Fumaric Acid

Fumaric Acid

SCHEMBL930663

C1CC2CCC2C1.O=C(O)C=CC(=O)O

nearest known ligand 0.50

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ATP4AATP4BAXLBTKCACNA1CCACNA1DCACNA1FCACNA1SCCR5CHRM2CHRM3CPT1BCPT2DPP4DRD1DRD2EGFRERBB2ERBB4FLT3HRH1HRH3HTR1AHTR2AHTR2BHTR2CHTR4JAK1JAK2JAK3KCNH2KMT2AMAP2K1MAP2K2MEN1MLNRMPLMTORPPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PLK4PPARGRENS1PR1SLC6A2SLC6A3SLC6A4SMOTYK2atpAatpBatpCatpDatpEatpFatpFHatpGpol

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 0.35
KMT2A known ✓ Q03164 1/20 0.35
TSHR P16473 2/20 0.50
TP53 P04637 2/20 0.50
EGLN1 Q9GZT9 1/20 0.50
EGLN3 Q9H6Z9 1/20 0.50
SMN1; SMN2 Q16637 3/20 0.45
GAA P10253 2/20 0.45
HTT P42858 2/20 0.45
NPC1 O15118 1/20 0.45
POLB P06746 1/20 0.44
ATM Q13315 1/20 0.42
THRB P10828 1/20 0.38
CYP2C9 P11712 1/20 0.38
ALDH1A1 P00352 2/20 0.37
HCAR2 Q8TDS4 2/20 0.36
LMNA P02545 2/20 0.35
MITF O75030 1/20 0.35
CYP3A4 P08684 1/20 0.35
MAPT P10636 1/20 0.35

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 SCHEMBL930661 1.00 TSHR (0.50) TSHRTP53EGLN1EGLN3SMN1; SMN2
Maleic Acid SCHEMBL29090331 0.92 TSHR (0.53) TSHRTP53EGLN1EGLN3SMN1; SMN2
Biphenyl SCHEMBL28905684 0.89 HTT (0.56) TSHRTP53EGLN1EGLN3SMN1; SMN2
Fumaric Acid SCHEMBL29080582 0.89 HTT (0.56) TSHRTP53EGLN1EGLN3SMN1; SMN2
Maleic Acid SCHEMBL28396018 0.89 HTT (0.56) TSHRTP53EGLN1EGLN3SMN1; SMN2
Biphenyl SCHEMBL4308447 0.89 HTT (0.56) TSHRTP53EGLN1EGLN3SMN1; SMN2
Bicarbonate SCHEMBL7186408 0.78 ALDH1A1 (0.50) TSHRTP53SMN1; SMN2NPC1POLB
Maleic Acid SCHEMBL31326366 0.78 TSHR (0.50) TSHRTP53EGLN1EGLN3SMN1; SMN2
Acrylic Acid SCHEMBL29117799 0.78 LMNA (0.56) TSHRSMN1; SMN2GAAHTTNPC1
Bicarbonate SCHEMBL5612384 0.76 ALDH1A1 (0.57) TSHRSMN1; SMN2NPC1POLBALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7872010-B2 Substituted diazabicycloalkane derivatives having affinity for nicotinic acetylcholine receptors ABBOTT LABORATORIES (US) 2011-01-18 US disclosed
US-20080275048-A1 Substituted Diazabicycloalkane Derivates ABBOTT LABORATORIES (US) 2008-11-06 US disclosed
US-7399765-B2 Substituted diazabicycloalkane derivatives ABBOTT LABORATORIES (US) 2008-07-15 US disclosed
US-20050101602-A1 For example, 3-(6-phenyl-pyridazin-3-yl)-3,8-diaza-bicyclo[3.2.1]octane; for treatment or prevention of conditions and disorders related to nAChR activity, and more particularly alpha 7 nAChR activity, such as attention deficit disorder, attention deficit hyperactivity disorder, Alzheimer's disease ABBVIE INC. 2005-05-12 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-20080275048-A1 Substituted Diazabicycloalkane Derivates CHRNA7, CHRNA1, CHRNA2 MEN1 3019/4885KMT2A 1656/4885TSHR 741/4885
US-20050101602-A1 For example, 3-(6-phenyl-pyridazin-3-yl)-3,8-diaza-bicyclo[3.2.1]octane; for treatment or prevention of conditions and disorders related to nAChR activity, and more particularly alpha 7 nAChR activity, such as attention deficit disorder, attention deficit hyperactivity disorder, Alzheimer's disease CHRNA7, CHRNA2, CHRNA6 MEN1 4343/4885KMT2A 1571/4885TSHR 1509/4885

“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.