SCHEMBL1674941

SCHEMBL1674941

CN(C)C1CCCCCCCCCCC1

nearest known ligand 0.50

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
ADH1A P07327 8/20 0.50
ADH1C P00326 5/20 0.50
PHGDH O43175 2/20 0.44
FAAH O00519 1/20 0.44
MGLL Q99685 1/20 0.44
ADH1B P00325 1/20 0.39
HRH3 Q9Y5N1 3/20 0.38
HRH4 Q9H3N8 1/20 0.38
TDP1 Q9NUW8 1/20 0.36
ALDH1A1 P00352 2/20 0.35
KDM4E B2RXH2 1/20 0.35
MEN1 O00255 1/20 0.35
KMT2A Q03164 1/20 0.35
ADH4 P08319 1/20 0.35
HTR2A P28223 2/20 0.34
HTR2C P28335 2/20 0.34
HTR2B P41595 2/20 0.34

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
SCHEMBL15595 1.00
SCHEMBL1679002 1.00 ADH1A (0.50) ADH1AADH1CPHGDHFAAHMGLL
SCHEMBL612962 1.00 ADH1A (0.50) ADH1AADH1CPHGDHFAAHMGLL
SCHEMBL3080635 1.00
SCHEMBL283931 1.00 ADH1A (0.50) ADH1AADH1CPHGDHFAAHMGLL
SCHEMBL13356252 1.00 ADH1A (0.50) ADH1AADH1CPHGDHFAAHMGLL
SCHEMBL612785 1.00 ADH1A (0.50) ADH1AADH1CPHGDHFAAHMGLL
SCHEMBL28469806 1.00 ADH1A (0.50) ADH1AADH1CPHGDHFAAHMGLL
SCHEMBL20733112 1.00 ADH1A (0.50) ADH1AADH1CPHGDHFAAHMGLL
SCHEMBL28251831 1.00 ADH1A (0.50) ADH1AADH1CPHGDHFAAHMGLL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1056752-B1 Catalyst activators comprising expanded anions DOW GLOBAL TECHNOLOGIES INC (US) 2003-06-25 EP claimed
US-20250304543-A1 PROCESS FOR MAKING A SUBSTANTIALLY NITROSAMINE-FREE, SUBSTANTIALLY PEROXIDE-FREE, SUBSTANTIALLY COLORLESS AMINE OXIDE BASF SE (DE) 2025-10-02 US disclosed
EP-4536645-A1 PROCESS FOR MAKING A SUBSTANTIALLY NITROSAMINE-FREE, SUBSTANTIALLY PEROXIDE-FREE, SUBSTANTIALLY COLORLESS AMINE OXIDE BASF SE (DE) 2025-04-16 EP disclosed
CN-119365447-A Process for preparing substantially nitrosamine-free, peroxide-free, substantially colorless amine oxide 巴斯夫欧洲公司 2025-01-24 CN disclosed
WO-2023237729-A1 PROCESS FOR MAKING A SUBSTANTIALLY NITROSAMINE-FREE, SUBSTANTIALLY PEROXIDE-FREE, SUBSTANTIALLY COLORLESS AMINE OXIDE BASF SE (DE) 2023-12-14 WO disclosed
US-20230133581-A1 Novel 3,5-Diaminobenzoic Acid Compound, and PIN1 Inhibitor and Therapeutic Agent for Inflammatory Diseases Using Same HIROSHIMA UNIVERSITY (JP) 2023-05-04 US disclosed
US-10435375-B2 CXCR4 chemokine receptor modulators NORTHWESTERN UNIVERSITY (US) 2019-10-08 US disclosed
EP-1377613-B1 METHOD OF MAKING INTERPOLYMERS AND PRODUCTS MADE THEREFROM DOW GLOBAL TECHNOLOGIES LLC (US) 2019-06-19 EP disclosed
EP-1412398-B1 HIGH MELT STRENGTH POLYMERS AND METHOD OF MAKING SAME DOW GLOBAL TECHNOLOGIES LLC (US) 2019-04-24 EP disclosed
US-20180155295-A1 CXCR4 CHEMOKINE RECEPTOR MODULATORS NORTHWESTERN UNIVERSITY 2018-06-07 US disclosed
EP-0409043-A1 Reduction of nitrosamine formation SOLVAY INTEROX (US) 1991-01-23 EP disclosed
US-4960934-A Amine oxide process ETHYL CORPORATION (US) 1990-10-02 US disclosed
US-4942260-A REACTION OF A TERT-AMINE WITH HYDROGEN PEROXIDE IN THE PRESENCE OF CATALYTIC CARBON DIOXIDE ETHYL CORPORATION (US) 1990-07-17 US disclosed
EP-0356918-A1 Amine oxide process ETHYL CORPORATION (US) 1990-03-07 EP disclosed
US-4889954-A DIALKYLCARBONATE CATALYST ETHYL CORPORATION (US) 1989-12-26 US disclosed
EP-0320694-A2 Amine oxide process ETHYL CORPORATION (US) 1989-06-21 EP disclosed
EP-0307184-A2 Preparation of Amine Oxides ETHYL CORPORATION (US) 1989-03-15 EP disclosed
EP-0057362-B1 DIBENZOFURANE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS FUNGICIDES BASF Aktiengesellschaft (DE) 1984-06-20 EP disclosed
EP-0103277-A1 Quaternary ammonium salts of benzofuran derivatives and fungicides containing them BASF Aktiengesellschaft (DE) 1984-03-21 EP disclosed
US-4376776-A Dibenzofuran derivatives and their use for controlling fungi BASF AKTIENGESELLSCHAFT (DE) 1983-03-15 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 (3 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-10435375-B2 CXCR4 chemokine receptor modulators CXCR4, ACKR3, CXCR3 ADH1A 2418/4885ADH1C 3168/4885PHGDH 3868/4885
US-20230133581-A1 Novel 3,5-Diaminobenzoic Acid Compound, and PIN1 Inhibitor and Therapeutic Agent for Inflammatory Diseases Using Same PIN1, DUSP15, FKBP1A ADH1A 1528/4885ADH1C 1539/4885PHGDH 298/4885
US-20180155295-A1 CXCR4 CHEMOKINE RECEPTOR MODULATORS CXCR4, ACKR3, CXCR3 ADH1A 2418/4885ADH1C 3168/4885PHGDH 3868/4885

“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.