Succinic Acid

Succinic Acid

SCHEMBL507289

Fc1cc(Oc2ccccc2)ccc1CSc1c(Cl)ccc2c1CCNCC2.O=C(O)CCC(=O)O

nearest known ligand 0.35

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRB1CDK4CDK6CHRM2CHRM3DPP4DRD2DRD3DRD4EGFRHRH1HTR1BHTR1DHTR1FHTR2AHTR2CHTR4SLC6A2SLC6A4

The experimentally established mechanism targets of Succinic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
HTR2A known ✓ P28223 2/20 0.34
HTR2C known ✓ P28335 2/20 0.34
PPARG P37231 4/20 0.35
PPARA Q07869 4/20 0.35
PPARD Q03181 1/20 0.35
FFAR1 O14842 7/20 0.35
FFAR4 Q5NUL3 4/20 0.35
HTR2B P41595 2/20 0.34
RXRA P19793 1/20 0.33
RXRB P28702 1/20 0.33
RXRG P48443 1/20 0.33
GPR17 Q13304 1/20 0.31
ALDH1A1 P00352 1/20 0.31
MAPK1 P28482 1/20 0.31
MEN1 O00255 1/20 0.31
KMT2A Q03164 1/20 0.31
ATM Q13315 1/20 0.31

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
SCHEMBL10229169 0.94 HTR2B (0.38) HTR2AHTR2CHTR2B
Succinic Acid SCHEMBL507737 0.82 PPARG (0.35) PPARGPPARAPPARDFFAR1FFAR4
SCHEMBL10476259 0.78 CYP1A2 (0.42) HTR2AHTR2CHTR2BALDH1A1
SCHEMBL10228818 0.78 HTR2C (0.47) HTR2AHTR2CHTR2BALDH1A1MAPK1
SCHEMBL506629 0.77 MAPT (0.40)
Hydrochloric Acid SCHEMBL10476186 0.77 CYP1A2 (0.41) HTR2AHTR2CHTR2BALDH1A1
Succinic Acid SCHEMBL507163 0.77 FFAR4 (0.42) FFAR1FFAR4HTR2CHTR2BRXRA
Hydrochloric Acid SCHEMBL507832 0.77 HTR2C (0.46) HTR2AHTR2CHTR2BALDH1A1MAPK1
Succinic Acid SCHEMBL507172 0.76 PPARD (0.45) PPARGPPARAPPARDFFAR1FFAR4
Succinic Acid SCHEMBL507555 0.75 RXRG (0.34) HTR2AHTR2CHTR2BRXRARXRB

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
US-8580780-B2 6 substituted 2, 3,4,5 tetrahydro-1H-benzo[d]azepines as 5-HT2C receptor agonist ELI LILLY AND COMPANY (US) 2013-11-12 US disclosed
EP-2479168-A1 6-Substituted 2,3,4,5-Tetrahydro-1H-Benzo [d]Azepines as 5-HT2C Receptor Agonists ELI LILLY AND COMPANY (US) 2012-07-25 EP disclosed
US-20120028961-A1 6 Substituted 2, 3,4,5 Tetrahydro-1H-Benzo[d]Azepines as 5-HT2c Receptor Agonist ELI LILLY AND COMPANY (US) 2012-02-02 US disclosed
US-8022062-B2 6-substituted 2,3,4,5-tetrahydro-1H-benzo[d]azepines as 5-HT2C receptor agonists ELI LILLY AND COMPANY (US) 2011-09-20 US disclosed
US-20090099155-A1 6-SUBSTITUTED 2,3,4,5-TETRAHYDRO-1H-BENZO[D]AZEPINES AS 5-HT2C RECEPTOR AGONISTS ARRAY BIOPHARMA, INC. 2009-04-16 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 (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-20090099155-A1 6-SUBSTITUTED 2,3,4,5-TETRAHYDRO-1H-BENZO[D]AZEPINES AS 5-HT2C RECEPTOR AGONISTS HTR2C, HTR5A, HTR4 HTR2A 4/4885HTR2C 1/4885PPARG 1057/4885
US-20120028961-A1 6 Substituted 2, 3,4,5 Tetrahydro-1H-Benzo[d]Azepines as 5-HT2c Receptor Agonist HTR2C, HTR4, HTR1A HTR2A 4/4885HTR2C 1/4885PPARG 976/4885

“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.