Fumaric Acid

Fumaric Acid

SCHEMBL747077

CN1[C@@H]2CC[C@H]1C[C@@H](Nc1ccc(-c3cccc4[nH]ccc34)cc1)C2.O=C(O)/C=C/C(=O)O

nearest known ligand 0.41

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 20)

geneUniProtsupporting neighboursconfidence
KCNH2 known ✓ Q12809 2/20 0.41
CHRNA7 P36544 2/20 0.41
KDM4E B2RXH2 1/20 0.41
HTR3E A5X5Y0 1/20 0.41
HTR3B O95264 1/20 0.41
HTR3A P46098 1/20 0.41
HTR3D Q70Z44 1/20 0.41
HTR3C Q8WXA8 1/20 0.41
HPGDS O60760 5/20 0.39
ATR Q13535 1/20 0.39
MCHR1 Q99705 1/20 0.39
PIK3CD O00329 1/20 0.38
PIM1 P11309 1/20 0.38
PIK3CB P42338 1/20 0.38
GSK3B P49841 1/20 0.38
ABL1 P00519 1/20 0.38
PIP4K2A P48426 1/20 0.38
PIP4K2B P78356 1/20 0.38
PIP4K2C Q8TBX8 1/20 0.38
IRAK4 Q9NWZ3 1/20 0.38

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 SCHEMBL747078 1.00 CHRNA7 (0.41) CHRNA7KCNH2KDM4EHTR3EHTR3B
SCHEMBL746815 0.91 CHRNA7 (0.45) CHRNA7KCNH2HTR3EHTR3BHTR3A
SCHEMBL746814 0.91 CHRNA7 (0.45) CHRNA7KCNH2HTR3EHTR3BHTR3A
Fumaric Acid SCHEMBL990090 0.86 CHRNA7 (0.42) CHRNA7KCNH2KDM4EHTR3EHTR3B
Fumaric Acid SCHEMBL990089 0.86 CHRNA7 (0.42) CHRNA7KCNH2KDM4EHTR3EHTR3B
SCHEMBL748909 0.81 IRAK4 (0.43) CHRNA7KCNH2HTR3EHTR3BHTR3A
SCHEMBL748910 0.81 IRAK4 (0.43) CHRNA7KCNH2HTR3EHTR3BHTR3A
Fumaric Acid SCHEMBL746341 0.80 PTGS2 (0.45) CHRNA7KCNH2KDM4EGSK3BABL1
Fumaric Acid SCHEMBL746342 0.80 PTGS2 (0.45) CHRNA7KCNH2KDM4EGSK3BABL1
Trifluoroacetic Acid SCHEMBL747098 0.80 HPGDS (0.39) CHRNA7KCNH2HTR3EHTR3BHTR3A

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 708/4885CHRNA7 2776/4885KDM4E 1947/4885
US-20100305089-A1 Fused Bicycloheterocycle Substituted Azabicyclic Alkane Derivatives MALT1, BMP2, ALKBH2 KCNH2 708/4885CHRNA7 2776/4885KDM4E 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.