SCHEMBL7123624

SCHEMBL7123624

CC(C)(C)OC(=O)N1CC(=O)C[C@H]1CO[Si](C)(C)C(C)(C)C

nearest known ligand 0.37

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.37
MEN1 O00255 2/20 0.34
KMT2A Q03164 2/20 0.34
TSHR P16473 2/20 0.34
L3MBTL1 Q9Y468 1/20 0.34
ATM Q13315 2/20 0.33
PARP1 P09874 1/20 0.33
FKBP1A P62942 1/20 0.33
TOP2A P11388 1/20 0.33
FAAH O00519 1/20 0.33
PDE8B O95263 1/20 0.32
LMNA P02545 1/20 0.31
USP2 O75604 1/20 0.31
SMN1; SMN2 Q16637 1/20 0.31

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
SCHEMBL31080875 1.00 ALDH1A1 (0.37) ALDH1A1MEN1KMT2ATSHRL3MBTL1
SCHEMBL585208 0.87 PARP1 (0.39) ALDH1A1MEN1KMT2ATSHRL3MBTL1
SCHEMBL585011 0.87 PARP1 (0.39) ALDH1A1MEN1KMT2ATSHRL3MBTL1
SCHEMBL27190406 0.86 TOP2A (0.34) FKBP1ATOP2A
SCHEMBL2842945 0.86 ALDH1A1 (0.36) ALDH1A1MEN1KMT2ATSHRL3MBTL1
SCHEMBL2842338 0.86 ALDH1A1 (0.36) ALDH1A1MEN1KMT2ATSHRL3MBTL1
SCHEMBL2838596 0.86 ALDH1A1 (0.36) ALDH1A1MEN1KMT2ATSHRL3MBTL1
SCHEMBL17930909 0.84 ALDH1A1 (0.34) ALDH1A1MEN1KMT2AL3MBTL1ATM
SCHEMBL11975945 0.84 ALDH1A1 (0.35) ALDH1A1MEN1KMT2ATSHRL3MBTL1
SCHEMBL393307 0.83 ALDH1A1 (0.38) ALDH1A1MEN1KMT2ATSHRL3MBTL1

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 17 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240294498-A1 FACTOR XIIA INHIBITORS LUNAC THERAPEUTICS LTD (GB) 2024-09-05 US disclosed
CN-118043316-A Factor XIIa inhibitors 卢纳克治疗有限公司 2024-05-14 CN disclosed
US-11654197-B2 Pyrrolobenzodiazepine dimer prodrug and ligand-linker conjugate compound of the same LEGOCHEM BIOSCIENCES, INC. (KR) 2023-05-23 US disclosed
WO-2022248883-A1 FACTOR XIIA INHIBITORS LUNAC THERAPEUTICS LTD (GB) 2022-12-01 WO disclosed
US-20220218830-A1 PYRROLOBENZODIAZEPINE DIMER PRODRUG AND LIGAND-LINKER CONJUGATE COMPOUND OF THE SAME LIGACHEM BIOSCIENCES INC. (KR) 2022-07-14 US disclosed
US-9981960-B2 Pyrrolidine compound and application as melanocortin receptor agonist MITSUBISHI TANABE PHARMA CORPORATION (JP) 2018-05-29 US disclosed
US-9981960-B2 Pyrrolidine compound and application as melanocortin receptor agonist MITSUBISHI TANABE PHARMA CORPORATION (JP) 2018-05-29 US disclosed
US-20170190697-A1 NOVEL PYRROLIDINE COMPOUND AND APPLICATION AS MELANOCORTIN RECEPTOR AGONIST MITSUBISHI TANABE PHARMA CORPORATION (JP) 2017-07-06 US disclosed
US-20170190697-A1 NOVEL PYRROLIDINE COMPOUND AND APPLICATION AS MELANOCORTIN RECEPTOR AGONIST MITSUBISHI TANABE PHARMA CORPORATION (JP) 2017-07-06 US disclosed
US-8299021-B2 Macrocyclic inhibitors of hepatitis C virus replication INTERMUNE, INC. (US) 2012-10-30 US disclosed
US-20120208995-A1 NOVEL MACROCYCLIC INHIBITORS OF HEPATITIS C VIRUS REPLICATION ARRAY BIOPHARMA, INC. (US) 2012-08-16 US disclosed
US-7829665-B2 Macrocyclic inhibitors of hepatitis C virus replication INTERMUNE, INC. (US) 2010-11-09 US disclosed
US-20090169510-A1 NOVEL MACROCYCLIC INHIBITORS OF HEPATITIS C VIRUS REPLICATION INTERMUNE, INC. (US) 2009-07-02 US disclosed
US-20090148407-A1 Novel Macrocyclic Inhibitors of Hepatitis C Virus Replication INTERMUNE, INC. (US) 2009-06-11 US disclosed
US-20070054842-A1 Novel macrocyclic inhibitors of hepatitis C virus replication ARRAY BIOPHARMA, INC. 2007-03-08 US disclosed
US-20030216374-A1 Antibiotic oxazolidinone derivatives SYNGENTA LIMITED (GB) 2003-11-20 US disclosed
US-6605630-B1 Active against drug resistant gram positive pathogens SYNGENTA LIMITED (GB) 2003-08-12 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 (9 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-20220218830-A1 PYRROLOBENZODIAZEPINE DIMER PRODRUG AND LIGAND-LINKER CONJUGATE COMPOUND OF THE SAME GABRP, GABRD, GABBR2 ALDH1A1 1783/4885MEN1 3471/4885KMT2A 1332/4885
US-20090169510-A1 NOVEL MACROCYCLIC INHIBITORS OF HEPATITIS C VIRUS REPLICATION EIF2AK2, HAVCR2, HCCS ALDH1A1 2539/4885MEN1 4454/4885KMT2A 3154/4885
US-20070054842-A1 Novel macrocyclic inhibitors of hepatitis C virus replication EIF2AK2, HAVCR2, HCCS ALDH1A1 2539/4885MEN1 4454/4885KMT2A 3154/4885
US-20170190697-A1 NOVEL PYRROLIDINE COMPOUND AND APPLICATION AS MELANOCORTIN RECEPTOR AGONIST MC1R, MC5R, MC3R ALDH1A1 1837/4885MEN1 987/4885KMT2A 793/4885
US-20120208995-A1 NOVEL MACROCYCLIC INHIBITORS OF HEPATITIS C VIRUS REPLICATION EIF2AK2, HAVCR2, HCCS ALDH1A1 2539/4885MEN1 4454/4885KMT2A 3154/4885
US-20240294498-A1 FACTOR XIIA INHIBITORS F11, F13B, F7 ALDH1A1 3635/4885MEN1 1335/4885KMT2A 3026/4885
US-20090148407-A1 Novel Macrocyclic Inhibitors of Hepatitis C Virus Replication EIF2AK2, HAVCR2, HCCS ALDH1A1 2173/4885MEN1 4409/4885KMT2A 2949/4885
US-11654197-B2 Pyrrolobenzodiazepine dimer prodrug and ligand-linker conjugate compound of the same GABRP, GABRD, GABBR2 ALDH1A1 1783/4885MEN1 3471/4885KMT2A 1332/4885
US-20030216374-A1 Antibiotic oxazolidinone derivatives OXA1L, HRH1, OGDH ALDH1A1 1208/4885MEN1 3613/4885KMT2A 3384/4885

“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.