Citric Acid

Citric Acid

SCHEMBL9439612

CCCCCCCCCCCCN(C)C.O=C(O)CC(O)(CC(=O)O)C(=O)O

nearest known ligand 0.52

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 2/20 0.44
ESR1 known ✓ P03372 1/20 0.41
ESR2 known ✓ Q92731 1/20 0.41
DNM1 Q05193 5/20 0.52
ALDH1A1 P00352 3/20 0.52
LMNA P02545 5/20 0.44
KDM4E B2RXH2 4/20 0.44
CYP1A2 P05177 2/20 0.44
CYP2D6 P10635 2/20 0.44
KMT2A Q03164 2/20 0.44
BLM P54132 2/20 0.44
HSPD1 P10809 1/20 0.44
HSPE1 P61604 1/20 0.44
TSHR P16473 2/20 0.41
GMNN O75496 1/20 0.41
TP53 P04637 1/20 0.41
CYP3A4 P08684 1/20 0.41
CYP2C9 P11712 1/20 0.41
ALOX12 P18054 1/20 0.41
NFKB1 P19838 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 SCHEMBL29600959 1.00 DNM1 (0.52) DNM1ALDH1A1LMNAKDM4EMEN1
Citric Acid SCHEMBL29600140 1.00 DNM1 (0.52) DNM1ALDH1A1LMNAKDM4EMEN1
Citric Acid SCHEMBL21219853 1.00 DNM1 (0.52) DNM1ALDH1A1LMNAKDM4EMEN1
Citric Acid SCHEMBL10888651 1.00 DNM1 (0.52) DNM1ALDH1A1LMNAKDM4EMEN1
Citric Acid SCHEMBL29562281 1.00 DNM1 (0.52) DNM1ALDH1A1LMNAKDM4EMEN1
Citric Acid SCHEMBL9814769 1.00 DNM1 (0.52) DNM1ALDH1A1LMNAKDM4EMEN1
Citric Acid SCHEMBL22556290 0.88 ALDH1A1 (0.54) ALDH1A1LMNAKDM4EMEN1CYP1A2
Citric Acid SCHEMBL10687560 0.87 ALDH1A1 (0.68) ALDH1A1MEN1KMT2ABLMHSPD1
Citric Acid SCHEMBL875432 0.87 ALDH1A1 (0.68) ALDH1A1MEN1KMT2ABLMHSPD1
Citric Acid SCHEMBL27042357 0.87 ALDH1A1 (0.68) ALDH1A1MEN1KMT2ABLMHSPD1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5356896-A Alkaline stabiling medium SANDOZ LTD. (CH) 1994-10-18 US disclosed
US-5296627-A Substituted butylene oxide-ethylene oxide copolymers PPG INDUSTRIES, INC. (US) 1994-03-22 US disclosed
US-5162475-A Copolymers with ethylenically unsaturated monomers; shrinkage inhibition of knit or non-woven fabrics PPG INDUSTRIES, INC. (US) 1992-11-10 US disclosed
EP-0422120-A4 POLYMERIZABLE SURFACTANT 1991-08-21 EP disclosed
EP-0422120-A1 POLYMERIZABLE SURFACTANT PPG INDUSTRIES, INC. (US) 1991-04-17 EP disclosed
WO-1989012618-A1 POLYMERIZABLE SURFACTANT PPG INDUSTRIES, INC. (US) 1989-12-28 WO disclosed
EP-0096103-B1 PROCESS FOR MAKING IONIC STRUCTURED PARTICLE LATEXES USING REACTIVE POLYMERIC SURFACTANTS THE DOW CHEMICAL COMPANY (US) 1987-12-23 EP disclosed
EP-0096103-A2 Process for making ionic structured particle latexes using reactive polymeric surfactants THE DOW CHEMICAL COMPANY (US) 1983-12-21 EP disclosed
US-4337185-A WHEREIN IONS ARE CHEMICALLY BOUND ON SURFACES OF POLYMER PARTICLES THE DOW CHEMICAL COMPANY (US) 1982-06-29 US disclosed
US-4113710-A EMULSION POLYMERIZATION THE DOW CHEMICAL COMPANY (US) 1978-09-12 US disclosed
US-4056501-A COPOLYMER THE DOW CHEMICAL COMPANY (US) 1977-11-01 US disclosed
US-4017372-A Process for electrodeposition of cross-linked polymer coatings THE DOW CHEMICAL COMPANY (US) 1977-04-12 US disclosed
US-4017442-A Structured-particle latexes THE DOW CHEMICAL COMPANY (US) 1977-04-12 US disclosed