SCHEMBL7741371

SCHEMBL7741371

CC(C)OCCC(=O)OC(C)C

nearest known ligand 0.52

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.52
ALDH1A1 P00352 4/20 0.40
TSHR P16473 2/20 0.40
MAPT P10636 3/20 0.39
HTT P42858 1/20 0.36
HSD17B10 Q99714 2/20 0.36
ALOX15 P16050 1/20 0.36
CASP1 P29466 1/20 0.36
CASP7 P55210 1/20 0.36
CYP2D6 P10635 1/20 0.34
NOTUM Q6P988 1/20 0.34
GAA P10253 1/20 0.33
EPHX2 P34913 1/20 0.33
KDM4E B2RXH2 1/20 0.33
HPGD P15428 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
Cyclopropane SCHEMBL27363746 0.94 LMNA (0.47) LMNAALDH1A1TSHRMAPTHTT
SCHEMBL26199851 0.87 LMNA (0.46) LMNAALDH1A1TSHRMAPTHTT
SCHEMBL72471 0.82 LMNA (0.62) LMNAALDH1A1TSHRMAPTHTT
SCHEMBL13502946 0.81 ALDH1A1 (0.40) LMNAALDH1A1TSHREPHX2
SCHEMBL6651373 0.81 TSHR (0.55) LMNAALDH1A1TSHRMAPTHTT
SCHEMBL498581 0.81 LMNA (0.52) LMNAALDH1A1TSHRMAPTHTT
SCHEMBL17908830 0.80 LMNA (0.52) LMNAALDH1A1TSHRMAPTHTT
SCHEMBL17909443 0.80 LMNA (0.52) LMNAALDH1A1TSHRMAPTHTT
SCHEMBL31402602 0.79 LMNA (0.60) LMNAALDH1A1TSHRMAPTHTT
SCHEMBL3897660 0.79 LMNA (0.50) LMNAALDH1A1TSHRMAPTHTT

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
CN-109796339-A A kind of preparation method of 3- (2- ethylpropoxy) propionic acid -2- ethylpropyl 韶关市合众化工有限公司 2019-05-24 CN claimed
CN-109651147-A A kind of preparation method of 3- isopropoxy isopropyl propionate 韶关市合众化工有限公司 2019-04-19 CN claimed
US-6415614-B1 CONTROLLING VAPOR PRESSURE OF MIXTURE VISTEON GLOBAL TECHNOLOGIES, INC. 2002-07-09 US claimed
US-20240239828-A1 MANNOSE 6-PHOSPHATE OR ASGPR RECEPTOR BINDING COMPOUNDS FOR THE DEGRADATION OF EXTRACELLULAR PROTEINS AVILAR THERAPEUTICS, INC. (US) 2024-07-18 US disclosed
US-20240072809-A1 ASGPR-BINDING COMPOUNDS FOR THE DEGRADATION OF EXTRACELLULAR PROTEINS AVILAR THERAPEUTICS, INC. (US) 2024-02-29 US disclosed
US-11819551-B2 ASGPR-binding compounds for the degradation of extracellular proteins AVILAR THERAPEUTICS, INC. (US) 2023-11-21 US disclosed
US-20230233689-A1 Bifunctional Small Molecules to Target the Selective Degradation of Circulating Proteins UNIV YALE (US) 2023-07-27 US disclosed
CN-109651147-A A kind of preparation method of 3- isopropoxy isopropyl propionate 韶关市合众化工有限公司 2019-04-19 CN disclosed
CN-109651147-A A kind of preparation method of 3- isopropoxy isopropyl propionate 韶关市合众化工有限公司 2019-04-19 CN disclosed
CN-109651147-A A kind of preparation method of 3- isopropoxy isopropyl propionate 韶关市合众化工有限公司 2019-04-19 CN disclosed
CN-104203905-A Process for producing beta-alkoxypropionamide IDEMITSU KOSAN CO 2014-12-10 CN disclosed
US-20140193510-A1 Polymer-Agent Conjugates, Particles, Compositions, and Related Methods of Use CERULEAN PHARMA INC. (US) 2014-07-10 US disclosed
US-4978754-A REACTING B-ALKOXY-SUBSTITUTED CARBOXYLATE WITH CYCLIC AMINE, REMOVING ALCOHOL IN PRESENCE OF BASIC CATALYST MITSUI TOATSU CHEMICALS, INCORPORATED (JP) 1990-12-18 US disclosed
EP-0321256-A2 Process of preparing unsaturated carboxylic acid amides MITSUI TOATSU CHEMICALS, Inc. (JP) 1989-06-21 EP disclosed
US-4835175-A Indole derivatives pharmaceutical preparations based thereon, and β-receptor stimulation therewith SCHERING AKTIENGESELLSCHAFT (DE) 1989-05-30 US disclosed
US-3987089-A PLATINUM GROUP METAL SALT CATALYST, REOXIDIZING AGENT ROHM AND HAAS COMPANY (US) 1976-10-19 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 (4 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-11819551-B2 ASGPR-binding compounds for the degradation of extracellular proteins ASGR1, ENGASE, FCGR2A LMNA 2955/4885ALDH1A1 3319/4885TSHR 645/4885
US-20230233689-A1 Bifunctional Small Molecules to Target the Selective Degradation of Circulating Proteins ASGR1, LDLR, FCGR2A LMNA 3307/4885ALDH1A1 3256/4885TSHR 665/4885
US-20240239828-A1 MANNOSE 6-PHOSPHATE OR ASGPR RECEPTOR BINDING COMPOUNDS FOR THE DEGRADATION OF EXTRACELLULAR PROTEINS M6PR, ASGR1, IGF2R LMNA 2973/4885ALDH1A1 4019/4885TSHR 560/4885
US-20140193510-A1 Polymer-Agent Conjugates, Particles, Compositions, and Related Methods of Use LPXN, POLI, BRCA1 LMNA 461/4885ALDH1A1 1992/4885TSHR 3588/4885

“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.