Citric Acid

Citric Acid

SCHEMBL432573

O=C(O)CC(O)(CC(=O)O)C(=O)O.O=C(O)CC(O)(CC(=O)O)C(=O)O.[Ca]

nearest known ligand 0.94

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 19)

geneUniProtsupporting neighboursconfidence
MEN1 known ✓ O00255 1/20 0.41
ALDH1A1 P00352 2/20 0.94
HMGCR P04035 1/20 0.48
CHRM1 P11229 1/20 0.48
TBXA2R P21731 1/20 0.48
ADRA1A P35348 1/20 0.48
TSHR P16473 2/20 0.46
CYP2D6 P10635 2/20 0.46
CYP2C19 P33261 1/20 0.46
HIF1A Q16665 1/20 0.46
ACLY P53396 4/20 0.44
KDM4E B2RXH2 2/20 0.43
LMNA P02545 2/20 0.43
MAPT P10636 1/20 0.43
ALOX15 P16050 1/20 0.43
SLC13A5 Q86YT5 4/20 0.42
CPT2 P23786 1/20 0.42
CYP1A2 P05177 1/20 0.41
KMT2A Q03164 1/20 0.41

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 SCHEMBL9361094 1.00 ALDH1A1 (0.94) ALDH1A1HMGCRCHRM1TBXA2RADRA1A
Citric Acid SCHEMBL29486777 1.00 ALDH1A1 (0.94) ALDH1A1HMGCRCHRM1TBXA2RADRA1A
Citric Acid SCHEMBL29369759 0.97 ALDH1A1 (0.88) ALDH1A1HMGCRCHRM1TBXA2RADRA1A
Citric Acid SCHEMBL5269305 0.97 ALDH1A1 (0.88) ALDH1A1HMGCRCHRM1TBXA2RADRA1A
Citric Acid SCHEMBL240402 0.97 ALDH1A1 (1.00) ALDH1A1HMGCRCHRM1TBXA2RADRA1A
Citric Acid SCHEMBL1331942 0.97 ALDH1A1 (1.00) ALDH1A1HMGCRCHRM1TBXA2RADRA1A
Citric Acid SCHEMBL3417188 0.97 ALDH1A1 (1.00) ALDH1A1HMGCRCHRM1TBXA2RADRA1A
Citric Acid SCHEMBL10896997 0.97 ALDH1A1 (1.00) ALDH1A1HMGCRCHRM1TBXA2RADRA1A
Citric Acid SCHEMBL842 0.97 ALDH1A1 (1.00) ALDH1A1HMGCRCHRM1TBXA2RADRA1A
Citric Acid SCHEMBL725546 0.97 ALDH1A1 (1.00) ALDH1A1HMGCRCHRM1TBXA2RADRA1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2595635-A1 POLYDEOXYRIBONUCLEOTIDES (PDRNS) FOR USE IN THE TREATMENT OF METABOLIC AND/OR LACTIC ACIDOSIS AND POLYDEOXYRIBONUCLEOTIDE-BASED COMPOSITIONS FOR THE AFORESAID USE Medestea Internazionale S.p.A. (IT) 2013-05-29 EP claimed
US-20130122091-A1 POLYDEOXYRIBONUCLEOTIDE-BASED COMPOSITIONS AND THEIR METHODS OF USE MEDESTEA INTERNAZIONALE SPA (IT) 2013-05-16 US claimed
WO-2012011063-A1 POLYDEOXYRIBONUCLEOTIDES (PDRNS) FOR USE IN THE TREATMENT OF METABOLIC AND/OR LACTIC ACIDOSIS AND POLYDEOXYRIBONUCLEOTIDE-BASED COMPOSITIONS FOR THE AFORESAID USE MEDESTEA INTERNAZIONALE S.P.A. (IT) 2012-01-26 WO claimed
US-20040224076-A1 Dietetic composition in the form of a salt substitute for table salt SANOFI-AVENTIS (FR) 2004-11-11 US claimed
EP-1051086-B1 DIETETIC COMPOSITION IN THE FORM OF A SUBSTITUTION SALT FOR TABLE SALT SANOFI SYNTHELABO (FR) 2002-04-17 EP claimed
EP-2595635-A1 POLYDEOXYRIBONUCLEOTIDES (PDRNS) FOR USE IN THE TREATMENT OF METABOLIC AND/OR LACTIC ACIDOSIS AND POLYDEOXYRIBONUCLEOTIDE-BASED COMPOSITIONS FOR THE AFORESAID USE Medestea Internazionale S.p.A. (IT) 2013-05-29 EP disclosed
US-20130122091-A1 POLYDEOXYRIBONUCLEOTIDE-BASED COMPOSITIONS AND THEIR METHODS OF USE MEDESTEA INTERNAZIONALE SPA (IT) 2013-05-16 US disclosed
WO-2012011063-A1 POLYDEOXYRIBONUCLEOTIDES (PDRNS) FOR USE IN THE TREATMENT OF METABOLIC AND/OR LACTIC ACIDOSIS AND POLYDEOXYRIBONUCLEOTIDE-BASED COMPOSITIONS FOR THE AFORESAID USE MEDESTEA INTERNAZIONALE S.P.A. (IT) 2012-01-26 WO disclosed
US-20040224076-A1 Dietetic composition in the form of a salt substitute for table salt SANOFI-AVENTIS (FR) 2004-11-11 US disclosed
US-4867942-A Process for the preparation of an effervescent granular material, effervescent granular material prepared by this process, as well as the use thereof GERGELY GERHARD (AT) 1989-09-19 US disclosed
EP-0298085-A1 ULTRADENSE AND MORE SOLUBLE AND BIOAVAILABLE PREPARATIONS OF CALCIUM CITRATE. UNIV TEXAS (US) 1989-01-11 EP disclosed
WO-1987005507-A1 ULTRADENSE AND MORE SOLUBLE AND BIOAVAILABLE PREPARATIONS OF CALCIUM CITRATE BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1987-09-24 WO disclosed