Fumaric Acid

Fumaric Acid

SCHEMBL2054350

O=C(O)C=CC(=O)O.O=C1C=CC(=O)C=C1

nearest known ligand 0.56

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
KMT2A known ✓ Q03164 1/20 0.41
DPP4 known ✓ P27487 1/20 0.37
TSHR P16473 2/20 0.56
TP53 P04637 1/20 0.56
EGLN1 Q9GZT9 1/20 0.56
EGLN3 Q9H6Z9 1/20 0.56
ALDH1A1 P00352 4/20 0.50
BCHE P06276 1/20 0.50
POLB P06746 1/20 0.50
MAOA P21397 1/20 0.50
ACHE P22303 1/20 0.50
MAOB P27338 1/20 0.50
APEX1 P27695 1/20 0.50
MAPK1 P28482 1/20 0.50
CASP1 P29466 1/20 0.50
RECQL P46063 1/20 0.50
BLM P54132 1/20 0.50
MDM2 Q00987 1/20 0.50
DHODH Q02127 1/20 0.50
HSD17B10 Q99714 1/20 0.50

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 SCHEMBL2054349 1.00 TSHR (0.56) TSHRTP53EGLN1EGLN3ALDH1A1
Benzoquinone SCHEMBL31055608 0.79 ALDH1A1 (0.67) TSHRTP53ALDH1A1BCHEPOLB
Benzoquinone SCHEMBL27519977 0.79 ALDH1A1 (0.67) TSHRTP53ALDH1A1BCHEPOLB
Benzoquinone SCHEMBL28211057 0.79 TDP1 (0.80) TP53ALDH1A1BCHEPOLBMAOA
Benzoquinone SCHEMBL8966070 0.79 TDP1 (0.80) TP53ALDH1A1BCHEPOLBMAOA
Benzoquinone SCHEMBL8619522 0.79 LMNA (0.59) TSHRTP53EGLN1EGLN3ALDH1A1
Maleic Acid SCHEMBL27583410 0.75 TSHR (0.82) TSHRTP53EGLN1EGLN3ALDH1A1
Maleic Acid SCHEMBL2046430 0.75 TSHR (1.00) TSHRTP53EGLN1EGLN3ALDH1A1
Fumaric Acid SCHEMBL3998225 0.75
Maleic Acid SCHEMBL20487516 0.75 TSHR (1.00) TSHRTP53EGLN1EGLN3ALDH1A1

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-9278909-B2 Amide-extended crosslinking compounds and methods for use thereof DESIGNER MOLECULES, INC. (US) 2016-03-08 US disclosed
US-8637611-B2 Amide-extended crosslinking compounds and methods for use thereof DESIGNER MOLECULES, INC. (US) 2014-01-28 US disclosed
US-20130338313-A1 AMIDE-EXTENDED CROSSLINKING COMPOUNDS AND METHODS FOR USE THEREOF DESIGNER MOLECULES, INC. (US) 2013-12-19 US disclosed
US-20110152466-A1 AMIDE-EXTENDED CROSSLINKING COMPOUNDS AND METHODS FOR USE THEREOF DESIGNER MOLECULES, INC. (US) 2011-06-23 US disclosed
WO-2010019832-A2 AMIDE-EXTENDED CROSSLINKING COMPOUNDS AND METHODS FOR USE THEREOF DESIGNER MOLECULES, INC. (US) 2010-02-18 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-20110152466-A1 AMIDE-EXTENDED CROSSLINKING COMPOUNDS AND METHODS FOR USE THEREOF ACMSD, AAAS, NAAA KMT2A 78/4885DPP4 3770/4885TSHR 4318/4885

“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.