SCHEMBL6802979

SCHEMBL6802979

CC(C)(C)OC(=O)NCC12CCC(C#N)(CC1)CC2

nearest known ligand 0.40

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
CTSL P07711 2/20 0.40
MEN1 O00255 2/20 0.39
KMT2A Q03164 2/20 0.39
ALDH1A1 P00352 1/20 0.39
TSHR P16473 1/20 0.39
HCRTR2 O43614 1/20 0.39
CTSS P25774 8/20 0.38
CTSK P43235 8/20 0.38
CA12 O43570 2/20 0.38
CA1 P00915 2/20 0.38
CA2 P00918 2/20 0.38
CA9 Q16790 2/20 0.38
TDP1 Q9NUW8 1/20 0.37
MAOA P21397 1/20 0.36
MAOB P27338 1/20 0.36
CTSB P07858 1/20 0.36
GAA P10253 1/20 0.36
EPHX1 P07099 1/20 0.35

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
SCHEMBL8255697 0.81 TDP1 (0.45) MEN1KMT2AALDH1A1TSHRHCRTR2
SCHEMBL22604487 0.81 MEN1 (0.42) MEN1KMT2AALDH1A1TSHRHCRTR2
SCHEMBL8253836 0.81 HCRTR2 (0.42) CTSLMEN1KMT2AALDH1A1TSHR
SCHEMBL8256590 0.80 HCRTR2 (0.41) MEN1KMT2AALDH1A1TSHRHCRTR2
SCHEMBL8230389 0.80 HCRTR2 (0.41) MEN1KMT2AALDH1A1TSHRHCRTR2
SCHEMBL25317380 0.80 CTSL (0.43) CTSLMEN1KMT2AALDH1A1TSHR
SCHEMBL31432022 0.80 HCRTR2 (0.41) CTSLMEN1KMT2AALDH1A1TSHR
SCHEMBL22604486 0.80 HCRTR2 (0.41) MEN1KMT2AALDH1A1TSHRHCRTR2
SCHEMBL27343898 0.80 HCRTR2 (0.41) CTSLMEN1KMT2AALDH1A1TSHR
SCHEMBL10163707 0.78 HCRTR2 (0.40) CTSLMEN1KMT2AALDH1A1TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4634169-A1 3-FLUORO-4-HYDROXYBENZMIDE-CONTAINING INHIBITORS AND/OR DEGRADERS AND USES THEREOF Pfizer Inc. (US) 2025-10-22 EP disclosed
US-20240238425-A1 HSD17B13 Inhibitors and/or Degraders PFIZER INC. (US) 2024-07-18 US disclosed
WO-2024127297-A1 3-FLUORO-4-HYDROXYBENZMIDE-CONTAINING INHIBITORS AND/OR DEGRADERS AND USES THEREOF PFIZER INC. (US) 2024-06-20 WO disclosed
US-20240150334-A1 HSD17B13 INHIBITORS AND/OR DEGRADERS PFIZER INC. (US) 2024-05-09 US disclosed
US-8835441-B2 Heterobicyclic metalloprotease inhibitors AMGEN INC. (US) 2014-09-16 US disclosed
US-20120015920-A1 HETEROBICYCLIC METALLOPROTEASE INHIBITORS ALANTOS PHARMACEUTICALS HOLDING, INC. (US) 2012-01-19 US disclosed
US-20120015920-A1 HETEROBICYCLIC METALLOPROTEASE INHIBITORS ALANTOS PHARMACEUTICALS HOLDING, INC. (US) 2012-01-19 US disclosed
US-7795245-B2 Heterobicyclic metalloprotease inhibitors Atlantos Pharmaceuticals Holding, Inc. (US) 2010-09-14 US disclosed
US-7795245-B2 Heterobicyclic metalloprotease inhibitors Atlantos Pharmaceuticals Holding, Inc. (US) 2010-09-14 US disclosed
US-20090312312-A1 Heterobicyclic Metalloprotease Inhibitors ALANTOS PHARMACEUTICALS HOLDING, INC. (US) 2009-12-17 US disclosed
US-20070155738-A1 Heterobicyclic metalloprotease inhibitors ALANTOS PHARMACEUTICALS, INC. 2007-07-05 US disclosed
US-20070155738-A1 Heterobicyclic metalloprotease inhibitors ALANTOS PHARMACEUTICALS, INC. 2007-07-05 US disclosed
US-20040058857-A1 Method of treating cancer YAO SIU-LONG (US) 2004-03-25 US disclosed
EP-1009420-B1 CONJUGATES USEFUL IN THE TREATMENT OF PROSTATE CANCER MERCK & CO INC (US) 2003-12-17 EP disclosed
US-20030220241-A1 Method of treating cancer DEFEO-JONES DEBORAH (US) 2003-11-27 US disclosed
US-20030215456-A1 Method of treating cancer YAO SUI-LONG (US) 2003-11-20 US disclosed
US-20020173451-A1 Method of treating cancer YAO SUI-LONG (US) 2002-11-21 US disclosed
US-20020041880-A1 Method of treating cancer DEFEO-JONES DEBORAH (US) 2002-04-11 US disclosed
US-20020042375-A1 Method of treating cancer HEIMBROOK DAVID C (US) 2002-04-11 US disclosed
US-6127333-A COMPRISING OLIGOPEPTIDES, HAVING AMINO ACID SEQUENCES THAT ARE SELECTIVELY PROTEOLYTICALLY CLEAVED BY FREE PROSTATE SPECIFIC ANTIGEN AND KNOWN CYTOTOXIC AGENTS, CHARACTERIZED BY A DIAMINE LINKER BETWEEN THE OLIGOPEPTIDE AND VINBLASTINE MERCK & CO., INC. (US) 2000-10-03 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 (11 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-20030220241-A1 Method of treating cancer ACP3, PSAT1, LCAT CTSL 973/4885MEN1 783/4885KMT2A 1240/4885
US-20240238425-A1 HSD17B13 Inhibitors and/or Degraders HSD17B13, HSD17B3, HSD17B1 CTSL 2803/4885MEN1 4182/4885KMT2A 1081/4885
US-20020042375-A1 Method of treating cancer ACP3, KLK3, FOLH1 CTSL 770/4885MEN1 707/4885KMT2A 2337/4885
US-20040058857-A1 Method of treating cancer KLK3, SHBG, ACP3 CTSL 859/4885MEN1 276/4885KMT2A 1984/4885
US-20240150334-A1 HSD17B13 INHIBITORS AND/OR DEGRADERS HSD17B1, HSD17B3, HSD17B13 CTSL 1793/4885MEN1 3752/4885KMT2A 2873/4885
US-20090312312-A1 Heterobicyclic Metalloprotease Inhibitors MMP13, TIMP3, MMP3 CTSL 63/4885MEN1 3090/4885KMT2A 3548/4885
US-20120015920-A1 HETEROBICYCLIC METALLOPROTEASE INHIBITORS MMP13, TIMP3, MMP3 CTSL 63/4885MEN1 3090/4885KMT2A 3548/4885
US-20030215456-A1 Method of treating cancer TACR1, TACR2, KLK3 CTSL 433/4885MEN1 521/4885KMT2A 995/4885
US-20020173451-A1 Method of treating cancer FOLH1, KLK3, ACP3 CTSL 175/4885MEN1 993/4885KMT2A 1907/4885
US-20070155738-A1 Heterobicyclic metalloprotease inhibitors MMP13, TIMP3, MMP3 CTSL 63/4885MEN1 3090/4885KMT2A 3548/4885
US-20020041880-A1 Method of treating cancer ACP3, FOLH1, KLK3 CTSL 623/4885MEN1 859/4885KMT2A 1771/4885

“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.