Fumaric Acid

Fumaric Acid

SCHEMBL9540863

COc1cc([N+](=O)[O-])c2c(c1)[C@]1(C)CCN(C)[C@@H]1N2C.O=C(O)/C=C/C(=O)O

nearest known ligand 0.53

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
MEN1 known ✓ O00255 1/20 0.44
KMT2A known ✓ Q03164 1/20 0.44
KDM4E B2RXH2 5/20 0.53
ALDH1A1 P00352 3/20 0.53
SMN1; SMN2 Q16637 3/20 0.53
LMNA P02545 2/20 0.53
BLM P54132 2/20 0.53
MAPT P10636 2/20 0.53
G6PD P11413 1/20 0.53
GMNN O75496 1/20 0.53
THRB P10828 1/20 0.53
PMP22 Q01453 1/20 0.53
NPSR1 Q6W5P4 1/20 0.53
ACHE P22303 16/20 0.46
BCHE P06276 10/20 0.46
CYP2D6 P10635 2/20 0.44
CYP1A2 P05177 1/20 0.44
HIF1A Q16665 1/20 0.44
PTGS1 P23219 1/20 0.44
OPRM1 P35372 1/20 0.44

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 SCHEMBL9540869 1.00 KDM4E (0.53) KDM4EALDH1A1SMN1; SMN2LMNABLM
SCHEMBL2456588 0.92 ACHE (0.48) KDM4EALDH1A1SMN1; SMN2LMNABLM
SCHEMBL2456592 0.92 ACHE (0.48) KDM4EALDH1A1SMN1; SMN2LMNABLM
Fumaric Acid SCHEMBL8827778 0.90 KDM4E (0.51) KDM4EALDH1A1SMN1; SMN2LMNABLM
Fumaric Acid SCHEMBL8827775 0.85 KDM4E (0.61) KDM4EALDH1A1SMN1; SMN2LMNABLM
Fumaric Acid SCHEMBL8827779 0.85 KDM4E (0.61) KDM4EALDH1A1SMN1; SMN2LMNABLM
Fumaric Acid SCHEMBL9538223 0.85 KDM4E (0.54) KDM4EALDH1A1SMN1; SMN2LMNABLM
Fumaric Acid SCHEMBL9538218 0.85 KDM4E (0.54) KDM4EALDH1A1SMN1; SMN2LMNABLM
SCHEMBL2453702 0.84 ACHE (0.49) KDM4EALDH1A1SMN1; SMN2LMNABLM
SCHEMBL2598910 0.84 ACHE (0.49) KDM4EALDH1A1SMN1; SMN2LMNABLM

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
US-5187165-A Eseroline derivatives; cholinergic agents; antidepressants HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) 1993-02-16 US disclosed