SCHEMBL6347286

SCHEMBL6347286

CC(C)(C)OC(=O)NCc1ccc(Cl)cc1

nearest known ligand 0.72

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
GAA P10253 1/20 0.72
MEN1 O00255 4/20 0.58
KMT2A Q03164 4/20 0.58
CYP2C19 P33261 2/20 0.55
CYP1A2 P05177 1/20 0.55
L3MBTL1 Q9Y468 1/20 0.54
CYP2C9 P11712 1/20 0.54
NAMPT P43490 2/20 0.52
SMN1; SMN2 Q16637 2/20 0.51
HTT P42858 1/20 0.51
NPSR1 Q6W5P4 1/20 0.51
ALDH1A1 P00352 2/20 0.50
LMNA P02545 1/20 0.50
HPGD P15428 1/20 0.50
NPC1 O15118 1/20 0.50
RAB9A P51151 1/20 0.50
CA1 P00915 1/20 0.49
CA2 P00918 1/20 0.49
DRD2 P14416 1/20 0.49

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
SCHEMBL3180689 0.91 L3MBTL1 (0.61) GAAL3MBTL1NAMPTNPSR1CA1
SCHEMBL16192930 0.90 GAA (0.61) GAAMEN1KMT2ACYP2C19CYP1A2
SCHEMBL12133145 0.89 GAA (0.60) GAAMEN1KMT2ACYP2C19CYP1A2
SCHEMBL3284231 0.87 GAA (0.56) GAAL3MBTL1NAMPTNPSR1CA1
SCHEMBL1724201 0.86 GAA (0.60) GAAMEN1KMT2ACYP2C19CYP1A2
SCHEMBL24011136 0.85 GAA (0.58) GAAMEN1KMT2ASMN1; SMN2LMNA
SCHEMBL5796279 0.85 L3MBTL1 (0.56) GAAMEN1KMT2ACYP2C19L3MBTL1
SCHEMBL15259134 0.85 L3MBTL1 (0.56) GAAKMT2AL3MBTL1NAMPTNPSR1
SCHEMBL1164796 0.85 L3MBTL1 (0.56) GAAL3MBTL1NAMPTNPSR1CA1
SCHEMBL12685839 0.85 L3MBTL1 (0.56) GAAL3MBTL1NAMPTNPSR1CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106674080-A Synthesis method of panobinostat 南京卡文迪许生物工程技术有限公司 2017-05-17 CN claimed
US-20250092027-A1 ISOINDOLINONE INHIBITORS OF THE MDM2-P53 INTERACTION HAVING ANTICANCER ACTIVITY ASTEX THERAPEUTICS LIMITED (GB) 2025-03-20 US disclosed
CN-115572252-B Isoindolinone inhibitors of MDM2-P53 interaction with anticancer activity 阿斯泰克斯治疗有限公司 2025-02-25 CN disclosed
US-12071429-B2 Isoindolinone inhibitors of the MDM2-P53 interaction having anticancer activity ASTEX THERAPEUTICS LIMITED (GB) 2024-08-27 US disclosed
EP-4151633-A1 INTERMEDIATES OF ISOINDOLINONE INHIBITORS OF THE MDM2-P53 INTERACTION HAVING ANTICANCER ACTIVITY Astex Therapeutics Limited (GB) 2023-03-22 EP disclosed
CN-115572252-A Isoindolinone inhibitors of MDM2-P53 interaction with anti-cancer activity 阿斯泰克斯治疗有限公司 2023-01-06 CN disclosed
EP-3356350-B1 ISOINDOLINONE INHIBITORS OF THE MDM2-P53 INTERACTION HAVING ANTICANCER ACTIVITY ASTEX THERAPEUTICS LTD (GB) 2022-11-16 EP disclosed
CN-108290871-B Isoindolinone inhibitors of MDM2-P53 interaction with anti-cancer activity 阿斯泰克斯治疗有限公司 2022-08-23 CN disclosed
US-20210276984-A1 ISOINDOLINONE INHIBITORS OF THE MDM2-P53 INTERACTION HAVING ANTICANCER ACTIVITY ASTEX THERAPEUTICS LIMITED (GB) 2021-09-09 US disclosed
US-20210276984-A1 ISOINDOLINONE INHIBITORS OF THE MDM2-P53 INTERACTION HAVING ANTICANCER ACTIVITY ASTEX THERAPEUTICS LIMITED (GB) 2021-09-09 US disclosed
US-20190016708-A1 ISOINDOLINONE INHIBITORS OF THE MDM2-P53 INTERACTION HAVING ANTICANCER ACTIVITY ASTEX THERAPEUTICS LIMITED (GB) 2019-01-17 US disclosed
WO-2019006422-A1 CORE-TO-SURFACE POLYMERIZATION FOR THE SYNTHESIS OF STAR POLYMERS AND USES THEREOF MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2019-01-03 WO disclosed
EP-3356350-A1 ISOINDOLINONE INHIBITORS OF THE MDM2-P53 INTERACTION HAVING ANTICANCER ACTIVITY Astex Therapeutics Limited (GB) 2018-08-08 EP disclosed
CN-108368101-A SELECTIVE NR2B ANTAGONISTS 百时美施贵宝公司 2018-08-03 CN disclosed
US-20080269196-A1 6-Arylalkylamino-2,3,4,5-Tetrahydro-1H-Benzo[D]Azepines as 5-Ht2c Receptor Agonists ELI LILLY AND COMPANY 2008-10-30 US disclosed
US-20080269196-A1 6-Arylalkylamino-2,3,4,5-Tetrahydro-1H-Benzo[D]Azepines as 5-Ht2c Receptor Agonists ELI LILLY AND COMPANY 2008-10-30 US disclosed
US-6878736-B1 Histamine H3 receptor ligands JAMES BLACK FOUNDATION LIMITED (GB) 2005-04-12 US disclosed
EP-1056733-B1 HISTAMINE H3 RECEPTOR LIGANDS BLACK JAMES FOUNDATION (GB) 2004-01-07 EP disclosed
EP-1056733-A1 HISTAMINE H3 RECEPTOR LIGANDS JAMES BLACK FOUNDATION LIMITED (GB) 2000-12-06 EP disclosed
WO-1999042458-A1 HISTAMINE H3 RECEPTOR LIGANDS JAMES BLACK FOUNDATION LIMITED (GB) 1999-08-26 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 (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-12071429-B2 Isoindolinone inhibitors of the MDM2-P53 interaction having anticancer activity TP53, MDM2, TP53BP1 GAA 2315/4885MEN1 1609/4885KMT2A 3047/4885
US-20250092027-A1 ISOINDOLINONE INHIBITORS OF THE MDM2-P53 INTERACTION HAVING ANTICANCER ACTIVITY TP53, MDM2, TP53BP1 GAA 2342/4885MEN1 1624/4885KMT2A 3084/4885
US-20190016708-A1 ISOINDOLINONE INHIBITORS OF THE MDM2-P53 INTERACTION HAVING ANTICANCER ACTIVITY TP53, MDM2, TP53BP1 GAA 2315/4885MEN1 1609/4885KMT2A 3047/4885
US-20080269196-A1 6-Arylalkylamino-2,3,4,5-Tetrahydro-1H-Benzo[D]Azepines as 5-Ht2c Receptor Agonists HTR2C, HTR1A, HTR2A GAA 4045/4885MEN1 4387/4885KMT2A 1221/4885
US-20210276984-A1 ISOINDOLINONE INHIBITORS OF THE MDM2-P53 INTERACTION HAVING ANTICANCER ACTIVITY TP53, MDM2, TP53BP1 GAA 2315/4885MEN1 1609/4885KMT2A 3047/4885

“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.