SCHEMBL1138474

SCHEMBL1138474

CC(=O)NC1CC(C)(C)N(OC(C)=O)C(C)(C)C1

nearest known ligand 0.46

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.46
SMN1; SMN2 Q16637 1/20 0.40
KMT2A Q03164 3/20 0.39
ALDH1A1 P00352 4/20 0.38
ESR1 P03372 1/20 0.38
HSD17B10 Q99714 1/20 0.38
ATM Q13315 1/20 0.34
KDM4E B2RXH2 4/20 0.34
GAA P10253 3/20 0.34
ALOX15 P16050 1/20 0.32
MEN1 O00255 1/20 0.32
CA1 P00915 2/20 0.30
CA2 P00918 2/20 0.30
CA12 O43570 1/20 0.30
CA9 Q16790 1/20 0.30
EPHX2 P34913 1/20 0.30
TACR1 P25103 1/20 0.30
TACR3 P29371 1/20 0.30

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
SCHEMBL25697941 0.85 TSHR (0.43) TSHRSMN1; SMN2KMT2AALDH1A1ESR1
SCHEMBL18217967 0.84 SMN1; SMN2 (0.36) TSHRSMN1; SMN2KMT2AALDH1A1ATM
SCHEMBL1139079 0.83 SMN1; SMN2 (0.40) TSHRSMN1; SMN2KMT2AALDH1A1ESR1
SCHEMBL12921994 0.80 TSHR (0.61) TSHRSMN1; SMN2KMT2AALDH1A1ESR1
SCHEMBL4982955 0.79 ALDH1A1 (0.36) TSHRSMN1; SMN2KMT2AALDH1A1ATM
Phosphoric Acid SCHEMBL3801977 0.78 KDM4E (0.35) TSHRSMN1; SMN2KMT2AALDH1A1ATM
Phosphoric Acid SCHEMBL3801972 0.78 KDM4E (0.35) TSHRSMN1; SMN2KMT2AALDH1A1ATM
SCHEMBL16341866 0.78 TSHR (0.48) TSHRKMT2AALDH1A1ESR1HSD17B10
SCHEMBL2857927 0.78 SMN1; SMN2 (0.37) TSHRSMN1; SMN2KMT2AGAAMEN1
SCHEMBL8613134 0.77 HDAC4 (0.39) TSHRKMT2AALDH1A1ATMKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9732168-B2 Method of preparing ethylene polymers by controlled high pressure polymerization BASF SE (DE) 2017-08-15 US disclosed
US-9732168-B2 Method of preparing ethylene polymers by controlled high pressure polymerization BASF SE (DE) 2017-08-15 US disclosed
US-20130150542-A1 Method Of Preparing Ethylene Polymers By Controlled High Pressure Polymerization BASF SE (DE) 2013-06-13 US disclosed
US-20130150542-A1 Method Of Preparing Ethylene Polymers By Controlled High Pressure Polymerization BASF SE (DE) 2013-06-13 US disclosed
US-8168725-B2 Degradation of polypropylene with hydroxylamine ester compositions BASF SE (DE) 2012-05-01 US disclosed
US-8168725-B2 Degradation of polypropylene with hydroxylamine ester compositions BASF SE (DE) 2012-05-01 US disclosed
US-20110207892-A1 DEGRADATION OF POLYPROPYLENE WITH HYDROXYLAMINE ESTER COMPOSITIONS ROTH MICHAEL 2011-08-25 US disclosed
US-20110207892-A1 DEGRADATION OF POLYPROPYLENE WITH HYDROXYLAMINE ESTER COMPOSITIONS ROTH MICHAEL 2011-08-25 US disclosed
US-7956109-B2 Degradation of polypropylene with hydroxylamine ester compositions BASF SE (DE) 2011-06-07 US disclosed
US-7956109-B2 Degradation of polypropylene with hydroxylamine ester compositions BASF SE (DE) 2011-06-07 US disclosed
EP-1404729-B1 METHOD OF GRAFTING ETHYLENICALLY UNSATURATED CARBOXYLIC ACID DERIVATIVES ONTO THERMOPLASTIC POLYMERS USING HYDROXYLAMINE ESTERS CIBA SC HOLDING AG (CH) 2007-11-21 EP disclosed
US-7230042-B2 Flame retardant polymer compositions containing hydroxylamine esters CIBA SPECIALTY CHEMICALS CORP. (US) 2007-06-12 US disclosed
US-7230042-B2 Flame retardant polymer compositions containing hydroxylamine esters CIBA SPECIALTY CHEMICALS CORP. (US) 2007-06-12 US disclosed
US-20060128903-A1 Process for the controlled increase in the molecular weight of polyethylenes ROTH MICHAEL 2006-06-15 US disclosed
EP-1282630-B1 Process for Reducing the Molecular Weight of Polypropylene Using Hydroxylamine Esters CIBA SC HOLDING AG (CH) 2006-05-10 EP disclosed
EP-1655303-A2 Hydroxylamine esters as polimerization initiators Ciba SC Holding AG (CH) 2006-05-10 EP disclosed
US-7030196-B2 Process for reducing the molecular weight of polypropylene CIBA SPECIALTY CHEMICALS CORPORATION (US) 2006-04-18 US disclosed
US-20030216494-A1 Hydroxylamine esters as polymerization initiators CIBA SPECIALTY CHEMICALS CORP. 2003-11-20 US disclosed
EP-1282630-A1 HYDROXYLAMINE ESTERS AS POLYMERIZATION INITIATORS Ciba SC Holding AG (CH) 2003-02-12 EP disclosed
WO-2001090113-A1 HYDROXYLAMINE ESTERS AS POLYMERIZATION INITIATORS CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2001-11-29 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 (1 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-20030216494-A1 Hydroxylamine esters as polymerization initiators PNMT, HPGDS, HAAO TSHR 2473/4885SMN1; SMN2 4814/4885KMT2A 1030/4885

“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.