Fumaric Acid

Fumaric Acid

SCHEMBL7471789

CN(CCc1ccccc1)C1CCN(C(=O)c2ccc([N+](=O)[O-])cc2)CC1.O=C(O)/C=C/C(=O)O

nearest known ligand 0.59

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
KMT2A known ✓ Q03164 4/20 0.57
HTR2A known ✓ P28223 1/20 0.47
CHRM2 known ✓ P08172 1/20 0.46
CHRM3 known ✓ P20309 1/20 0.46
MEN1 known ✓ O00255 1/20 0.44
HTT P42858 2/20 0.59
PKM P14618 1/20 0.57
TAAR1 Q96RJ0 1/20 0.57
LMNA P02545 2/20 0.49
SMN1; SMN2 Q16637 4/20 0.47
ALDH1A1 P00352 2/20 0.47
MAPT P10636 1/20 0.46
MAPK1 P28482 1/20 0.46
TDP1 Q9NUW8 1/20 0.46
NPC1 O15118 1/20 0.45
RAB9A P51151 1/20 0.45
HSD11B1 P28845 1/20 0.44
MGLL Q99685 1/20 0.44
NPBWR1 P48145 1/20 0.44
MCHR1 Q99705 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 SCHEMBL7471795 1.00 HTT (0.59) HTTKMT2APKMTAAR1LMNA
Fumaric Acid SCHEMBL7477079 0.90 RXFP1 (0.49) HTTKMT2APKMTAAR1SMN1; SMN2
Fumaric Acid SCHEMBL7477072 0.90 RXFP1 (0.49) HTTKMT2APKMTAAR1SMN1; SMN2
Fumaric Acid SCHEMBL7300329 0.86 MAPT (0.53) HTTKMT2ASMN1; SMN2HTR2AALDH1A1
Fumaric Acid SCHEMBL9451626 0.86 MAPT (0.53) HTTKMT2ASMN1; SMN2HTR2AALDH1A1
Hydrochloric Acid SCHEMBL7470963 0.82 HTT (0.53) HTTKMT2APKMTAAR1LMNA
Hydrochloric Acid SCHEMBL7463749 0.81 HTT (0.54) HTTKMT2APKMTAAR1LMNA
SCHEMBL7465052 0.80 L3MBTL3 (0.52) KMT2ALMNAMEN1
SCHEMBL7472599 0.80 L3MBTL3 (0.52) KMT2ALMNAMGLLMEN1
Hydrochloric Acid SCHEMBL7476858 0.80 L3MBTL3 (0.52) KMT2ALMNAHSD11B1MEN1

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
EP-0650476-B1 PERIPHERAL VASODILATING AGENT CONTAINING N-ACYLATED 4-AMINO PIPERIDINE DERIVATIVES AS ACTIVE INGREDIENTS OTSUKA PHARMA CO LTD (JP) 2002-06-26 EP disclosed
US-6136826-A AMINOPIPERIDINE COMPOUNDS SUBSTITUTED WITH ALKANOYL OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2000-10-24 US disclosed
US-5656642-A Peripheral vasodilating agent containing piperidine derivative as active ingredient OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1997-08-12 US disclosed
WO-1994022826-A1 PERIPHERAL VASODILATING AGENT CONTAINING N-ACYLATED 4-AMINO PIPERIDINE DERIVATIVES AS ACTIVE INGREDIENTS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1994-10-13 WO disclosed