Fumaric Acid

Fumaric Acid

SCHEMBL5935166

CCCCOCCCC.O=C(O)C=CC(=O)O

nearest known ligand 0.67

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ATP4AATP4BAXLBTKCACNA1CCACNA1DCACNA1FCACNA1SCCR5CHRM2CHRM3CPT1BCPT2DPP4DRD1DRD2EGFRERBB2ERBB4FLT3HRH1HRH3HTR1AHTR2AHTR2BHTR2CHTR4JAK1JAK2JAK3KCNH2KMT2AMAP2K1MAP2K2MEN1MLNRMPLMTORPPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PLK4PPARGRENS1PR1SLC6A2SLC6A3SLC6A4SMOTYK2atpAatpBatpCatpDatpEatpFatpFHatpGpol

The experimentally established mechanism targets of Fumaric Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
HCAR2 Q8TDS4 5/20 0.67
TSHR P16473 5/20 0.52
ATM Q13315 1/20 0.52
CYP3A4 P08684 1/20 0.45
ALDH1A1 P00352 1/20 0.44
CES2 O00748 1/20 0.43
HPGD P15428 1/20 0.43
TP53 P04637 1/20 0.43
EGLN1 Q9GZT9 1/20 0.43
EGLN3 Q9H6Z9 1/20 0.43
RARB P10826 1/20 0.42

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 SCHEMBL12981050 1.00 HCAR2 (0.67) HCAR2TSHRATMCYP3A4ALDH1A1
Butoxyethanol SCHEMBL8736361 0.92 TSHR (0.68) HCAR2TSHRATMCYP3A4ALDH1A1
Fumaric Acid SCHEMBL12980929 0.91 HCAR2 (0.69) HCAR2CES2
Maleic Acid SCHEMBL12980928 0.91 HCAR2 (0.69) HCAR2CES2
Maleic Acid SCHEMBL30040841 0.90 HCAR2 (0.56) HCAR2TSHRATMCYP3A4ALDH1A1
Maleic Acid SCHEMBL29143549 0.90 HCAR2 (0.56) HCAR2TSHRATMCYP3A4ALDH1A1
Maleic Acid SCHEMBL29143547 0.90 HCAR2 (0.56) HCAR2TSHRATMCYP3A4ALDH1A1
Crotonic Acid SCHEMBL28102986 0.89 HCAR2 (0.55) HCAR2TSHRATMCYP3A4ALDH1A1
SCHEMBL2890706 0.87 HCAR2 (0.79) HCAR2TSHRATMCYP3A4ALDH1A1
SCHEMBL2898517 0.87 HCAR2 (0.79) HCAR2TSHRATMCYP3A4ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111848394-A Synthesis method and application of maleic acid dihydric alcohol mono-tertiary butyl ether diester 深圳飞扬兴业科技有限公司 2020-10-30 CN disclosed
US-20120258249-A1 LOW/ZERO VOC GLYCOL ETHER-ESTERS AS COALESCENTS FOR AQUEOUS POLYMERIC DISPERSIONS ADAMSON LINDA A (US) 2012-10-11 US disclosed
US-20060173102-A1 Synthetic material dispersions AMI-AGROLINZ MELAMINE INTERNATIONAL GMBH (AT) 2006-08-03 US 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-20120258249-A1 LOW/ZERO VOC GLYCOL ETHER-ESTERS AS COALESCENTS FOR AQUEOUS POLYMERIC DISPERSIONS HDLBP, COG7, COG4 HCAR2 1290/4885TSHR 4758/4885ATM 4571/4885

“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.