Fumaric Acid

Fumaric Acid

SCHEMBL10370455

CN1CCC(Oc2cccnc2C#N)C1.O=C(O)/C=C/C(=O)O

nearest known ligand 0.49

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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
▸ HRH1 known ✓ P35367 2/20 0.49
▸ CHRM3 known ✓ P20309 2/20 0.43
▸ MEN1 known ✓ O00255 1/20 0.38
▸ KMT2A known ✓ Q03164 1/20 0.38
▸ HTR2C known ✓ P28335 1/20 0.38
▸ HTR2B known ✓ P41595 1/20 0.38
▸ DRD2 known ✓ P14416 1/20 0.37
▸ CHRM4 P08173 2/20 0.43
▸ CHRM5 P08912 2/20 0.43
▸ CHRM1 P11229 2/20 0.43
▸ SCD O00767 1/20 0.41
▸ SMN1; SMN2 Q16637 2/20 0.39
▸ KDM4E B2RXH2 1/20 0.39
▸ NPY1R P25929 1/20 0.39
▸ NPY2R P49146 1/20 0.39
▸ CHEK1 O14757 1/20 0.38
▸ SSTR4 P31391 1/20 0.37
▸ ALDH1A1 P00352 2/20 0.37
▸ GMNN O75496 1/20 0.37
▸ LMNA P02545 1/20 0.37

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 SCHEMBL10370456 1.00 HRH1 (0.49) HRH1CHRM4CHRM5CHRM1CHRM3
Fumaric Acid SCHEMBL10372505 0.78 HRH1 (0.44) HRH1CHRM4CHRM5CHRM1CHRM3
Fumaric Acid SCHEMBL10370924 0.78 HRH1 (0.44) HRH1CHRM4CHRM5CHRM1CHRM3
SCHEMBL26506522 0.74 SCD (0.41) SCDCHEK1
SCHEMBL20472482 0.71 PDE5A (0.46) SCDCHEK1
SCHEMBL30541545 0.71 NOS3 (0.48) CHRM4CHRM5CHRM1CHRM3HTR2C
SCHEMBL26518454 0.70 PDE5A (0.45) SCDCHEK1
SCHEMBL3295720 0.70 SSTR4 (0.50) SSTR4
SCHEMBL30292528 0.70 KDM4E (0.55) HRH1CHRM4CHRM5CHRM1CHRM3
SCHEMBL15699577 0.69 GPR119 (0.52) SCD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0107930-B1 FUSED AROMATIC OXAZEPINONES AND SULPHUR ANALOGUES THEREOF AND THEIR PREPARATION AND USE IN COUNTERACTING HISTAMINE A.H. ROBINS COMPANY, INCORPORATED (a Delaware corporation) (US) 1990-11-28 — — EP disclosed
US-4812565-A ANTIHISTAMINE INTERMEDIATES A. H. ROBINS COMPANY, INCORPORATED (US) 1989-03-14 — — US disclosed
US-4810795-A ANTIHISTAMINES A. H. ROBINS COMPANY, INCORPORATED (US) 1989-03-07 — — US disclosed
US-4727152-A Intermediates useful in the preparation of fused aromatic oxazepinones, thiazepinones, diazepinones and sulfur analogs thereof A. H. ROBINS COMPANY, INC. (US) 1988-02-23 — — US disclosed
US-4705853-A ANTIHISTAMINES A. H. ROBINS COMPANY, INC. (US) 1987-11-10 — — US disclosed
US-4642343-A ANTIHISTAMINES A. H. ROBINS COMPANY, INCORPORATED (US) 1987-02-10 — — US disclosed
US-4604388-A Fused aromatic oxazepinones, thiazepinones, diazepinones and sulfur analogs thereof in a method of counteracting histamine A. H. ROBINS COMPANY, INCORPORATED (US) 1986-08-05 — — US disclosed
US-4592866-A Fused aromatic oxazepinones, thiazepinones, diazepinones and sulfur analogs thereof A. H. ROBINS COMPANY, INC. (US) 1986-06-03 — — US disclosed
EP-0107930-A2 Fused aromatic oxazepinones and sulphur analogues thereof and their preparation and use in counteracting histamine A.H. ROBINS COMPANY, INCORPORATED (a Delaware corporation) (US) 1984-05-09 — — EP disclosed
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