SCHEMBL203099

SCHEMBL203099

CC1(CCC(=O)O)OCCO1

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.39
SLC15A2 Q16348 1/20 0.39
EGLN1 Q9GZT9 2/20 0.35
ALKBH5 Q6P6C2 1/20 0.35
SUCNR1 Q9BXA5 1/20 0.35
FFAR3 O14843 1/20 0.35
HDAC3 O15379 1/20 0.35
HDAC1 Q13547 1/20 0.35
HDAC2 Q92769 1/20 0.35
HDAC8 Q9BY41 1/20 0.35
TSHR P16473 2/20 0.33
CYP26A1 O43174 1/20 0.33
CYP26B1 Q9NR63 1/20 0.33
KDM4E B2RXH2 1/20 0.33
KDM6B O15054 1/20 0.33
KDM5C P41229 1/20 0.33
PHF8 Q9UPP1 1/20 0.33
KDM2A Q9Y2K7 1/20 0.33
GLA P06280 1/20 0.32
SLC22A6 Q4U2R8 1/20 0.32

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
SCHEMBL11245204 0.87 LMNA (0.40) LMNASLC15A2TSHRSLC22A6ALDH1A1
SCHEMBL1705915 0.85 LMNA (0.44) LMNATSHRSLC22A6ALDH1A1AKR1B1
SCHEMBL3154691 0.84 ALDH1A1 (0.41) LMNASLC15A2ALDH1A1
SCHEMBL27882078 0.84 TSHR (0.46) LMNATSHRSLC22A6ALDH1A1AKR1B1
SCHEMBL5124190 0.84 TSHR (0.46) LMNATSHRSLC22A6ALDH1A1AKR1B1
SCHEMBL20708377 0.81 LMNA (0.39) LMNAKDM4EALDH1A1MAPK1
SCHEMBL11538765 0.80 SMN1; SMN2 (0.31) KDM4E
SCHEMBL3474604 0.80 TSHR (0.37) TSHRALDH1A1
SCHEMBL18402511 0.79 LMNA (0.33) LMNASLC15A2FFAR3HDAC3HDAC1
SCHEMBL26061824 0.78 EPHX1 (0.34) LMNASLC15A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113861014-A Levulinic acid-13C, preparation method and application 长沙贝塔医药科技有限公司 2021-12-31 CN claimed
CN-113861014-B Levulinic acid (ACA)13C, preparation method and application 长沙贝塔医药科技有限公司 2024-05-03 CN disclosed
CN-113861014-B Levulinic acid (ACA)13C, preparation method and application 长沙贝塔医药科技有限公司 2024-05-03 CN disclosed
CN-113861014-A Levulinic acid-13C, preparation method and application 长沙贝塔医药科技有限公司 2021-12-31 CN disclosed
CN-113861014-A Levulinic acid-13C, preparation method and application 长沙贝塔医药科技有限公司 2021-12-31 CN disclosed
US-8088788-B2 Substituted fused[1,2] imidazo[4,5-c] ring compounds and methods 3M INNOVATIVE PROPERTIES COMPANY (US) 2012-01-03 US disclosed
US-7968563-B2 Oxime and hydroxylamine substituted imidazo[4,5-c] ring compounds and methods 3M INNOVATIVE PROPERTIES COMPANY (US) 2011-06-28 US disclosed
US-7897767-B2 Oxime substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY (US) 2011-03-01 US disclosed
US-20100069427-A9 Oxime and Hydroxylamine Substituted Imidazo[4,5-c] Ring Compounds and Methods COLEY PHARMACEUTICAL GROUP, INC. (US) 2010-03-18 US disclosed
US-20100048654-A1 USE OF VALSARTAN OR ITS METABOLITE TO IN HIBIT PLATELET AGGREGATION NOVARTIS PHARMACEUTICALS CORPORATION 2010-02-25 US disclosed
WO-2007106852-A2 SUBSTITUTED FUSED[1,2]IMIDAZO[4,5-C] RING COMPOUNDS AND METHODS COLEY PHARMACEUTICAL GROUP, INC. (US) 2007-09-20 WO disclosed
WO-2006086634-A2 OXIME AND HYDROXYLAMINE SUBSTITUTED IMIDAZO[4,5-C] RING COMPOUNDS AND METHODS COLEY PHARMACEUTICAL GROUP, INC. (US) 2006-08-17 WO disclosed
EP-1685129-A2 OXIME SUBSTITUTED IMIDAZO RING COMPOUNDS 3M Innovative Properties Company (US) 2006-08-02 EP disclosed
EP-1505965-B1 USE OF THE METABOLITE OF VALSARTAN TO INHIBIT PLATELET AGGREGATION NOVARTIS AG (CH) 2006-08-02 EP disclosed
US-20050197372-A1 Use of valsartan or its metabolite to inhibit platelet aggregation MALININ ALEX (US) 2005-09-08 US disclosed
WO-2005048933-A2 OXIME SUBSTITUTED IMIDAZO RING COMPOUNDS 3M INNOVATIVE PROPERTIES COMPANY (US) 2005-06-02 WO disclosed
EP-1505965-A1 USE OF VALSARTAN OT ITS METABOLITE TO INHIBIT PLATELET AGGREGATION Novartis AG (CH) 2005-02-16 EP disclosed
WO-2003094915-A1 USE OF VALSARTAN OT ITS METABOLITE TO INHIBIT PLATELET AGGREGATION NOVARTIS AG (CH) 2003-11-20 WO disclosed
US-6197774-B1 THERAPY FOR ASTHMA, SKIN DISORDERS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2001-03-06 US disclosed
EP-0244948-A2 Triazolopyrimidine herbicides SCHERING AGROCHEMICALS LIMITED (GB) 1987-11-11 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 (3 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-20100069427-A9 Oxime and Hydroxylamine Substituted Imidazo[4,5-c] Ring Compounds and Methods IFNG, IL4, IRF3 LMNA 2435/4885SLC15A2 3885/4885EGLN1 285/4885
US-20100048654-A1 USE OF VALSARTAN OR ITS METABOLITE TO IN HIBIT PLATELET AGGREGATION PDGFRA, PLAT, PTAFR LMNA 3758/4885SLC15A2 2068/4885EGLN1 453/4885
US-20050197372-A1 Use of valsartan or its metabolite to inhibit platelet aggregation PTAFR, PDGFRA, ACE LMNA 3943/4885SLC15A2 2621/4885EGLN1 1586/4885

“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.