Fumaric Acid

Fumaric Acid

SCHEMBL654314

N#Cc1cncc(N2CC[C@H]3CNC[C@H]32)c1.O=C(O)/C=C/C(=O)O

nearest known ligand 0.64

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 8)

geneUniProtsupporting neighboursconfidence
HTR2A known ✓ P28223 2/20 0.43
HTR2C known ✓ P28335 2/20 0.43
HTR2B known ✓ P41595 2/20 0.43
CHRNB2 P17787 15/20 0.64
CHRNA4 P43681 15/20 0.64
CHRNB4 P30926 12/20 0.64
CHRNA3 P32297 12/20 0.64
HRH3 Q9Y5N1 1/20 0.52

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 SCHEMBL654315 1.00 CHRNB2 (0.64) CHRNB2CHRNA4CHRNB4CHRNA3HRH3
Fumaric Acid SCHEMBL653894 1.00 CHRNB2 (0.64) CHRNB2CHRNA4CHRNB4CHRNA3HRH3
Fumaric Acid SCHEMBL653893 1.00 CHRNB2 (0.64) CHRNB2CHRNA4CHRNB4CHRNA3HRH3
Fumaric Acid SCHEMBL653539 0.90 CHRNB2 (0.80) CHRNB2CHRNA4CHRNB4CHRNA3
Fumaric Acid SCHEMBL653540 0.90 CHRNB2 (0.80) CHRNB2CHRNA4CHRNB4CHRNA3
SCHEMBL649630 0.90 CHRNB2 (0.78) CHRNB2CHRNA4CHRNB4CHRNA3HRH3
SCHEMBL651544 0.90 CHRNB2 (0.78) CHRNB2CHRNA4CHRNB4CHRNA3HRH3
Fumaric Acid SCHEMBL649959 0.86 CHRNB2 (0.81) CHRNB2CHRNA4CHRNB4CHRNA3
Fumaric Acid SCHEMBL652597 0.86 CHRNB2 (0.81) CHRNB2CHRNA4CHRNB4CHRNA3
Fumaric Acid SCHEMBL652598 0.86 CHRNB2 (0.81) CHRNB2CHRNA4CHRNB4CHRNA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20120208820-A1 DIAZABICYCLIC CENTRAL NERVOUS SYSTEM ACTIVE AGENTS SCHRIMPF MICHAEL R (US) 2012-08-16 US disclosed
US-8119635-B2 Diazabicyclic central nervous system active agents ABBOTT LABORATORIES (US) 2012-02-21 US disclosed
EP-2298775-A1 Diazabicyclic central nervous system active agents Abbott Laboratories (US) 2011-03-23 EP disclosed
EP-2295437-A1 Diazabicyclic central nervous system active agents Abbott Laboratories (US) 2011-03-16 EP disclosed
US-20100016277-A1 DIAZABICYCLIC CENTRAL NERVOUS SYSTEM ACTIVE AGENTS ABBOTT LABORATORIES (US) 2010-01-21 US disclosed
US-7598236-B2 Diazabicyclic central nervous system active agents ABBOTT LABORATORIES (US) 2009-10-06 US disclosed
US-20080097094-A1 DIAZABICYCLIC CENTRAL NERVOUS SYSTEM ACTIVE AGENTS ABBOTT LABORATORIES (US) 2008-04-24 US disclosed
US-7319106-B2 Diazabicyclic central nervous system active agents ABBOTT LABORATORIES (US) 2008-01-15 US disclosed
US-6809105-B2 (CIS)-6-(3-PYRIDINYL)-3,6-DIAZABICYCLO(3.2.0) HEPTANE FOR EXAMPLE; ALZHEIMER'S DISEASE, PARKINSON'S DISEASE, ATTENTION DEFICIT HYPERACTIVITY DISORDER, DEPRESSION, NICOTINIC WITHDRAWAL SYNDROME, TOURETTE'S SYNDROME, AND SCHIZOPHRENIA ABBOTT LABORATORIES 2004-10-26 US disclosed
US-20040186107-A1 Diazabicyclic central nervous system active agents ABBVIE INC. 2004-09-23 US disclosed
US-20020019388-A1 Diazabicyclic central nervous system active agents ABBVIE INC. 2002-02-14 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 (5 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-20080097094-A1 DIAZABICYCLIC CENTRAL NERVOUS SYSTEM ACTIVE AGENTS GAP43, GABRE, CHRNA6 HTR2A 1259/4885HTR2C 940/4885HTR2B 756/4885
US-20120208820-A1 DIAZABICYCLIC CENTRAL NERVOUS SYSTEM ACTIVE AGENTS GAP43, GABRE, CHRNA6 HTR2A 1259/4885HTR2C 940/4885HTR2B 756/4885
US-20020019388-A1 Diazabicyclic central nervous system active agents GAP43, GABRE, CHRNA6 HTR2A 1346/4885HTR2C 969/4885HTR2B 865/4885
US-20100016277-A1 DIAZABICYCLIC CENTRAL NERVOUS SYSTEM ACTIVE AGENTS GAP43, GABRE, CHRNA6 HTR2A 1259/4885HTR2C 940/4885HTR2B 756/4885
US-20040186107-A1 Diazabicyclic central nervous system active agents GAP43, GABRE, CHRNA6 HTR2A 1346/4885HTR2C 969/4885HTR2B 865/4885

“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.