SCHEMBL1106982

SCHEMBL1106982

CC(C)NC(=O)OC(C)C

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 4/20 0.46
HTT P42858 1/20 0.43
ALOX15 P16050 2/20 0.40
SMN1; SMN2 Q16637 2/20 0.39
HPGD P15428 2/20 0.39
RAB9A P51151 2/20 0.39
NPC1 O15118 1/20 0.39
CYP1A2 P05177 1/20 0.39
CYP2D6 P10635 1/20 0.39
CYP2C9 P11712 1/20 0.39
CYP2C19 P33261 1/20 0.39
CA12 O43570 1/20 0.39
CA1 P00915 1/20 0.39
CA2 P00918 1/20 0.39
MMP1 P03956 1/20 0.39
MMP2 P08253 1/20 0.39
MMP9 P14780 1/20 0.39
MMP8 P22894 1/20 0.39
CA9 Q16790 1/20 0.39
KDM4E B2RXH2 1/20 0.37

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
SCHEMBL19810547 0.97 TSHR (0.43) TSHRHTTALOX15SMN1; SMN2HPGD
Ammonia Solution, Strong SCHEMBL1930552 0.97 TSHR (0.43) TSHRHTTALOX15SMN1; SMN2HPGD
SCHEMBL31650247 0.84 TSHR (0.37) TSHRHTTALOX15SMN1; SMN2HPGD
SCHEMBL11744998 0.81 TSHR (0.43) TSHRHTTALOX15SMN1; SMN2HPGD
SCHEMBL11544318 0.81 TSHR (0.43) TSHRHTTALOX15SMN1; SMN2HPGD
SCHEMBL21676258 0.80 CTSK (0.38) TSHRHTTALOX15SMN1; SMN2HPGD
SCHEMBL25082885 0.79 TSHR (0.36) TSHRHTTRAB9ACA12CA1
SCHEMBL22372338 0.79 TSHR (0.41) TSHRHTTRAB9ACA12CA1
SCHEMBL13951043 0.79 TSHR (0.42) TSHRHTTALOX15SMN1; SMN2HPGD
SCHEMBL23126298 0.79 TSHR (0.42) TSHRHTTALOX15SMN1; SMN2HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109689704-A The method for preparing polymer composition 巴斯夫欧洲公司 2019-04-26 CN claimed
JP-4795589-B2 2011-10-19 JP claimed
EP-1272500-A2 PROCESS FOR PREPARING 6-O-ALKENYL-SUBSITUTED ERYTHROMYCIN DERIVATIVES Abbott Laboratories (US) 2003-01-08 EP claimed
WO-2000078773-A2 PROCESS FOR PREPARING 6-O-ALKENYL-SUBSTITUTED ERYTHROMYCIN DERIV ATIVES ABBOTT LABORATORIES (US) 2000-12-28 WO 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-12037405-B2 Anti-CD70 antibody drug conjugates AMBRX, INC. 2024-07-16 US disclosed
US-12037405-B2 Anti-CD70 antibody drug conjugates AMBRX, INC. 2024-07-16 US disclosed
US-20240218011-A1 GLUCOCORTICOID RECEPTOR AGONISTS AND CONJUGATES THEREOF FIREFLY BIO, INC. 2024-07-04 US disclosed
WO-2024049769-A2 PATTERNED RELEASE LAYERS, AND METHODS OF MAKING AND USING THEM IN DEVICE MANUFACTURING TERECIRCUITS CORPORATION (US) 2024-03-07 WO disclosed
US-20240066047-A1 ANTIBODY-DRUG CONJUGATES COMPRISING A CYCLIC DINUCLEOTIDE TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2024-02-29 US disclosed
US-20240067642-A1 COMPOUNDS AND USES THEREOF FOGHORN THERAPEUTICS INC. 2024-02-29 US disclosed
US-20240072809-A1 ASGPR-BINDING COMPOUNDS FOR THE DEGRADATION OF EXTRACELLULAR PROTEINS AVILAR THERAPEUTICS, INC. (US) 2024-02-29 US disclosed
EP-0492556-A1 Continuous process for the preparation of isocyanates ENICHEM SYNTHESIS S.p.A. (IT) 1992-07-01 EP disclosed
CN-1058508-A This new bacterial strain of mould (Drechslera) Pseudomonas of moral and contain the weed control agent of this bacterial strain and weeds control mix preparation MITSUI TOATSU CHEMICALS (JP) 1992-02-12 CN disclosed
EP-0311642-A4 TEMPERATURE ADAPTABLE TEXTILE FIBERS AND METHOD OF PREPARING SAME US COMMERCE (US) 1991-04-24 EP disclosed
US-4908238-A Temperature adaptable textile fibers and method of preparing same THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF AGRICULTURE (US) 1990-03-13 US disclosed
US-4851291-A Temperature adaptable textile fibers and method of preparing same THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF AGRICULTURE (US) 1989-07-25 US disclosed
EP-0311642-A1 TEMPERATURE ADAPTABLE TEXTILE FIBERS AND METHOD OF PREPARING SAME. US COMMERCE (US) 1989-04-19 EP disclosed
WO-1987007854-A1 TEMPERATURE ADAPTABLE TEXTILE FIBERS AND METHOD OF PREPARING SAME UNITED STATES OF AMERICA, REPRESENTED BY THE SECRE (US) 1987-12-30 WO disclosed
US-4028344-A FOAMING AGENTS, FREE RADICAL INITIATORS PENNWALT CORPORATION (US) 1977-06-07 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 (5 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-20240066047-A1 ANTIBODY-DRUG CONJUGATES COMPRISING A CYCLIC DINUCLEOTIDE STING1, TLR9, CGAS TSHR 2611/4885HTT 3938/4885ALOX15 2253/4885
US-12037405-B2 Anti-CD70 antibody drug conjugates CD74, CD63, CD47 TSHR 3236/4885HTT 2355/4885ALOX15 4277/4885
US-20240218011-A1 GLUCOCORTICOID RECEPTOR AGONISTS AND CONJUGATES THEREOF NR3C1, NR3C2, MC2R TSHR 179/4885HTT 3360/4885ALOX15 1205/4885
US-20240239828-A1 MANNOSE 6-PHOSPHATE OR ASGPR RECEPTOR BINDING COMPOUNDS FOR THE DEGRADATION OF EXTRACELLULAR PROTEINS M6PR, ASGR1, IGF2R TSHR 560/4885HTT 4400/4885ALOX15 2569/4885
US-20240067642-A1 COMPOUNDS AND USES THEREOF VHL, TFEB, BECN1 TSHR 4793/4885HTT 304/4885ALOX15 3136/4885

“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.