Succinic Acid

Succinic Acid

SCHEMBL2992332

O=C(O)CC(C(=O)O)C1CC=CC1.O=C(O)CCC(=O)O

nearest known ligand 0.39

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
CYP1A2 P05177 2/20 0.39
TSHR P16473 1/20 0.39
FOLH1 Q04609 1/20 0.36
LMNA P02545 1/20 0.35
ALKBH5 Q6P6C2 1/20 0.35
SUCNR1 Q9BXA5 1/20 0.35
EGLN1 Q9GZT9 1/20 0.35
GRM8 O00222 1/20 0.33
GRM6 O15303 1/20 0.33
GRIN2D O15399 1/20 0.33
GRIN3B O60391 1/20 0.33
GSR P00390 1/20 0.33
GRIK1 P39086 1/20 0.33
GRM5 P41594 1/20 0.33
GRIA1 P42261 1/20 0.33
GRIA2 P42262 1/20 0.33
GRIA3 P42263 1/20 0.33
SLC1A3 P43003 1/20 0.33
SLC1A2 P43004 1/20 0.33
SLC1A1 P43005 1/20 0.33

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
SCHEMBL28601574 0.81 CYP1A2 (0.37) CYP1A2TSHRTDP1SMN1; SMN2ALDH1A1
SCHEMBL17376821 0.74 CPN1 (0.45) CYP1A2TSHRTDP1SMN1; SMN2ALDH1A1
SCHEMBL16249740 0.74 CPN1 (0.45) CYP1A2TSHRTDP1SMN1; SMN2ALDH1A1
SCHEMBL27598543 0.71 ALDH1A1 (0.47) CYP1A2TSHRTDP1SMN1; SMN2ALDH1A1
SCHEMBL13115586 0.71 ALDH1A1 (0.52) CYP1A2TSHRTDP1SMN1; SMN2ALDH1A1
SCHEMBL258779 0.69 ALDH1A1 (0.55) CYP1A2TSHRGRIK1TDP1SMN1; SMN2
SCHEMBL8133196 0.69 ALDH1A1 (0.55) CYP1A2TSHRGRIK1TDP1SMN1; SMN2
SCHEMBL6756443 0.69 ALDH1A1 (0.55) CYP1A2TSHRGRIK1TDP1SMN1; SMN2
SCHEMBL28167338 0.69 CYP1A2 (0.36) CYP1A2TSHRLMNATDP1ALDH1A1
SCHEMBL28968533 0.68 ALDH1A1 (0.53) CYP1A2TSHRGRIK1TDP1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8658796-B2 Complexes of ruthenium, method of production thereof and use thereof as (pre)catalysts of the metathesis reaction UMICORE AG & CO. KG (DE) 2014-02-25 US disclosed
US-20130079515-A1 Complexes of Ruthenium, Method of Production Thereof And Use Thereof As (Pre)Catalysts of the Metathesis Reaction UMICORE AG & CO. KG (DE) 2013-03-28 US disclosed
US-8318965-B2 Complex of ruthenium, method of production thereof and use thereof as (pre)catalysts of the metathesis reaction UMICORE AG & CO. KG (DE) 2012-11-27 US disclosed
US-20100174068-A1 Complex of Ruthenium and Osmium, Method of Production Thereof and Use Thereof As (Pre)Catalysts of the Metathesis Reaction UMICORE AG & CO KG (DE) 2010-07-08 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 (1 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-20130079515-A1 Complexes of Ruthenium, Method of Production Thereof And Use Thereof As (Pre)Catalysts of the Metathesis Reaction CBR3, CBR1, C1R CYP1A2 631/4885TSHR 233/4885FOLH1 4465/4885

“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.