SCHEMBL8909436

SCHEMBL8909436

COC(C)(CCCC(C)CCCC(C)C)OC

nearest known ligand 0.52

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.52
CYP3A4 P08684 2/20 0.52
MEN1 O00255 1/20 0.52
ALOX15 P16050 1/20 0.52
KMT2A Q03164 1/20 0.52
BLM P54132 1/20 0.44
PTPN1 P18031 3/20 0.40
PTPN2 P17706 1/20 0.40
CDC25B P30305 1/20 0.40
ALDH1A1 P00352 1/20 0.31
TDP1 Q9NUW8 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
SCHEMBL8909426 1.00 LMNA (0.52) LMNACYP3A4MEN1ALOX15KMT2A
SCHEMBL17885433 1.00 LMNA (0.52) LMNACYP3A4MEN1ALOX15KMT2A
SCHEMBL15822080 1.00 LMNA (0.52) LMNACYP3A4MEN1ALOX15KMT2A
SCHEMBL15825970 1.00 LMNA (0.52) LMNACYP3A4MEN1ALOX15KMT2A
SCHEMBL17268254 1.00 LMNA (0.52) LMNACYP3A4MEN1ALOX15KMT2A
SCHEMBL18697210 0.83 LMNA (0.52) LMNACYP3A4MEN1ALOX15KMT2A
SCHEMBL21180973 0.83 LMNA (0.52) LMNACYP3A4MEN1ALOX15KMT2A
SCHEMBL10834300 0.83 LMNA (0.52) LMNACYP3A4MEN1ALOX15KMT2A
SCHEMBL17885434 0.83 LMNA (0.52) LMNACYP3A4MEN1ALOX15KMT2A
SCHEMBL2400702 0.81 TSHR (0.41) LMNACYP3A4MEN1ALOX15KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2935177-B1 (6R,10R)-6,10,14-TRIMETYLPENTADECAN-2-ONE PREPARED FROM 6,10-DIMETYLUNDEC-5-EN-2-ONE OR 6,10-DIMETYLUNDECA-5,9-DIEN-2-ONE DSM IP ASSETS BV (NL) 2019-07-24 EP disclosed
EP-2935189-B1 USING MIXTURES OF E/Z ISOMERS TO OBTAIN QUANTITATIVELY SPECIFIC PRODUCTS BY COMBINING ASYMMETRIC HYDROGENATION AND ISOMERIZATION DSM IP ASSETS BV (NL) 2019-06-12 EP disclosed
EP-2935233-B1 PROCESS OF ASYMMETRIC HYDROGENATION OF KETALS AND ACETALS DSM IP ASSETS BV (NL) 2019-01-30 EP disclosed
EP-2935188-B1 USING MIXTURES OF E/Z ISOMERS TO OBTAIN QUANTITATIVELY SPECIFIC PRODUCTS BY COMBINED ASYMMETRIC HYDROGENATIONS DSM IP ASSETS BV (NL) 2018-08-01 EP disclosed
CN-104918909-B Specific product is quantitatively obtained by the asymmetric hydrogenation of combination using the mixture of E/Z isomers 帝斯曼知识产权资产管理有限公司 2018-05-11 CN disclosed
CN-104854069-B (6R,10R) -6,10, 14-trimethylpentadecan-2-one prepared from 6, 10-dimethylundec-5-en-2-one or 6, 10-dimethylundec-5, 9-dien-2-one 帝斯曼知识产权资产管理有限公司 2017-06-20 CN disclosed
US-9573872-B2 Using mixtures of E/Z isomers to obtain quantitatively specific products by combining asymmetric hydrogenation and isomerization DSM IP ASSETS B.V. (NL) 2017-02-21 US disclosed
US-9561989-B2 Process of asymmetric hydrogenation of ketals and acetals DSM IP ASSETS B.V. (NL) 2017-02-07 US disclosed
US-9458076-B2 Using mixtures of E/Z isomers to obtain quantitatively specific products by combined asymmetric hydrogenations DSM IP ASSETS B.V. (NL) 2016-10-04 US disclosed
US-9452961-B2 (6R,10R)-6,10,14-trimetylpentadecan-2-one prepared from 6,10-dimetylundec-5-en-2-one or 6,10-dimetylundeca-5,9-dien-2-one DSM IP ASSETS B.V. (NL) 2016-09-27 US disclosed
US-20150329457-A1 (6R,10R)-6,10,14-TRIMETYLPENTADECAN-2-ONE PREPARED FROM 6,10-DIMETYLUNDEC-5-EN-2-ONE OR 6,10-DIMETYLUNDECA-5,9-DIEN-2-ONE DSM IP ASSETS B.V. (NL) 2015-11-19 US disclosed
US-20150329457-A1 (6R,10R)-6,10,14-TRIMETYLPENTADECAN-2-ONE PREPARED FROM 6,10-DIMETYLUNDEC-5-EN-2-ONE OR 6,10-DIMETYLUNDECA-5,9-DIEN-2-ONE DSM IP ASSETS B.V. (NL) 2015-11-19 US disclosed
US-20150321986-A1 USING MIXTURES OF E/Z ISOMERS TO OBTAIN QUANTITATIVELY SPECIFIC PRODUCTS BY COMBINED ASYMMETRIC HYDROGENATIONS DSM IP ASSETS B.V. (NL) 2015-11-12 US disclosed
EP-2935233-A1 PROCESS OF ASYMMETRIC HYDROGENATION OF KETALS AND ACETALS DSM IP Assets B.V. (NL) 2015-10-28 EP disclosed
CN-104918909-A Using mixtures of E/Z isomers to obtain quantitatively specific products by combined asymmetric hydrogenations DSM IP ASSETS BV 2015-09-16 CN disclosed
CN-104884446-A Asymmetric Hydrogenation of Ketals and Acetals DSM IP ASSETS BV 2015-09-02 CN disclosed
CN-104884420-A USING MIXTURES OF E/Z ISOMERS TO OBTAIN QUANTITATIVELY SPECIFIC PRODUCTS BY COMBINING ASYMMETRIC HYDROGENATION AND ISOMERIZATION DSM IP ASSETS BV 2015-09-02 CN disclosed
CN-104854069-A (6R,10R) -6,10, 14-trimethylpentadecan-2-one prepared from 6, 10-dimethylundec-5-en-2-one or 6, 10-dimethylundec-5, 9-dien-2-one DSM IP ASSETS BV 2015-08-19 CN disclosed
WO-2014096096-A1 PROCESS OF ASYMMETRIC HYDROGENATION OF KETALS AND ACETALS DSM IP ASSETS B.V. (NL) 2014-06-26 WO disclosed
US-5600015-A USING RUTHENIUM COMPLEX OF OPTICALLY ACTIVE ATROPISOMERIC DIPHOSPHINE LIGAND AS HYDROGENATION CATALYST HOFFMANN-LA ROCHE INC. (US) 1997-02-04 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-20150321986-A1 USING MIXTURES OF E/Z ISOMERS TO OBTAIN QUANTITATIVELY SPECIFIC PRODUCTS BY COMBINED ASYMMETRIC HYDROGENATIONS EPHX2, HBZ, ELOVL5 LMNA 681/4885CYP3A4 247/4885MEN1 1465/4885
US-20150329457-A1 (6R,10R)-6,10,14-TRIMETYLPENTADECAN-2-ONE PREPARED FROM 6,10-DIMETYLUNDEC-5-EN-2-ONE OR 6,10-DIMETYLUNDECA-5,9-DIEN-2-ONE PDE12, CYP2D6, PDE9A LMNA 1447/4885CYP3A4 111/4885MEN1 1634/4885

“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.