Citric Acid

Citric Acid

SCHEMBL4333388

Cc1cc(-c2cccnc2)cc2c1C(=O)N(C1CCCC1)C2.O=C(O)CC(O)(CC(=O)O)C(=O)O

nearest known ligand 0.43

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACVR1ADORA1ADORA2AADORA2BADORA3ESR1ESR2FLT3GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSC1HRH1HTR7IDH1IDH2IRAK1JAK1JAK2JAK3MEN1OPRM1P2RX3PDE5ASCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASIGMAR1SLC6A2SYKTACR1TOP2ATYK2

The experimentally established mechanism targets of Citric 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
MEN1 known ✓ O00255 1/20 0.37
ESR2 known ✓ Q92731 1/20 0.36
TSHR P16473 1/20 0.43
MAPK10 P53779 1/20 0.43
PIK3CG P48736 2/20 0.41
CNR1 P21554 1/20 0.40
PARP1 P09874 2/20 0.38
PARP2 Q9UGN5 1/20 0.38
KMT2A Q03164 1/20 0.37
POLB P06746 2/20 0.37
KCNJ6 P48051 1/20 0.36
KCNJ5 P48544 1/20 0.36
KCNJ3 P48549 1/20 0.36
HTT P42858 1/20 0.36
CYP11B2 P19099 3/20 0.36
CYP11B1 P15538 2/20 0.36
BACE1 P56817 1/20 0.35
NAMPT P43490 1/20 0.35
ALDH1A1 P00352 2/20 0.35
KDM4E B2RXH2 1/20 0.35

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
Citric Acid SCHEMBL4339096 0.99 TSHR (0.44) TSHRMAPK10PIK3CGCNR1PARP1
Citric Acid SCHEMBL4327809 0.98 PIK3CG (0.41) TSHRMAPK10PIK3CGCNR1PARP1
SCHEMBL8231088 0.87 PIK3CG (0.49) TSHRMAPK10PIK3CGCNR1PARP1
SCHEMBL8230137 0.86 PIK3CG (0.48) TSHRMAPK10PIK3CGCNR1PARP1
SCHEMBL8237567 0.85 PIK3CG (0.49) TSHRMAPK10PIK3CGCNR1PARP1
Isopropyl Alcohol SCHEMBL4983070 0.84 PIK3CG (0.49) TSHRMAPK10PIK3CGCNR1PARP1
SCHEMBL4328277 0.83 PIK3CG (0.50) TSHRMAPK10PIK3CGCNR1PARP1
Isopropyl Alcohol SCHEMBL4984693 0.82 PIK3CG (0.50) TSHRMAPK10PIK3CGCNR1PARP1
Citric Acid SCHEMBL4336984 0.82 PIK3CG (0.47) PIK3CGCYP11B1
Citric Acid SCHEMBL4327392 0.82 PIK3CG (0.45) PIK3CGCYP11B2CYP11B1

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-20090149505-A1 Metabotropic Glutamate Receptor-Potentiating Isoindolones ASTRAZENECA AB (SE) 2009-06-11 US claimed
EP-1986998-A1 METABOTROPIC GLUTAMATE RECEPTOR-POTENTIATING SOINDOLONES AstraZeneca AB (SE) 2008-11-05 EP claimed
WO-2007095024-A1 METABOTROPIC GLUTAMATE RECEPTOR-POTENTIATING ΓSOINDOLONES ASTRAZENECA AB (SE) 2007-08-23 WO claimed
US-20090149505-A1 Metabotropic Glutamate Receptor-Potentiating Isoindolones ASTRAZENECA AB (SE) 2009-06-11 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-20090149505-A1 Metabotropic Glutamate Receptor-Potentiating Isoindolones GRM1, GRIN1, GRM3 MEN1 3491/4885ESR2 370/4885TSHR 290/4885

“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.