Choline

Choline

SCHEMBL4594631

C[N+](C)(C)CCO.NC(CS)C(=O)O

nearest known ligand 0.61

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADORA1ADORA2AADORA2BADORA3GNRHRMPLPDE3APDE3BPDE4APDE4BPDE4CPDE4DPPARASLC5A2

The experimentally established mechanism targets of Choline. 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
PTGS1 P23219 1/20 0.61
SLC7A11 Q9UPY5 1/20 0.61
MEN1 O00255 1/20 0.44
LMNA P02545 1/20 0.44
KMT2A Q03164 1/20 0.44
CYP3A4 P08684 1/20 0.44
SLC5A7 Q9GZV3 1/20 0.44
SLC7A5 Q01650 1/20 0.38
ENPEP Q07075 4/20 0.37
SLC1A1 P43005 4/20 0.35
SLC1A3 P43003 4/20 0.34
SLC1A2 P43004 4/20 0.34
GRIK1 P39086 3/20 0.33
GRIK2 Q13002 2/20 0.33
GRM8 O00222 1/20 0.33
GRM6 O15303 1/20 0.33
GRIN2D O15399 1/20 0.33
GRIN3B O60391 1/20 0.33
GSR P00390 1/20 0.33
CYP1A2 P05177 1/20 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
Choline SCHEMBL4594634 1.00 PTGS1 (0.61) PTGS1SLC7A11MEN1LMNAKMT2A
Choline SCHEMBL8135839 0.98 PTGS1 (0.59) PTGS1SLC7A11MEN1LMNAKMT2A
Choline SCHEMBL8135850 0.98 PTGS1 (0.59) PTGS1SLC7A11MEN1LMNAKMT2A
Choline SCHEMBL8135842 0.98 PTGS1 (0.59) PTGS1SLC7A11MEN1LMNAKMT2A
Cadaverine Tartrate SCHEMBL27758938 0.87 PTGS1 (0.47) PTGS1SLC7A11MEN1LMNAKMT2A
Choline SCHEMBL1683106 0.84 KMT2A (0.48) PTGS1SLC7A11MEN1LMNAKMT2A
Choline SCHEMBL1683101 0.84 KMT2A (0.48) PTGS1SLC7A11MEN1LMNAKMT2A
Cysteine SCHEMBL28102468 0.83 PTGS1 (0.80) PTGS1SLC7A11KMT2ASLC7A5ENPEP
Cysteine SCHEMBL28102471 0.83 PTGS1 (0.80) PTGS1SLC7A11KMT2ASLC7A5ENPEP
Choline SCHEMBL8217649 0.83 LMNA (0.43) PTGS1SLC7A11MEN1LMNAKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114621984-B Method for synthesizing 1, 5-pentanediamine by using ionic liquid to strengthen lysine decarboxylase 中国科学院过程工程研究所 2025-01-28 CN claimed
CN-114621984-A Method for synthesizing 1, 5-pentanediamine by strengthening lysine decarboxylase through ionic liquid 中国科学院过程工程研究所 2022-06-14 CN claimed
CN-114426992-A Amino functionalized ionic liquid reinforced CO2Biotransformation process 中国科学院过程工程研究所 2022-05-03 CN claimed
CN-114621984-B Method for synthesizing 1, 5-pentanediamine by using ionic liquid to strengthen lysine decarboxylase 中国科学院过程工程研究所 2025-01-28 CN disclosed
CN-114621984-A Method for synthesizing 1, 5-pentanediamine by strengthening lysine decarboxylase through ionic liquid 中国科学院过程工程研究所 2022-06-14 CN disclosed
CN-114426992-A Amino functionalized ionic liquid reinforced CO2Biotransformation process 中国科学院过程工程研究所 2022-05-03 CN disclosed
EP-1968650-A2 COMPOUNDS FOR DELIVERING AMINO ACIDS OR PEPTIDES WITH ANTIOXIDANT ACTIVITY INTO MITOCHONDRIA AND USE THEREOF University of Rochester (US) 2008-09-17 EP disclosed
WO-2007076323-A2 COMPOUNDS FOR DELIVERING AMINO ACIDS OR PEPTIDES WITH ANTIOXIDANT ACTIVITY INTO MITOCHONDRIA AND USE THEREOF UNIVERSITY OF ROCHESTER (US) 2007-07-05 WO disclosed