Maleic Acid

Maleic Acid

SCHEMBL21750113

COc1ccc(CC(C)(C)N)cc1.O=C(O)/C=C\C(=O)O

nearest known ligand 0.55

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2BTKCACNA1CCACNA1DCACNA1FCACNA1SCCR5CPT1BCPT2DPP4DRD1DRD2EGFRERBB2ERBB4HRH1HRH3HTR1AHTR2AHTR2BHTR2CHTR4JAK1JAK2JAK3MPLMTORPPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PPARGSLC6A2SLC6A3SLC6A4SMOTYK2pol

The experimentally established mechanism targets of Maleic 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
SLC6A2 known ✓ P23975 2/20 0.47
HTR2A known ✓ P28223 1/20 0.44
SLC6A4 known ✓ P31645 1/20 0.44
HRH1 known ✓ P35367 1/20 0.44
HTR2B known ✓ P41595 1/20 0.44
SLC6A3 known ✓ Q01959 1/20 0.44
ALDH1A1 P00352 3/20 0.55
TAAR1 Q96RJ0 2/20 0.55
THRB P10828 1/20 0.51
ATM Q13315 1/20 0.51
LDHA P00338 1/20 0.47
MMP1 P03956 1/20 0.47
MMP13 P45452 1/20 0.47
SMN1; SMN2 Q16637 3/20 0.45
HTT P42858 2/20 0.45
CHRNA4 P43681 1/20 0.44
NPC1 O15118 1/20 0.43
POLB P06746 1/20 0.43
RAB9A P51151 1/20 0.43
CTBP2 P56545 1/20 0.43

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
Acetic Acid SCHEMBL28687879 0.90 SLC6A2 (0.50) ALDH1A1TAAR1LDHASLC6A2MMP1
SCHEMBL183751 0.86 SLC6A2 (0.57) ALDH1A1TAAR1SLC6A2SMN1; SMN2HTR2A
Fumaric Acid SCHEMBL8867443 0.86 ALDH1A1 (0.48) ALDH1A1TAAR1THRBATMMMP1
Maleic Acid SCHEMBL8867414 0.86 ALDH1A1 (0.48) ALDH1A1TAAR1THRBATMMMP1
Cadaverine Tartrate SCHEMBL20298290 0.84 LDHA (0.53) TAAR1LDHASLC6A2MMP1MMP13
Tartaric Acid SCHEMBL30628113 0.84 LDHA (0.53) TAAR1LDHASLC6A2MMP1MMP13
Iodide SCHEMBL28694310 0.84 SLC6A2 (0.55) ALDH1A1TAAR1SLC6A2SMN1; SMN2HTR2A
Hydrochloric Acid SCHEMBL3800374 0.84 SLC6A2 (0.55) ALDH1A1TAAR1SLC6A2HTR2ASLC6A4
Bromide SCHEMBL28700901 0.84 SLC6A2 (0.55) ALDH1A1TAAR1SLC6A2SMN1; SMN2HTR2A
Sulfuric Acid SCHEMBL28679089 0.83 PTPRB (0.49) TAAR1LDHASLC6A2MMP1MMP13

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
CN-110114346-B Improved process for preparing R-6-hydroxy-8- [ 1-hydroxy-2- [2- (4-methoxyphenyl) -1, 1-dimethylethylaminoethyl ] -2H-1, 4-benzoxazin-3 (4H) -one hydrochloride INKE股份公司 2023-10-31 CN disclosed
EP-3558954-B1 IMPROVED PROCESS FOR THE MANUFACTURE OF R-6-HYDROXY-8-[1-HYDROXY-2-[2-(4-METHOXYPHENYL)-1,1-DIMETHYLETHYLAMINOETHYL]-2H-1,4-BENZOXAZIN-3(4H)-ONE HYDROCHLORIDE INKE SA (ES) 2021-11-03 EP disclosed
US-10800748-B2 Process for the manufacture of R-6-hydroxy-8-[1-hydroxy-2-[2-(4-methoxyphenyl)-1,1-dimethylethylaminoethyl]-2H-1,4-benzoxazin-3(4H)-one hydrochloride INKE, S.A. (ES) 2020-10-13 US disclosed
US-20200062723-A1 IMPROVED PROCESS FOR THE MANUFACTURE OF R-6-HYDROXY-8-[1-HYDROXY-2-[2-(4-METHOXYPHENYL)-1,1-DIMETHYLETHYLAMINOETHYL]-2H-1,4-BENZOXAZIN-3(4H)-ONE HYDROCHLORIDE LABORATORIOS LESVI, S.L. (ES) 2020-02-27 US disclosed
CN-110114346-A Improved process for the preparation of R-6-hydroxy-8- [ 1-hydroxy-2- [2- (4-methoxyphenyl) -1, 1-dimethylethylaminoethyl ] -2H-1, 4-benzoxazin-3 (4H) -one hydrochloride INKE股份公司 2019-08-09 CN 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 (2 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-20200062723-A1 IMPROVED PROCESS FOR THE MANUFACTURE OF R-6-HYDROXY-8-[1-HYDROXY-2-[2-(4-METHOXYPHENYL)-1,1-DIMETHYLETHYLAMINOETHYL]-2H-1,4-BENZOXAZIN-3(4H)-ONE HYDROCHLORIDE HTR6, HTR4, HAAO SLC6A2 97/4885HTR2A 71/4885SLC6A4 19/4885
US-10800748-B2 Process for the manufacture of R-6-hydroxy-8-[1-hydroxy-2-[2-(4-methoxyphenyl)-1,1-dimethylethylaminoethyl]-2H-1,4-benzoxazin-3(4H)-one hydrochloride HTR6, HTR4, SLC6A6 SLC6A2 69/4885HTR2A 72/4885SLC6A4 6/4885

“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.