SCHEMBL8200504

SCHEMBL8200504

CCCCCCCCCCCCCCCC[P]1(O)OCCO1

nearest known ligand 0.38

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.38
THRB P10828 1/20 0.38
ALDH1A1 P00352 3/20 0.36
LMNA P02545 2/20 0.36
HSD17B10 Q99714 1/20 0.36
MEN1 O00255 1/20 0.36
KMT2A Q03164 1/20 0.36
EPHX1 P07099 1/20 0.35
HSP90AA1 P07900 1/20 0.32
CES2 O00748 3/20 0.32
CES1 P23141 3/20 0.32
SMN1; SMN2 Q16637 1/20 0.32
SLC22A6 Q4U2R8 1/20 0.31
SLC22A8 Q8TCC7 1/20 0.31
GPR84 Q9NQS5 1/20 0.31
PPARG P37231 1/20 0.31
PPARD Q03181 1/20 0.31
PPARA Q07869 1/20 0.31

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
SCHEMBL9249189 0.71 RAD52 (0.32) TSHRTHRBEPHX1
Oxirane SCHEMBL28319014 0.67 TSHR (0.61) TSHRTHRBALDH1A1LMNAHSD17B10
Oxirane SCHEMBL28436205 0.67 TSHR (0.61) TSHRTHRBALDH1A1LMNAHSD17B10
Oxirane SCHEMBL28247935 0.67 TSHR (0.61) TSHRTHRBALDH1A1LMNAHSD17B10
Heptane SCHEMBL11316948 0.67 TSHR (0.61) TSHRTHRBALDH1A1LMNAHSD17B10
Decane SCHEMBL25391362 0.66 TSHR (0.89) TSHRTHRBALDH1A1LMNAHSD17B10
Dodecane SCHEMBL29078900 0.66 TSHR (0.89) TSHRTHRBALDH1A1LMNAHSD17B10
Hexadecane SCHEMBL18784651 0.66 TSHR (0.89) TSHRTHRBALDH1A1LMNAHSD17B10
Fluoride SCHEMBL28664164 0.66 TSHR (0.89) TSHRTHRBALDH1A1LMNAHSD17B10
Octane SCHEMBL28508043 0.66 TSHR (0.89) TSHRTHRBALDH1A1LMNAHSD17B10

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-6028209-A REACTING A FATTY ALCOHOL WITH PHOSPHORUS OXYCHLORIDE IN A SINGLE VESSEL PROCESS, THEN REACTING WITH CHOLINE SALT TO FORM PHOSPHORIC ACID DIESTER CHLORIDE, HYDROLYSIS AND ISOLATION ASTA MEDICA AG (DE) 2000-02-22 US disclosed
US-5942639-A REACTING A C14-C18 N-ALKANOL WITH PHOSPHORUS OXYCHLORIDE THEN REACTING THE PRODUCT WITHOUT ISOLATION OR PURIFICATION WITH A CHOLINE SALT IN THE PRESENCE OF A BASE TO FORM THE PHOSPHORIC ACID DIESTER CHLORIDE, HYDROLYSING; MIXED BED ION EXCHANGING ASTA MEDICA AKTIENGESELLSCHAFT (DE) 1999-08-24 US disclosed
CN-1034941-C Process for preparing alkylphosphocholines and production thereof in pure form ASTA MEDICA AG (DE) 1997-05-21 CN disclosed
CN-1068331-A The production of the preparation method of phosphocholine alkyl ester and their pure form ASTA MEDICA AG (DE) 1993-01-27 CN disclosed