Fumaric Acid

Fumaric Acid

SCHEMBL1177667

CN1C2CCC1CC(Oc1ccc(Cl)cn1)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 20)

geneUniProtsupporting neighboursconfidence
KCNH2 known ✓ Q12809 1/20 0.46
SLC6A2 known ✓ P23975 1/20 0.43
MEN1 known ✓ O00255 1/20 0.42
KMT2A known ✓ Q03164 1/20 0.42
DRD2 known ✓ P14416 1/20 0.42
CYP2D6 P10635 4/20 0.47
CYP2C19 P33261 2/20 0.47
LMNA P02545 1/20 0.47
OPRK1 P41145 1/20 0.46
MMP1 P03956 1/20 0.44
SLC6A3 Q01959 2/20 0.43
CYP1A2 P05177 3/20 0.43
TSHR P16473 3/20 0.43
HTR3E A5X5Y0 2/20 0.43
HTR3B O95264 2/20 0.43
HTR3A P46098 2/20 0.43
HTR3D Q70Z44 2/20 0.43
HTR3C Q8WXA8 2/20 0.43
GMNN O75496 1/20 0.43
ALOX15 P16050 1/20 0.43

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
SCHEMBL1177891 0.89 SLC6A3 (0.51) CYP2D6CYP2C19LMNAOPRK1KCNH2
SCHEMBL1177892 0.89 SLC6A3 (0.51) CYP2D6CYP2C19LMNAOPRK1KCNH2
Fumaric Acid SCHEMBL1177902 0.86 CYP2D6 (0.46) CYP2D6LMNAOPRK1KCNH2SLC6A3
Fumaric Acid SCHEMBL2236126 0.84 KCNH2 (0.54) OPRK1KCNH2MMP1
Fumaric Acid SCHEMBL2236115 0.84 KCNH2 (0.54) OPRK1KCNH2MMP1
Fumaric Acid SCHEMBL1178254 0.83 LIPE (0.48)
Fumaric Acid SCHEMBL1177616 0.82 SLC6A2 (0.44) CYP2D6CYP2C19LMNAOPRK1SLC6A3
Fumaric Acid SCHEMBL2236898 0.82 KCNH2 (0.57) OPRK1KCNH2
Fumaric Acid SCHEMBL2236891 0.82 KCNH2 (0.57) OPRK1KCNH2
Fumaric Acid SCHEMBL971277 0.81 ACACB (0.47) CYP2D6LMNAOPRK1KCNH2SLC6A3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110112139-A1 NOVEL 8-AZA-BICYCLO[3.2.1]OCTANE DERIVATIVES AND THEIR USE AS MONOAMINE NEUROTRANSMITTER RE-UPTAKE INHIBITORS PETERS DAN 2011-05-12 US disclosed
US-7888358-B2 Serotonine, dopamine and norendrenaline receptors; antidepressants, anxiolytic agents, eating disorders; obesity; bipolar; drug abuse; neurodegenerative diseases NEUROSEARCH A/S (DK) 2011-02-15 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-20110112139-A1 NOVEL 8-AZA-BICYCLO[3.2.1]OCTANE DERIVATIVES AND THEIR USE AS MONOAMINE NEUROTRANSMITTER RE-UPTAKE INHIBITORS SLC18A2, SLC18A3, SLC6A2 KCNH2 1266/4885SLC6A2 3/4885MEN1 2969/4885

“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.