SCHEMBL6769239

SCHEMBL6769239

CCc1cccc(CC)c1NC(=O)CCl

nearest known ligand 0.59

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 0.59
ALOX15 P16050 1/20 0.58
TSHR P16473 1/20 0.58
CYP2C19 P33261 1/20 0.58
HIF1A Q16665 1/20 0.58
TDP1 Q9NUW8 1/20 0.58
ALDH1A1 P00352 6/20 0.54
LMNA P02545 2/20 0.54
MAPT P10636 2/20 0.54
HPGD P15428 1/20 0.54
THRB P10828 1/20 0.49
CACNA1C Q13936 2/20 0.49
SCN5A Q14524 2/20 0.49
KDM4E B2RXH2 2/20 0.49
NLRP3 Q96P20 1/20 0.49
TP53 P04637 1/20 0.48
POLB P06746 1/20 0.48

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
SCHEMBL27877978 0.92 SMN1; SMN2 (0.51) SMN1; SMN2ALOX15TSHRCYP2C19HIF1A
SCHEMBL6546027 0.90 POLB (0.61) SMN1; SMN2ALOX15TDP1ALDH1A1LMNA
SCHEMBL30323772 0.90 POLB (0.61) SMN1; SMN2ALOX15TDP1ALDH1A1LMNA
SCHEMBL7223947 0.85 SMN1; SMN2 (0.49) SMN1; SMN2ALOX15TSHRCYP2C19HIF1A
SCHEMBL28264607 0.85 ALOX15 (0.55) ALOX15TSHRCYP2C19HIF1ATDP1
SCHEMBL10668835 0.84 SMN1; SMN2 (0.48) SMN1; SMN2ALOX15TSHRCYP2C19HIF1A
SCHEMBL10588657 0.84 ALOX15 (0.62) ALOX15TSHRCYP2C19HIF1ATDP1
SCHEMBL10891813 0.83 SMN1; SMN2 (0.61) SMN1; SMN2ALOX15TSHRCYP2C19HIF1A
SCHEMBL21820780 0.82 CYP2C19 (0.60) ALOX15TSHRCYP2C19HIF1ATDP1
SCHEMBL23388356 0.81 CYP2C19 (0.58) ALOX15TSHRCYP2C19HIF1ATDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110862308-A Preparation method and application of formaldehyde alcohol solution 湖北泰盛化工有限公司 2020-03-06 CN claimed
CN-1391439-A Synergistic herbicidal active substance combinations BAYER AG (DE) 2003-01-15 CN claimed
CN-1378424-A Selective herbicides on basis of n-aryl-trizoline (thio) ones BAYER AG (DE) 2002-11-06 CN claimed
CN-110612119-B Phosphatidylether (PLE) CAR T cell tumor targeting (CTCT) agents 西雅图儿童医院(DBA西雅图儿童研究所) 2024-10-29 CN disclosed
US-20240226160-A9 ACTIVITY-INDUCIBLE FUSION PROTEINS HAVING A HEAT SHOCK PROTEIN 90 BINDING DOMAIN SEATTLE CHILDREN'S HOSPITAL D/B/A SEATTLE CHILDREN'S RESEARCH INSTITUTE (US) 2024-07-11 US disclosed
US-20240131072-A1 ACTIVITY-INDUCIBLE FUSION PROTEINS HAVING A HEAT SHOCK PROTEIN 90 BINDING DOMAIN SEATTLE CHILDREN'S HOSPITAL D/B/A SEATTLE CHILDREN'S RESEARCH INSTITUTE (US) 2024-04-25 US disclosed
EP-4291571-A2 ACTIVITY-INDUCIBLE FUSION PROTEINS HAVING A HEAT SHOCK PROTEIN 90 BINDING DOMAIN Seattle Children's Hospital d/b/a Seattle Children's Research Institute (US) 2023-12-20 EP disclosed
US-20230322925-A1 PHOSPHOLIPID ETHER (PLE) CAR T CELL TUMOR TARGETING (CTCT) AGENTS SEATTLE CHILDREN’S HOSPITAL DBA SEATTLE CHILDREN’S RES INSTITUTE (US) 2023-10-12 US disclosed
US-20230172981-A1 METHODS AND COMPOSITIONS FOR STIMULATION OF CHIMERIC ANTIGEN RECEPTOR T CELLS WITH HAPTEN LABELLED CELLS SEATTLE CHILDRENS HOSPITAL DBA SEATTLE CHILDRENS RES INST (US) 2023-06-08 US disclosed
US-11649288-B2 Phospholipid ether (PLE) CAR T cell tumor targeting (CTCT) agents SEATTLE CHILDREN'S HOSPITAL (US) 2023-05-16 US disclosed
CN-114920418-A Resource recovery method for amide pesticide production wastewater and application thereof 南通江山农药化工股份有限公司 2022-08-19 CN disclosed
US-4371717-A ETHERIFICATION, ALDEHYDES MONSANTO COMPANY (US) 1983-02-01 US disclosed
EP-0066106-A1 New phenoxybenzoates, process for preparing these compounds, compositions containing them and method of use GAF CORPORATION (US) 1982-12-08 EP disclosed
US-4319917-A N-(2-Cyanoalkoxy)methyl-N-(2-,3-, or 6-alkylphenyl)-α-haloacetamides PPG INDUSTRIES, INC. (US) 1982-03-16 US disclosed
EP-0037656-A1 A process for the in-solvent, in-situ generation of N-substituted-2-haloacetanilides MONSANTO COMPANY (US) 1981-10-14 EP disclosed
US-4284564-A Process for the in-solvent, in-situ generation of haloalkyl alkyl ethers useful to produce N-substituted-2-haloacetanilides MONSANTO COMPANY (US) 1981-08-18 US disclosed
US-4258196-A REACTING THE ANION OF A PRIMARY OR SECONDARY 2-HALOACETAMIDE WITH AN ALKYLATING AGENT MONSANTO COMPANY (US) 1981-03-24 US disclosed
US-4237068-A Primary aminoacylanilides ASTRA PHARMACEUTICAL PRODUCTS, INC. (US) 1980-12-02 US disclosed
US-4218477-A LONG LASTING ORAL AGENTS ASTRA PHARMACEUTICAL PRODUCTS, INC. (US) 1980-08-19 US disclosed
US-4178383-A Fungicidally active oxime-ethers of isonitrosocyanoacetamides BAYER AKTIENGESELLSCHAFT (DE) 1979-12-11 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-11649288-B2 Phospholipid ether (PLE) CAR T cell tumor targeting (CTCT) agents PHOSPHO1, LCAT, CD47 SMN1; SMN2 1861/4885ALOX15 700/4885TSHR 1224/4885
US-20230322925-A1 PHOSPHOLIPID ETHER (PLE) CAR T CELL TUMOR TARGETING (CTCT) AGENTS PHOSPHO1, LCAT, CD47 SMN1; SMN2 1861/4885ALOX15 700/4885TSHR 1224/4885

“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.