Fumaric Acid

Fumaric Acid

SCHEMBL6501560

CNCC[C@@H](Oc1cc(C(F)(F)F)ccc1Cl)c1ccccc1.O=C(O)/C=C/C(=O)O

nearest known ligand 0.76

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
SLC6A4 known ✓ P31645 12/20 0.61
SLC6A2 known ✓ P23975 7/20 0.61
KMT2A known ✓ Q03164 6/20 0.56
MEN1 known ✓ O00255 5/20 0.56
HTR2C known ✓ P28335 4/20 0.56
HTR2A known ✓ P28223 3/20 0.56
HRH1 known ✓ P35367 3/20 0.56
HTR2B known ✓ P41595 3/20 0.56
KCNH2 known ✓ Q12809 3/20 0.56
CHRM2 known ✓ P08172 1/20 0.56
DRD2 known ✓ P14416 1/20 0.56
CHRM3 known ✓ P20309 1/20 0.56
NOS2 P35228 4/20 0.76
CYP2D6 P10635 8/20 0.61
CYP3A4 P08684 6/20 0.56
LMNA P02545 5/20 0.56
CYP1A2 P05177 5/20 0.56
SLC6A3 Q01959 4/20 0.56
TSHR P16473 4/20 0.56
CYP2C19 P33261 3/20 0.56

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 SCHEMBL6501568 1.00 NOS2 (0.76) NOS2SLC6A4CYP2D6SLC6A2KMT2A
SCHEMBL6502159 0.92 NOS2 (0.72) NOS2SLC6A4CYP2D6SLC6A2KMT2A
SCHEMBL6502153 0.92 NOS2 (0.72) NOS2SLC6A4CYP2D6SLC6A2KMT2A
Fumaric Acid SCHEMBL6491990 0.86 NOS2 (1.00) NOS2SLC6A4CYP2D6SLC6A2KMT2A
Fumaric Acid SCHEMBL6491175 0.86 NOS2 (1.00) NOS2SLC6A4CYP2D6SLC6A2KMT2A
Fumaric Acid SCHEMBL6501362 0.85 NOS2 (0.80) NOS2SLC6A4CYP2D6SLC6A2KMT2A
Fumaric Acid SCHEMBL6501358 0.85 NOS2 (0.80) NOS2SLC6A4CYP2D6SLC6A2KMT2A
Fluoxetine SCHEMBL27334900 0.83 SLC6A4 (0.82) NOS2SLC6A4CYP2D6SLC6A2KMT2A
Fluoxetine SCHEMBL6005182 0.83 SLC6A4 (0.82) NOS2SLC6A4CYP2D6SLC6A2KMT2A
Fluoxetine SCHEMBL6005177 0.83 SLC6A4 (0.82) NOS2SLC6A4CYP2D6SLC6A2KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6887871-B2 Use of phenylheteroakylamine derivatives ASTRAZENECA AB (SE) 2005-05-03 US disclosed
EP-1263711-B1 NOVEL USE OF PHENYLHETEROALKYLAMINE DERIVATIVES ASTRAZENECA AB (SE) 2004-12-15 EP disclosed
US-20030158185-A1 Novel use of phenylheteroakylamine derivatives ASTRAZENECA AB (SE) 2003-08-21 US disclosed
EP-1263711-A1 NOVEL USE OF PHENYLHETEROALKYLAMINE DERIVATIVES AstraZeneca AB (SE) 2002-12-11 EP disclosed
WO-2001062704-A1 NOVEL USE OF PHENYLHETEROALKYLAMINE DERIVATIVES ASTRAZENECA AB (SE) 2001-08-30 WO 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-20030158185-A1 Novel use of phenylheteroakylamine derivatives NOS1, XDH, NOS2 SLC6A4 2468/4885SLC6A2 1776/4885KMT2A 3267/4885

“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.