Fumaric Acid

Fumaric Acid

SCHEMBL746383

CN1C2CCC1CC(Nc1ccc(-c3ccc4occc4c3)cc1)C2.O=C(O)/C=C/C(=O)O

nearest known ligand 0.56

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRB1ADRB2ATP4AATP4BAXLCHRM2CHRM3DRD2FLT3HRH1HTR2AHTR2BHTR2CKCNH2KMT2AMAP2K1MAP2K2MEN1MLNRPLK4RENS1PR1SLC6A2SLC6A4atpAatpBatpCatpDatpEatpFatpFHatpGpol

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 10)

geneUniProtsupporting neighboursconfidence
KCNH2 known ✓ Q12809 2/20 0.38
FFAR1 O14842 1/20 0.39
KDM4E B2RXH2 1/20 0.39
CNR1 P21554 1/20 0.39
CHRNA7 P36544 4/20 0.38
LTA4H P09960 2/20 0.38
CA12 O43570 3/20 0.36
CA2 P00918 2/20 0.36
FASN P49327 1/20 0.36
DYRK1A Q13627 1/20 0.36

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
Fumaric Acid SCHEMBL746382 1.00 FFAR1 (0.39) FFAR1KDM4ECNR1CHRNA7KCNH2
SCHEMBL748131 0.91 CHRNA7 (0.44) CNR1CHRNA7KCNH2CA12CA2
SCHEMBL748130 0.91 CHRNA7 (0.44) CNR1CHRNA7KCNH2CA12CA2
Fumaric Acid SCHEMBL744788 0.88 CHRNA7 (0.42) KDM4ECHRNA7KCNH2LTA4HFASN
Fumaric Acid SCHEMBL744787 0.88 CHRNA7 (0.42) KDM4ECHRNA7KCNH2LTA4HFASN
Fumaric Acid SCHEMBL748370 0.81 CCNC (0.43) KDM4ECHRNA7KCNH2LTA4HFASN
Fumaric Acid SCHEMBL748371 0.81 CCNC (0.43) KDM4ECHRNA7KCNH2LTA4HFASN
Fumaric Acid SCHEMBL746341 0.80 PTGS2 (0.45) KDM4ECHRNA7KCNH2FASNDYRK1A
Fumaric Acid SCHEMBL746342 0.80 PTGS2 (0.45) KDM4ECHRNA7KCNH2FASNDYRK1A
Fumaric Acid SCHEMBL989059 0.79 ROCK2 (0.52) DYRK1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2431368-B1 CNS active fused bicycloheterocycle substituted azabicyclic alkane derivatives ABBVIE BAHAMAS LTD (BS) 2014-08-27 EP disclosed
EP-2431368-A1 CNS active fused bicycloheterocycle substituted azabicyclic alkane derivatives Abbott Laboratories (US) 2012-03-21 EP disclosed
EP-2018380-B1 Cns active fused bicycloheterocycle substituted azabicyclic alkane derivatives ABBOTT LAB (US) 2011-10-19 EP disclosed
US-7872017-B2 Fused bicycloheterocycle substituted azabicyclic alkane derivatives ABBOTT LABORATORIES (US) 2011-01-18 US disclosed
US-20100305089-A1 Fused Bicycloheterocycle Substituted Azabicyclic Alkane Derivatives ABBOTT LABORATORIES (US) 2010-12-02 US disclosed
US-20080045539-A1 FUSED BICYCLOHETEROCYCLE SUBSTITUTED AZABICYCLIC ALKANE DERIVATIVES ABBVIE INC. 2008-02-21 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 (2 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-20080045539-A1 FUSED BICYCLOHETEROCYCLE SUBSTITUTED AZABICYCLIC ALKANE DERIVATIVES MALT1, BMP2, ALKBH2 KCNH2 708/4885FFAR1 1329/4885KDM4E 1947/4885
US-20100305089-A1 Fused Bicycloheterocycle Substituted Azabicyclic Alkane Derivatives MALT1, BMP2, ALKBH2 KCNH2 708/4885FFAR1 1329/4885KDM4E 1947/4885

“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.