Triclofos

Triclofos

SCHEMBL122124

O=P(O)(O)OCC(Cl)(Cl)Cl.[NaH]

nearest known ligand 0.37

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQ

The experimentally established mechanism targets of Triclofos. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
FBP1 P09467 1/20 0.37
TPI1 P60174 2/20 0.34
LPAR3 Q9UBY5 4/20 0.33
LPAR2 Q9HBW0 3/20 0.33
LPAR1 Q92633 2/20 0.33
PGK1 P00558 1/20 0.33
PGK2 P07205 1/20 0.33
FDPS P14324 1/20 0.32
BLM P54132 1/20 0.32
TDP1 Q9NUW8 1/20 0.32
PGD P52209 2/20 0.31
MPI P34949 1/20 0.31
KDM4E B2RXH2 1/20 0.31
CYP2C19 P33261 1/20 0.31
KMT2A Q03164 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
Triclofos SCHEMBL125854 0.97 FBP1 (0.38) FBP1TPI1LPAR3LPAR2LPAR1
Triclofos SCHEMBL27912874 0.86 S1PR1 (0.33) FBP1TPI1
SCHEMBL3176347 0.81 TSHR (0.33) KDM4ECYP2C19KMT2A
Triclofos SCHEMBL28702793 0.81 FBP1 (0.33) FBP1LPAR3LPAR2LPAR1
Triclofos SCHEMBL10494633 0.81 FDPS (0.37) PGK1PGK2FDPSTDP1
Triclofos SCHEMBL16824084 0.80 LPAR3 (0.46) LPAR3LPAR2LPAR1
SCHEMBL4995915 0.79 KDM4E (0.31) TDP1KDM4ECYP2C19KMT2A
SCHEMBL31114338 0.79 PGK1 (0.38) FBP1TPI1LPAR3LPAR2LPAR1
SCHEMBL27754463 0.78 FDPS (0.39) FDPSBLMTDP1
Triclofos SCHEMBL10665197 0.78 TRIM24 (0.39)

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 518 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20200187851-A1 PERIODONTAL DISEASE STRATIFICATION AND USES THEREOF THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL 2020-06-18 US claimed
US-8268352-B2 Modified release composition for highly soluble drugs TORRENT PHARMACEUTICALS LIMITED (IN) 2012-09-18 US claimed
US-8263125-B2 Dosage form for high dose-high solubility active ingredients that provides for immediate release and modified release of the active ingredients TORRENT PHARMACEUTICALS LIMITED (IN) 2012-09-11 US claimed
EP-1273301-B1 Pharmaceutical preparations based on active ingredients susceptible to illicit administration ALTERGON SA (CH) 2006-09-06 EP claimed
US-20060024365-A1 Novel dosage form VAYA NAVIN 2006-02-02 US claimed
US-20060018933-A1 Novel drug delivery system TORRENT PHARMACEUTICALS LIMITED (IN) 2006-01-26 US claimed
US-20060018934-A1 Novel drug delivery system TORRENT PHARMACEUTICALS LIMITED (IN) 2006-01-26 US claimed
US-20060014697-A1 Pharmaceutical compositions for prevention of overdose or abuse SHIRE LLC 2006-01-19 US claimed
US-20040058946-A1 Abuse-resistant prodrugs of oxycodone and other pharmaceuticals COLLEGIUM PHARMACEUTICAL, INC. 2004-03-25 US claimed
EP-1273301-A2 Pharmaceutical preparations based on active ingredients susceptible to illicit administration ALTERGON S.A. (CH) 2003-01-08 EP claimed
US-5811547-A Method for inducing crystalline state transition in medicinal substance NIPPON SHINYAJU CO., LTD. (JP) 1998-09-22 US claimed
JP-8301312-A None JP disclosed
EP-4706683-A2 CHEWABLE FORMULATIONS Elanco Tiergesundheit AG (CH) 2026-03-11 EP disclosed
US-20260034059-A1 ORAL FILM COMPOSITIONS AND DOSAGE FORMS HAVING PRECISE ACTIVE DISSOLUTION PROFILES AQUESTIVE THERAPEUTICS, INC. (US) 2026-02-05 US disclosed
US-12465564-B2 Oral and nasal compositions and methods of treatment AQUESTIVE THERAPEUTICS, INC. (US) 2025-11-11 US disclosed
EP-0472969-A1 External preparation comprising calcium silicate Eisai Co., Ltd. (JP) 1992-03-04 EP disclosed
EP-0388954-A2 Freeze-dried polymer dispersions and the use thereof in preparing sustained-release pharmaceutical compositions FMC Corporation (US) 1990-09-26 EP disclosed
EP-0182765-A2 Electrochemical controlled release drug delivery system THE REGENTS OF THE UNIVERSITY OF MINNESOTA (US) 1986-05-28 EP disclosed
US-4585652-A REDOX SITES ON CHARGED POLYMER REGENTS OF THE UNIVERSITY OF MINNESOTA (US) 1986-04-29 US disclosed
US-4423038-A Phosphoryl compounds, pharmaceutical preparations containing such compounds, and their use CIBA-GEIGY CORPORATION (US) 1983-12-27 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 (2 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-20040058946-A1 Abuse-resistant prodrugs of oxycodone and other pharmaceuticals OPRK1, OPRM1, OPRL1 FBP1 2233/4885TPI1 2281/4885LPAR3 1591/4885
US-20260034059-A1 ORAL FILM COMPOSITIONS AND DOSAGE FORMS HAVING PRECISE ACTIVE DISSOLUTION PROFILES SORD, SLC6A13, CACNA1A FBP1 3888/4885TPI1 3191/4885LPAR3 4818/4885

“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.