SCHEMBL1483249

SCHEMBL1483249

COC(=O)c1ccc(C(=O)O)cc1O

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA12 O43570 6/20 0.65
CA1 P00915 6/20 0.65
CA2 P00918 6/20 0.65
CA7 P43166 6/20 0.65
CA9 Q16790 6/20 0.65
CA14 Q9ULX7 6/20 0.65
PDK2 Q15119 1/20 0.65
PDK4 Q16654 1/20 0.65
GAA P10253 4/20 0.61
XDH P47989 2/20 0.56
SMN1; SMN2 Q16637 2/20 0.56
KDM4E B2RXH2 5/20 0.53
MAPT P10636 3/20 0.53
POLB P06746 2/20 0.53
L3MBTL1 Q9Y468 2/20 0.53
CA4 P22748 2/20 0.53
CA6 P23280 2/20 0.53
PTGS2 P35354 2/20 0.53
LMNA P02545 3/20 0.53
TSHR P16473 1/20 0.53

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
SCHEMBL162631 0.89 CA12 (0.71) CA12CA1CA2CA7CA9
SCHEMBL29501115 0.89 CA12 (0.71) CA12CA1CA2CA7CA9
SCHEMBL10564137 0.87 CA12 (0.69) CA12CA1CA2CA7CA9
SCHEMBL1647438 0.85 CA12 (0.65) CA12CA1CA2CA7CA9
SCHEMBL9122345 0.85 CA12 (0.67) CA12CA1CA2CA7CA9
SCHEMBL5082071 0.85 SMN1; SMN2 (0.65) CA12CA1CA2CA7CA9
SCHEMBL820141 0.85 KDM4E (0.55) CA12CA1CA2CA7CA9
SCHEMBL29699657 0.85 KDM4E (0.55) CA12CA1CA2CA7CA9
SCHEMBL20414588 0.84 CA12 (0.62) CA12CA1CA2CA7CA9
SCHEMBL1018113 0.83 KDM4E (0.53) CA12CA1CA2CA7CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112980041-A Preparation method of anti-yellowing high-strength expanded polystyrene heat-insulating material 长沙三思新材料科技有限公司 2021-06-18 CN claimed
CN-118079661-A Two-dimensional porous frame-based mixed matrix membrane, and preparation method and separation application thereof 中国科学院大连化学物理研究所 2024-05-28 CN disclosed
US-20230160000-A1 SYNTHESIS OF NOVEL DISULFIDE LINKER BASED NUCLEOTIDES AS REVERSIBLE TERMINATORS FOR DNA SEQUENCING BY SYNTHESIS THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2023-05-25 US disclosed
US-20230160000-A1 SYNTHESIS OF NOVEL DISULFIDE LINKER BASED NUCLEOTIDES AS REVERSIBLE TERMINATORS FOR DNA SEQUENCING BY SYNTHESIS THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2023-05-25 US disclosed
US-20230028321-A1 NUCLEOTIDE DERIVATIVES AND METHODS OF USE THEREOF THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2023-01-26 US disclosed
US-20230028388-A1 DESIGN AND SYNTHESIS OF NOVEL DISULFIDE LINKER BASED NUCLEOTIDES AS REVERSIBLE TERMINATORS FOR DNA SEQUENCING BY SYNTHESIS THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2023-01-26 US disclosed
US-20220411860-A1 DESIGN AND SYNTHESIS OF NOVEL DISULFIDE LINKER BASED NUCLEOTIDES AS REVERSIBLE TERMINATORS FOR DNA SEQUENCING BY SYNTHESIS THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2022-12-29 US disclosed
CN-114728064-A Antibody-containing preparation 中外制药株式会社 2022-07-08 CN disclosed
WO-2021252723-A1 LINKER-FUNCTIONALIZED METAL-ORGANIC FRAMEWORK FOR POLYSULFIDE TETHERING IN LITHIUM-SULFUR BATTERIES THE JOHNS HOPKINS UNIVERSITY (US) 2021-12-16 WO disclosed
US-11085076-B2 Synthesis of novel disulfide linker based nucleotides as reversible terminators for DNA sequencing by synthesis THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2021-08-10 US disclosed
US-20080027068-A1 HETEROCYCLIC COMPOUNDS AND THROMBOPOIETIN RECEPTOR ACTIVATORS NISSAN CHEMICAL INDUSTRIES LIMITED (JP) 2008-01-31 US disclosed
EP-1879940-A1 PREPARATION OF LOW-ACID POLYALKYLENE TEREPHTHALATE AND PREPARATION OF MACROCYCLIC POLYESTER OLIGOMER THEREFROM Cyclics Corporation (US) 2008-01-23 EP disclosed
US-20060235233-A1 Methods for removing catalyst residue from a depolymerization process stream CYCLICS CORPORATION (US) 2006-10-19 US disclosed
US-20060235186-A1 Use of a residual oligomer recyclate in the production of macrocyclic polyester oligomer CYCLICS CORPORATION (US) 2006-10-19 US disclosed
US-20060235185-A1 Preparation of low-acid polyalkylene terephthalate and preparation of macrocyclic polyester oligomer therefrom CYCLICS CORPORATION (US) 2006-10-19 US disclosed
WO-2006104821-A1 PREPARATION OF LOW-ACID POLYALKYLENE TEREPHTHALATE AND PREPARATION OF MACROCYCLIC POLYESTER OLIGOMER THEREFROM CYCLICS CORPORAITON (US) 2006-10-05 WO disclosed
CN-1798739-A 3-alkylidenehydrazino substituted heteroaryl compounds as thrombopoietin receptor activators NISSAN CHEMICAL IND LTD (JP) 2006-07-05 CN disclosed
US-20060094694-A1 Heterocyclic compounds and thrombopoietin receptor activators NISSAN CHEMICAL INDUSTRIES LIMITED (JP) 2006-05-04 US disclosed
EP-1636192-A1 3-ALKYLIDENEHYDRAZINO SUBSTITUTED HETEROARYL COMPOUNDS AS THROMBOPOIETIN RECEPTOR ACTIVATORS Nissan Chemical Industries, Ltd. (JP) 2006-03-22 EP disclosed
WO-2004108683-A1 3-ALKYLIDENEHYDRAZINO SUBSTITUTED HETEROARYL COMPOUNDS AS THROMBOPOIETIN RECEPTOR ACTIVATORS NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2004-12-16 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 (8 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-20220411860-A1 DESIGN AND SYNTHESIS OF NOVEL DISULFIDE LINKER BASED NUCLEOTIDES AS REVERSIBLE TERMINATORS FOR DNA SEQUENCING BY SYNTHESIS POLL, POLQ, POLB CA12 4147/4885CA1 3823/4885CA2 4528/4885
US-20060094694-A1 Heterocyclic compounds and thrombopoietin receptor activators NR2C2, ROR1, NR0B2 CA12 1026/4885CA1 2516/4885CA2 2631/4885
US-20230028388-A1 DESIGN AND SYNTHESIS OF NOVEL DISULFIDE LINKER BASED NUCLEOTIDES AS REVERSIBLE TERMINATORS FOR DNA SEQUENCING BY SYNTHESIS RNGTT, POLRMT, MTR CA12 4243/4885CA1 3884/4885CA2 4348/4885
US-20060235233-A1 Methods for removing catalyst residue from a depolymerization process stream MPO, CAT, LPO CA12 526/4885CA1 386/4885CA2 1245/4885
US-20080027068-A1 HETEROCYCLIC COMPOUNDS AND THROMBOPOIETIN RECEPTOR ACTIVATORS NR2C2, ROR1, NR0B2 CA12 1203/4885CA1 2676/4885CA2 2832/4885
US-11085076-B2 Synthesis of novel disulfide linker based nucleotides as reversible terminators for DNA sequencing by synthesis POLRMT, RNGTT, MTR CA12 4130/4885CA1 3850/4885CA2 4253/4885
US-20230028321-A1 NUCLEOTIDE DERIVATIVES AND METHODS OF USE THEREOF POLRMT, NSUN2, NUDT1 CA12 3711/4885CA1 4662/4885CA2 4663/4885
US-20230160000-A1 SYNTHESIS OF NOVEL DISULFIDE LINKER BASED NUCLEOTIDES AS REVERSIBLE TERMINATORS FOR DNA SEQUENCING BY SYNTHESIS POLRMT, RNGTT, MTR CA12 4130/4885CA1 3850/4885CA2 4253/4885

“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.