Succinic Acid

Succinic Acid

SCHEMBL3330322

C1COCCN1.O=C(O)CCC(=O)O

nearest known ligand 0.52

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
KDM4E B2RXH2 3/20 0.52
MEN1 O00255 1/20 0.52
KMT2A Q03164 1/20 0.52
GAA P10253 1/20 0.52
CYP2C9 P11712 1/20 0.52
LMNA P02545 4/20 0.45
EGLN1 Q9GZT9 3/20 0.45
ALKBH5 Q6P6C2 1/20 0.45
SUCNR1 Q9BXA5 1/20 0.45
GLA P06280 1/20 0.43
HSD17B10 Q99714 1/20 0.37
SLC15A2 Q16348 1/20 0.36
MAPK1 P28482 1/20 0.36
SLC13A3 Q8WWT9 1/20 0.36
OR51E2 Q9H255 1/20 0.36
SLC22A6 Q4U2R8 1/20 0.35
KDM5C P41229 2/20 0.33
PHF8 Q9UPP1 2/20 0.33
KDM2A Q9Y2K7 2/20 0.33
TSHR P16473 2/20 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
Glutarate SCHEMBL27964714 0.91 SLC22A6 (0.50) KDM4EMEN1KMT2AGAACYP2C9
Sebacic Acid SCHEMBL27736944 0.89 TSHR (0.52) KDM4EMEN1KMT2AGAACYP2C9
Morpholine SCHEMBL11191668 0.87 FFAR3 (0.54) KDM4EMEN1KMT2AGAACYP2C9
Morpholine SCHEMBL9162514 0.85 MEN1 (0.52) KDM4EMEN1KMT2AGAACYP2C9
Morpholine SCHEMBL4018377 0.84 MEN1 (0.65) KDM4EMEN1KMT2AGAACYP2C9
Morpholine SCHEMBL14957611 0.84 MEN1 (0.65) KDM4EMEN1KMT2AGAACYP2C9
Morpholine SCHEMBL11524539 0.84 MEN1 (0.65) KDM4EMEN1KMT2AGAACYP2C9
Succinic Acid SCHEMBL8731618 0.84 LMNA (0.64) KDM4EKMT2ALMNAEGLN1ALKBH5
Valeric Acid SCHEMBL8526265 0.83 AKR1B1 (0.50) KDM4EMEN1KMT2AGAACYP2C9
Malonic Acid SCHEMBL28388411 0.83 MEN1 (0.50) KDM4EMEN1KMT2AGAACYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100137316-A1 Morpholine Compounds, Pharmaceutically Acceptable Salts Thereof, Pharmaceutical Compositions, and Methods Of Use Thereof FISH PAUL VINCENT 2010-06-03 US disclosed
CN-1950089-A Morpholine compounds PFIZER LTD (US) 2007-04-18 CN disclosed
EP-1744754-A1 MORPHOLINE COMPOUNDS Pfizer Limited (GB) 2007-01-24 EP disclosed
WO-2005105100-A1 MORPHOLINE COMPOUNDS PFIZER LIMITED (GB) 2005-11-10 WO disclosed
US-3963730-A ACID CATALYST SANKYO COMPANY LIMITED (JA) 1976-06-15 US disclosed
US-3959298-A ACETONINE WITH WATER IN ACID CATALYST SANKYO COMPANY LIMITED (JA) 1976-05-25 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-20100137316-A1 Morpholine Compounds, Pharmaceutically Acceptable Salts Thereof, Pharmaceutical Compositions, and Methods Of Use Thereof OPRL1, UGT1A1, HTR3B KDM4E 1680/4885MEN1 776/4885KMT2A 2356/4885

“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.