Citric Acid

Citric Acid

SCHEMBL6016965

COc1ccc(N(C)c2nc(NC3CCCCCC3)nc(NC3CCN(C)CC3)n2)cc1F.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
PDE5A known ✓ O76074 1/20 0.35
EHMT2 Q96KQ7 12/20 0.43
EHMT1 Q9H9B1 10/20 0.43
AURKA O14965 2/20 0.40
AURKB Q96GD4 1/20 0.40
BCL6 P41182 1/20 0.37
KDM1A O60341 1/20 0.37
RCOR1 Q9UKL0 1/20 0.37
WHR1 P49842 1/20 0.36
BRD4 O60885 1/20 0.36
CHEK1 O14757 1/20 0.36
IKBKB O14920 1/20 0.36
PAK4 O96013 1/20 0.36
CHEK2 O96017 1/20 0.36
ABL1 P00519 1/20 0.36
EGFR P00533 1/20 0.36
INSR P06213 1/20 0.36
LCK P06239 1/20 0.36
FGFR1 P11362 1/20 0.36
SELP P16109 1/20 0.36

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
SCHEMBL5457407 0.88 EHMT2 (0.53) EHMT2EHMT1AURKAAURKBBCL6
Citric Acid SCHEMBL4829665 0.85 EHMT2 (0.41) EHMT2EHMT1AURKAAURKBBCL6
SCHEMBL4837987 0.81 EHMT2 (0.50) EHMT2EHMT1AURKAAURKBBCL6
SCHEMBL5420636 0.80 EHMT2 (0.44) EHMT2EHMT1AURKAAURKBBCL6
SCHEMBL4837520 0.77 EHMT2 (0.49) EHMT2EHMT1KDM1ARCOR1MAPK1
Citric Acid SCHEMBL6017169 0.76 AURKA (0.38) EHMT2EHMT1AURKAAURKBCHEK1
Citric Acid SCHEMBL6865211 0.76 EHMT2 (0.37) EHMT2EHMT1
Malonic Acid SCHEMBL4829481 0.75 EHMT2 (0.45) EHMT2EHMT1AURKAAURKBBCL6
SCHEMBL4832215 0.75 EHMT2 (0.44) EHMT2EHMT1BCL6KDM4EALDH1A1
SCHEMBL4837222 0.75 CCR4 (0.43) EHMT2EHMT1AURKAAURKBBCL6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7112587-B2 Methods and compositions of novel triazine compounds REDDY US THERAPEUTICS, INC. (US) 2006-09-26 US disclosed
US-20040209881-A1 e.g., N-Cycloheptyl-N'(1-ethyl-pyrrolidin-2-ylmethyl)-6-(3-fluoro-4-methoxy-phenoxy)-[1,3,5]triazine-2,4-diamine; treating unwanted cellular proliferation, an inflammation mediated disease, or a hyperproliferative disease, or modulating a glycosidase enzyme DR. REDDY'S LABORATORIES LTD. (IN) 2004-10-21 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-20040209881-A1 e.g., N-Cycloheptyl-N'(1-ethyl-pyrrolidin-2-ylmethyl)-6-(3-fluoro-4-methoxy-phenoxy)-[1,3,5]triazine-2,4-diamine; treating unwanted cellular proliferation, an inflammation mediated disease, or a hyperproliferative disease, or modulating a glycosidase enzyme ENGASE, LIPG, GPI PDE5A 1095/4885EHMT2 2518/4885EHMT1 2850/4885

“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.