)/C=C\C(=O)O

nearest known ligand 0.41

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
HCAR2 Q8TDS4 2/20 0.41
HDAC3 O15379 1/20 0.41
TNKS O95271 1/20 0.41
HDAC4 P56524 1/20 0.41
HDAC1 Q13547 1/20 0.41
HDAC7 Q8WUI4 1/20 0.41
HDAC2 Q92769 1/20 0.41
HDAC10 Q969S8 1/20 0.41
HDAC11 Q96DB2 1/20 0.41
HDAC8 Q9BY41 1/20 0.41
TNKS2 Q9H2K2 1/20 0.41
HDAC6 Q9UBN7 1/20 0.41
HDAC9 Q9UKV0 1/20 0.41
HDAC5 Q9UQL6 1/20 0.41
ESR1 P03372 7/20 0.40
ESR2 Q92731 3/20 0.40
PGR P06401 2/20 0.40
ALDH1A1 P00352 2/20 0.38
NPC1 O15118 1/20 0.37
L3MBTL1 Q9Y468 1/20 0.37

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
Maleic Acid SCHEMBL7173176 0.81 ESR1 (0.36) HCAR2ESR1ESR2PGRALDH1A1
Maleic Acid SCHEMBL4001893 0.78 ALDH1A1 (0.41) HCAR2HDAC3TNKSHDAC4HDAC1
SCHEMBL27890646 0.76 LMNA (0.50) HCAR2HDAC3TNKSHDAC4HDAC1
SCHEMBL28613781 0.76 LMNA (0.50) HCAR2HDAC3TNKSHDAC4HDAC1
Maleic Acid SCHEMBL3692041 0.74 HCAR2 (0.45) HCAR2ALDH1A1L3MBTL1
SCHEMBL179701 0.73 CYP1A2 (0.49) HCAR2HDAC3TNKSHDAC4HDAC1
SCHEMBL5162573 0.72 TSHR (0.46) ALDH1A1NPC1KDM4ESMN1; SMN2TDP1
SCHEMBL7998352 0.72 LMNA (0.49) HCAR2HDAC3TNKSHDAC4HDAC1
SCHEMBL10584305 0.72 LMNA (0.49) HCAR2HDAC3TNKSHDAC4HDAC1
Juarezic Acid SCHEMBL6858341 0.72 HDAC3 (0.49) HCAR2HDAC3TNKSHDAC4HDAC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0902810-B1 THERMOPLASTIC MOULDED MATERIALS BASED ON POLYCARBONATES AND STYRENE/ACRYLONITRILE POLYMERS WHICH CONTAIN COPOLYMERS BASED ON ALKYL(METH)ACRYLATE TO IMPROVE THEIR PROPERTIES BASF AG (DE) 2003-01-22 EP disclosed
EP-0716100-B1 Glazing for planes with light stability, chemical stability and heat distortion resistance ROEHM GMBH (DE) 1999-06-09 EP disclosed
EP-0902810-A1 THERMOPLASTIC MOULDED MATERIALS BASED ON POLYCARBONATES AND STYRENE/ACRYLONITRILE POLYMERS WHICH CONTAIN COPOLYMERS BASED ON ALKYL(METH)ACRYLATE TO IMPROVE THEIR PROPERTIES BASF AKTIENGESELLSCHAFT (DE) 1999-03-24 EP disclosed
WO-1997045484-A1 THERMOPLASTIC MOULDED MATERIALS BASED ON POLYCARBONATES AND STYRENE/ACRYLONITRILE POLYMERS WHICH CONTAIN COPOLYMERS BASED ON ALKYL(METH)ACRYLATE TO IMPROVE THEIR PROPERTIES BASF AKTIENGESELLSCHAFT (DE) 1997-12-04 WO disclosed
EP-0716100-A1 Glazing for planes with improved light stability, improved chemical stability and improved heat distortion resistance Röhm GmbH (DE) 1996-06-12 EP disclosed
EP-0667777-A1 XANTHINE DERIVATIVES FOR USE AS DIURETICS BOEHRINGER INGELHEIM INTERNATIONAL GmbH (DE) 1995-08-23 EP disclosed
EP-0457147-B1 Polymer compositions ROEHM GMBH (DE) 1995-06-14 EP disclosed
WO-1994011000-A1 XANTHINE DERIVATIVES FOR USE AS DIURETICS BOEHRINGER INGELHEIM KG (DE) 1994-05-26 WO disclosed
EP-0457147-A1 Polymer compositions RÖHM GMBH (DE) 1991-11-21 EP disclosed