SCHEMBL7534555

SCHEMBL7534555

CCCCC(CC)C(OCC)OCC

nearest known ligand 0.34

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.34
TDP1 Q9NUW8 1/20 0.34
CA2 P00918 4/20 0.33
CYP3A4 P08684 3/20 0.33
TSHR P16473 2/20 0.33
DNM1 Q05193 2/20 0.33
CA1 P00915 2/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
THRB P10828 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.32
MAPK1 P28482 1/20 0.32
OPRM1 P35372 1/20 0.32
LMNA P02545 1/20 0.32

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
SCHEMBL28181475 0.90 ALDH1A1 (0.33) ALDH1A1CA2TSHRCA1MAPK1
Tetradecylamine SCHEMBL27594554 0.87 DNM1 (0.46) ALDH1A1TDP1CYP3A4TSHRDNM1
SCHEMBL27467883 0.86
SCHEMBL16541773 0.85 THRB (0.36) THRBLMNA
SCHEMBL7526143 0.84 ALDH1A1 (0.33) ALDH1A1TDP1CA2CYP3A4TSHR
SCHEMBL7530675 0.84 CYP3A4 (0.33) ALDH1A1TDP1CA2CYP3A4TSHR
SCHEMBL7526349 0.82 DNM1 (0.41) ALDH1A1TDP1CA2CYP3A4DNM1
Ammonia Solution, Strong SCHEMBL28111996 0.82 CYP3A4 (0.32) ALDH1A1TDP1CA2CYP3A4TSHR
SCHEMBL11176471 0.82 THRB (0.31) THRB
SCHEMBL11185988 0.82 LMNA (0.31) ALDH1A1THRBLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5354911-A From diacetals; catalyst composed of acid and amine HOECHST AKTIENGESELLSCHAFT (DE) 1994-10-11 US claimed
CN-107743484-A The amphyl for the treatment of cancer 麦地那创新药物研究中心基金会 2018-02-27 CN disclosed
CN-107488172-A A kind of preparation method of Afatinib 山东新时代药业有限公司 2017-12-19 CN disclosed
CN-106187904-A 2-phenylimidazole analog derivative containing propioloyl amido and preparation method thereof and pharmaceutical composition and purposes 中国医学科学院药物研究所 2016-12-07 CN disclosed
EP-0993431-B1 METHOD FOR PRODUCING ENOL ETHERS BASF AG (DE) 2002-03-27 EP disclosed
US-6211416-B1 REACTING ACETAL OR KETAL WITH ACETYLENE OR ALLENE IN GAS PHASE IN PRESENCE OF CATALYST SELECTED FROM ZINC- OR CADMIUM-SILICON- AND OXYGEN-CONTAINING HETEROGENEOUS CATALYST BASF AKTIENGESELLSCHAFT (DE) 2001-04-03 US disclosed
EP-0993431-A1 METHOD FOR PRODUCING ENOL ETHERS BASF AKTIENGESELLSCHAFT (DE) 2000-04-19 EP disclosed
EP-0703211-B1 Process for the preparation of unsaturated ethers DEGUSSA (DE) 1999-11-10 EP disclosed
US-5869418-A COMPOSED OF A TITANIUM COMPOUND, AN ORGANOALUMINUM COCATALYST AND A FIRST AND SECOND EXTERNAL ELECTRON DONOR, WHEREIN FIRST ELECTRON DONOR IS AN ACETAL DERIVATIVE OF AN ALDEHYDE BOREALIS HOLDING A/S (DK) 1999-02-09 US disclosed
WO-1998058894-A1 METHOD FOR PRODUCING ENOL ETHERS BASF AKTIENGESELLSCHAFT (DE) 1998-12-30 WO disclosed
US-5576465-A DEHYDROETHERIFICATION OF ACETALS OR KETALS BY HEATING HUELS AKTIENGESELLSCHAFT (DE) 1996-11-19 US disclosed
EP-0703211-A1 Process for the preparation of unsaturated ethers HÜLS AKTIENGESELLSCHAFT (DE) 1996-03-27 EP disclosed
EP-0490221-B1 Method for the production of unsaturated ethers HOECHST AG (DE) 1995-08-09 EP disclosed
US-5354911-A From diacetals; catalyst composed of acid and amine HOECHST AKTIENGESELLSCHAFT (DE) 1994-10-11 US disclosed
EP-0490221-A2 Method for the production of unsaturated ethers HOECHST AKTIENGESELLSCHAFT (DE) 1992-06-17 EP disclosed
US-4247611-A ACETAL RESIN, ACID DONER HOECHST AKTIENGESELLSCHAFT (DE) 1981-01-27 US disclosed