Fumaric Acid

Fumaric Acid

SCHEMBL7477072

CN(CCc1ccccc1)C1CCN(C(=O)c2cccc([N+](=O)[O-])c2)CC1.O=C(O)/C=C/C(=O)O

nearest known ligand 0.49

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 3/20 0.48
MEN1 known ✓ O00255 1/20 0.44
RXFP1 Q9HBX9 1/20 0.49
ALDH1A1 P00352 4/20 0.48
HTT P42858 3/20 0.48
MGLL Q99685 1/20 0.48
HSD11B1 P28845 1/20 0.48
KDM4E B2RXH2 1/20 0.47
CCR5 P51681 1/20 0.47
PKM P14618 1/20 0.46
TAAR1 Q96RJ0 1/20 0.46
SMN1; SMN2 Q16637 3/20 0.44
NPBWR1 P48145 1/20 0.44
MCHR1 Q99705 1/20 0.44
CA12 O43570 1/20 0.44
CA1 P00915 1/20 0.44
CA2 P00918 1/20 0.44
CA7 P43166 1/20 0.44
CA9 Q16790 1/20 0.44
CA14 Q9ULX7 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 SCHEMBL7477079 1.00 RXFP1 (0.49) RXFP1ALDH1A1HTTKMT2AMGLL
Fumaric Acid SCHEMBL7471789 0.90 HTT (0.59) ALDH1A1HTTKMT2AMGLLHSD11B1
Fumaric Acid SCHEMBL7471795 0.90 HTT (0.59) ALDH1A1HTTKMT2AMGLLHSD11B1
Hydrochloric Acid SCHEMBL7463749 0.81 HTT (0.54) ALDH1A1HTTKMT2APKMTAAR1
Fumaric Acid SCHEMBL9451626 0.80 MAPT (0.53) ALDH1A1HTTKMT2ASMN1; SMN2MEN1
Fumaric Acid SCHEMBL7300329 0.80 MAPT (0.53) ALDH1A1HTTKMT2ASMN1; SMN2MEN1
SCHEMBL7470703 0.80 LMNA (0.53) ALDH1A1HTTKMT2APKMTAAR1
Hydrochloric Acid SCHEMBL7470963 0.80 HTT (0.53) ALDH1A1HTTKMT2APKMTAAR1
Hydrochloric Acid SCHEMBL7462403 0.80 SMN1; SMN2 (0.68) ALDH1A1HTTKMT2AKDM4EPKM
SCHEMBL7463618 0.80 MGLL (0.48) ALDH1A1KMT2AMGLLSMN1; SMN2MEN1

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
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
EP-0650476-A1 PERIPHERAL VASODILATING AGENT CONTAINING N-ACYLATED 4-AMINO PIPERIDINE DERIVATIVES AS ACTIVE INGREDIENTS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1995-05-03 EP 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