SCHEMBL2303261

SCHEMBL2303261

CCOC(=O)C(CC)C(C)C

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.43
LMNA P02545 1/20 0.42
HSD17B10 Q99714 1/20 0.42
ALOX15 P16050 1/20 0.40
MGAM O43451 1/20 0.40
GAA P10253 1/20 0.40
SI P14410 1/20 0.40
MGAM2 Q2M2H8 1/20 0.40
SOAT1 P35610 1/20 0.40
TRPA1 O75762 1/20 0.37
CA12 O43570 1/20 0.35
CA1 P00915 1/20 0.35
CA2 P00918 1/20 0.35
CA9 Q16790 1/20 0.35
PIN1 Q13526 1/20 0.34
HPGD P15428 1/20 0.34
MEN1 O00255 2/20 0.33
KMT2A Q03164 2/20 0.33
NPC1 O15118 1/20 0.33
CYP3A4 P08684 1/20 0.33

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
SCHEMBL17617141 1.00 ALDH1A1 (0.43) ALDH1A1LMNAHSD17B10ALOX15MGAM
SCHEMBL13575648 1.00 ALDH1A1 (0.43) ALDH1A1LMNAHSD17B10ALOX15MGAM
SCHEMBL235849 0.87 ALDH1A1 (0.50) ALDH1A1LMNAHSD17B10ALOX15MGAM
SCHEMBL13269547 0.84 ALDH1A1 (0.39) ALDH1A1LMNAHSD17B10ALOX15MGAM
SCHEMBL3700073 0.83 ALDH1A1 (0.42) ALDH1A1LMNAHSD17B10ALOX15MGAM
SCHEMBL638162 0.83 ALDH1A1 (0.42) ALDH1A1LMNAHSD17B10ALOX15MGAM
SCHEMBL12868877 0.83 ALDH1A1 (0.42) ALDH1A1LMNAHSD17B10ALOX15MGAM
SCHEMBL8980113 0.83 ALDH1A1 (0.42) ALDH1A1LMNAHSD17B10ALOX15MGAM
SCHEMBL17617122 0.83 ALDH1A1 (0.42) ALDH1A1LMNAHSD17B10ALOX15MGAM
SCHEMBL17617126 0.83 ALDH1A1 (0.42) ALDH1A1LMNAHSD17B10ALOX15MGAM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2693896-B1 FRUITY FLAVORED COCOA PRODUCTS AND PROCESSES FOR PRODUCING SUCH COCOA PRODUCTS OLAM INTERNATIONAL LTD (SG) 2018-09-12 EP claimed
US-9362595-B2 Nonaqueous electrolytic solution and energy storage device using same UBE INDUSTRIES, LTD. (JP) 2016-06-07 US claimed
US-20140030609-A1 NONAQUEOUS ELECTROLYTIC SOLUTION AND ENERGY STORAGE DEVICE USING SAME UBE INDUSTRIES, LTD. (JP) 2014-01-30 US claimed
CN-1177645-C DMC complex catalyst and process for preparing the same ���ʿ����о����޹�˾ 2004-12-01 CN claimed
US-6699961-B2 DOUBLE METAL CYANIDE (DMC); SPECIFIC LIQUID IS ADDED AFTER FORMATION OF THE DMC CATALYST PARTICLES, WHICH EFFECTS A PHASE SEPARATION RESULTING IN AN AQUEOUS PHASE CONTAINING THE SALTS AND A CATALYST CONTAINING PHASE FLOATING THEREON SHELL OIL COMPANY 2004-03-02 US claimed
EP-1276562-B1 DMC COMPLEX CATALYST AND PROCESS FOR ITS PREPARATION SHELL INT RESEARCH (NL) 2003-09-17 EP claimed
CN-1426325-A DMC complex catalyst and process for its preparation SHELL INT RESEARCH (NL) 2003-06-25 CN claimed
US-20030069389-A1 Dmc complex catalyst and process for its preparation SHELL OIL COMPANY 2003-04-10 US claimed
EP-1276562-A1 DMC COMPLEX CATALYST AND PROCESS FOR ITS PREPARATION SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 2003-01-22 EP claimed
WO-2001072418-A1 DMC COMPLEX CATALYST AND PROCESS FOR ITS PREPARATION SHELL INTERNATIONALE RESEARCH MAATSCHAPPIJ B.V. (NL) 2001-10-04 WO claimed
CN-106602013-B Preparation method of sulfur-activated carbon/graphene composite material 中国科学院山西煤炭化学研究所 2020-11-27 CN disclosed
US-9586931-B2 Triazolyl derivatives as Syk inhibitors MERCK SHARP & DOHME CORP. (US) 2017-03-07 US disclosed
US-9362595-B2 Nonaqueous electrolytic solution and energy storage device using same UBE INDUSTRIES, LTD. (JP) 2016-06-07 US disclosed
US-20160083341-A1 METHOD FOR PRODUCING a-SUBSTITUTED CYSTEINE OR SALT THEREOF OR SYNTHETIC INTERMEDIATE OF a-SUBSTITUTED CYSTEINE API CORPORATION (JP) 2016-03-24 US disclosed
US-9173395-B2 Use of substituted isoquinolinones, isoquinolindiones, isoquinolintriones and dihydroisoquinolinones or in each case salts thereof as active agents against abiotic stress in plants BAYER INTELLECTUAL PROPERTY GMBH (DE) 2015-11-03 US disclosed
US-20030069389-A1 Dmc complex catalyst and process for its preparation SHELL OIL COMPANY 2003-04-10 US disclosed
WO-2003008482-A1 DOUBLE METAL COMPLEX CATALYST SHELL INTERNATIONALE RESEARCH MAATSCHAPPIJ B.V. (NL) 2003-01-30 WO disclosed
US-20030023022-A1 Double metal complex catalyst SHELL OIL COMPANY 2003-01-30 US disclosed
EP-1276562-A1 DMC COMPLEX CATALYST AND PROCESS FOR ITS PREPARATION SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 2003-01-22 EP disclosed
WO-2001072418-A1 DMC COMPLEX CATALYST AND PROCESS FOR ITS PREPARATION SHELL INTERNATIONALE RESEARCH MAATSCHAPPIJ B.V. (NL) 2001-10-04 WO 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-20160083341-A1 METHOD FOR PRODUCING a-SUBSTITUTED CYSTEINE OR SALT THEREOF OR SYNTHETIC INTERMEDIATE OF a-SUBSTITUTED CYSTEINE MGMT, GSTA1, CBS ALDH1A1 236/4885LMNA 4014/4885HSD17B10 437/4885
US-20030069389-A1 Dmc complex catalyst and process for its preparation INO80C, DKC1, MLEC ALDH1A1 4525/4885LMNA 80/4885HSD17B10 877/4885

“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.