Succinic Acid

Succinic Acid

SCHEMBL508414

Clc1ccc2c(c1SCc1ccc(NC3CCCCC3)nc1)CCNCC2.O=C(O)CCC(=O)O

nearest known ligand 0.37

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 20)

geneUniProtsupporting neighboursconfidence
HTR2A known ✓ P28223 1/20 0.32
HTR2C known ✓ P28335 1/20 0.32
HCAR3 P49019 3/20 0.37
EPHX1 P07099 1/20 0.34
NMT2 O60551 2/20 0.34
NMT1 P30419 2/20 0.34
HTR2B P41595 1/20 0.32
S1PR1 P21453 3/20 0.31
CCNT1 O60563 1/20 0.31
RXFP1 Q9HBX9 1/20 0.31
GAA P10253 1/20 0.31
ITGB1 P05556 1/20 0.30
ITGA5 P08648 1/20 0.30
PRKAB2 O43741 1/20 0.30
PRKAG1 P54619 1/20 0.30
PRKAA2 P54646 1/20 0.30
PRKAA1 Q13131 1/20 0.30
PRKAG3 Q9UGI9 1/20 0.30
PRKAG2 Q9UGJ0 1/20 0.30
PRKAB1 Q9Y478 1/20 0.30

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
SCHEMBL10230400 0.94 HTR2A (0.36) HCAR3EPHX1NMT2NMT1HTR2A
Succinic Acid SCHEMBL508666 0.89 TPH1 (0.36) HCAR3HTR2BCCNT1
Succinic Acid SCHEMBL508455 0.84 HCAR3 (0.38) HCAR3HTR2AHTR2CHTR2BCCNT1
Succinic Acid SCHEMBL507928 0.83 HTR2C (0.32) HTR2AHTR2CHTR2B
Succinic Acid SCHEMBL507927 0.83 HTR2A (0.32) HTR2AHTR2CHTR2B
Succinic Acid SCHEMBL507841 0.83 RXFP1 (0.43) RXFP1GAA
Succinic Acid SCHEMBL507926 0.82 HTR2A (0.31) HTR2AHTR2CHTR2B
SCHEMBL10230402 0.81 CCNT1 (0.36) HTR2AHTR2CHTR2BCCNT1
Succinic Acid SCHEMBL508454 0.78 HCAR3 (0.37) HCAR3HTR2AHTR2CHTR2BCCNT1
Succinic Acid SCHEMBL507022 0.78 CNR2 (0.41)

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 1/4885HCAR3 350/4885
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 1/4885HCAR3 388/4885

“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.