SCHEMBL540695

SCHEMBL540695

CCC[C@@H](O)c1ccccc1

nearest known ligand 0.67

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.67
RIPK1 Q13546 1/20 0.61
AOC3 Q16853 7/20 0.55
KDM4E B2RXH2 2/20 0.52
L3MBTL1 Q9Y468 1/20 0.52
ALDH1A1 P00352 1/20 0.50
ASAH1 Q13510 1/20 0.45
TSHR P16473 1/20 0.44
GAA P10253 1/20 0.44
PPARG P37231 1/20 0.44
PPARA Q07869 1/20 0.44

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
SCHEMBL1295513 1.00 LMNA (0.67) LMNARIPK1AOC3KDM4EL3MBTL1
SCHEMBL348229 1.00 LMNA (0.67) LMNARIPK1AOC3KDM4EL3MBTL1
SCHEMBL28617318 1.00 LMNA (0.67) LMNARIPK1AOC3KDM4EL3MBTL1
Phenylpropanol SCHEMBL9863274 0.94 LMNA (0.79) LMNARIPK1AOC3KDM4EL3MBTL1
Acetic Acid SCHEMBL29265549 0.92 LMNA (0.57) LMNARIPK1AOC3KDM4EL3MBTL1
Acetic Acid SCHEMBL29265550 0.92 LMNA (0.57) LMNARIPK1AOC3KDM4EL3MBTL1
Fenipentol SCHEMBL11351770 0.88 LMNA (0.64) LMNARIPK1AOC3KDM4EL3MBTL1
Fenipentol SCHEMBL21837 0.88 LMNA (0.64) LMNARIPK1AOC3KDM4EL3MBTL1
Fenipentol SCHEMBL11573151 0.88 LMNA (0.64) LMNARIPK1AOC3KDM4EL3MBTL1
SCHEMBL21633858 0.87 LMNA (0.48) LMNARIPK1AOC3KDM4EALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10272072-B2 Compounds and compositions for the inhibition of NAMPT FORMA TM, LLC (US) 2019-04-30 US claimed
US-20170368039-A1 NOVEL COMPOUNDS AND COMPOSITIONS FOR THE INHIBITION OF NAMPT FORMA TM, LLC (US) 2017-12-28 US claimed
US-20140294805-A1 NOVEL COMPOUNDS AND COMPOSITIONS FOR THE INHIBITION OF NAMPT VALO EARLY DISCOVERY, INC. 2014-10-02 US claimed
US-12336981-B2 Compounds and compositions for the inhibition of NAMPT VALO HEALTH, INC. (US) 2025-06-24 US disclosed
WO-2024190722-A1 METHOD FOR IDENTIFYING OPTICAL ISOMER OF LOW-MOLECULAR-WEIGHT COMPOUND 国立大学法人大阪大学 2024-09-19 WO disclosed
CN-115745764-B Preparation method of milbelin intermediate 重庆华森制药股份有限公司 2024-03-12 CN disclosed
US-20230346753-A1 NOVEL COMPOUNDS AND COMPOSITIONS FOR THE INHIBITION OF NAMPT VALO HEALTH, INC. 2023-11-02 US disclosed
US-20230194486-A1 QUANTITATIVE CHIRALITY AND CONCENTRATION SENSING OF CHIRAL ANALYTES USING A RELAY ASSAY NATIONAL SCIENCE FOUNDATION 2023-06-22 US disclosed
CN-115745764-A Preparation method of milobalin intermediate 重庆华森制药股份有限公司 2023-03-07 CN disclosed
US-11547701-B2 Compounds and compositions for the inhibition of NAMPT VALO HEALTH, INC. (US) 2023-01-10 US disclosed
WO-2021225688-A1 QUANTITATIVE CHIRALITY AND CONCENTRATION SENSING OF CHIRAL ANALYTES USING A RELAY ASSAY GEORGETOWN UNIVERSITY (US) 2021-11-11 WO disclosed
WO-2000064911-A1 LIGANDS FOR METABOTROPIC GLUTAMATE RECEPTORS GEORGETOWN UNIVERSITY (US) 2000-11-02 WO disclosed
EP-0603278-A1 INDOLE DERIVATIVES AS 5-ALPHA-REDUCTASE INHIBITOR FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1994-06-29 EP disclosed
WO-1993005019-A1 INDOLE DERIVATIVES AS 5-ALPHA-REDUCTASE INHIBITOR FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1993-03-18 WO disclosed
US-4983739-A Optically active styrene compounds CIBA-GEIGY CORPORATION (US) 1991-01-08 US disclosed
US-4954592-A Optically active styrene derivatives, polymers obtained from these, complexes with iridium(I) and their use CIBA-GEIGY CORPORATION (US) 1990-09-04 US disclosed
US-4904790-A Optically active styrene compounds substituted by a pyridinyl group CIBA-GEIGY CORPORATION (US) 1990-02-27 US disclosed
US-4891412-A Optically active styrene derivatives, polymers obtained from these, complexes with iridium(I) and their use CIBA-GEIGY CORPORATION (US) 1990-01-02 US disclosed
US-4800224-A Optically active styrene derivatives, polymers obtained from these, complexes with iridium(I) and their use CIBA-GEIGY CORPORATION (US) 1989-01-24 US disclosed
EP-0251994-A1 Optically active styrene derivatives, polymers therefrom, complexes with iridium (I) and their use CIBA-GEIGY AG (CH) 1988-01-07 EP 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 (6 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-12336981-B2 Compounds and compositions for the inhibition of NAMPT NAMPT, NNMT, NNT LMNA 860/4885RIPK1 1927/4885AOC3 2433/4885
US-20170368039-A1 NOVEL COMPOUNDS AND COMPOSITIONS FOR THE INHIBITION OF NAMPT NAMPT, NNMT, NQO1 LMNA 1579/4885RIPK1 1529/4885AOC3 2579/4885
US-11547701-B2 Compounds and compositions for the inhibition of NAMPT NAMPT, NNMT, NQO1 LMNA 923/4885RIPK1 1817/4885AOC3 2447/4885
US-20140294805-A1 NOVEL COMPOUNDS AND COMPOSITIONS FOR THE INHIBITION OF NAMPT NAMPT, NNMT, NQO1 LMNA 1579/4885RIPK1 1529/4885AOC3 2579/4885
US-10272072-B2 Compounds and compositions for the inhibition of NAMPT NAMPT, NNMT, NQO1 LMNA 923/4885RIPK1 1817/4885AOC3 2447/4885
US-20230346753-A1 NOVEL COMPOUNDS AND COMPOSITIONS FOR THE INHIBITION OF NAMPT NAMPT, NNMT, NQO1 LMNA 1579/4885RIPK1 1529/4885AOC3 2579/4885

“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.