SCHEMBL2896952

SCHEMBL2896952

CC1(CO)CCCN(C(=O)OC(C)(C)C)C1

nearest known ligand 0.42

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
HPGD P15428 1/20 0.42
USP2 O75604 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
NR1H2 P55055 1/20 0.40
MEN1 O00255 2/20 0.39
KMT2A Q03164 2/20 0.39
ALDH1A1 P00352 1/20 0.39
MAPT P10636 1/20 0.39
VNN1 O95497 1/20 0.38
CTSK P43235 1/20 0.38
EPHX1 P07099 1/20 0.38
PIK3R1 P27986 3/20 0.37
PIK3CA P42336 3/20 0.37
MMP2 P08253 1/20 0.37
MMP13 P45452 1/20 0.37
MMP14 P50281 1/20 0.37
ADAM17 P78536 1/20 0.37
RORC P51449 1/20 0.37
SCD5 Q86SK9 1/20 0.37

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
SCHEMBL31387757 1.00 HPGD (0.42) HPGDUSP2SMN1; SMN2NR1H2MEN1
SCHEMBL320729 0.91 USP2 (0.44) HPGDUSP2SMN1; SMN2NR1H2RORC
SCHEMBL29719128 0.91 USP2 (0.44) HPGDUSP2SMN1; SMN2NR1H2RORC
SCHEMBL19637316 0.91 USP2 (0.44) HPGDUSP2SMN1; SMN2NR1H2RORC
SCHEMBL21664406 0.88 HPGD (0.42) HPGDUSP2SMN1; SMN2NR1H2MEN1
SCHEMBL12179888 0.88 HPGD (0.42) HPGDUSP2SMN1; SMN2NR1H2MEN1
SCHEMBL26667346 0.88 HPGD (0.46) HPGDUSP2SMN1; SMN2NR1H2MEN1
SCHEMBL2897254 0.87 HPGD (0.41) HPGDUSP2SMN1; SMN2NR1H2MEN1
SCHEMBL28914034 0.87 HPGD (0.41) HPGDUSP2SMN1; SMN2NR1H2MEN1
SCHEMBL17386554 0.86 HPGD (0.43) HPGDUSP2SMN1; SMN2NR1H2MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4747239-A1 SMALL MOLECULE PROTEIN DEGRADERS OF KRAS G12D MUTANT Merck Sharp & Dohme LLC (US) 2026-05-27 EP disclosed
CN-122079960-A Alkynyl quinazoline compounds 2026-05-26 CN disclosed
US-20260116881-A1 KIF MODULATOR COMPOUNDS AND METHODS OF USE IAMBIC THERAPEUTICS INC (US) 2026-04-30 US disclosed
EP-4013749-B1 ALKYNYL QUINAZOLINE COMPOUNDS BLACK DIAMOND THERAPEUTICS INC (US) 2026-03-11 EP disclosed
US-20260049063-A1 ALKYNYL QUINAZOLINE COMPOUNDS BLACK DIAMOND THERAPEUTICS INC (US) 2026-02-19 US disclosed
US-12435046-B2 Alkynyl quinazoline compounds BLACK DIAMOND THERAPEUTICS, INC. (US) 2025-10-07 US disclosed
CN-119390683-A Alkynyl quinazoline compounds 黑钻治疗公司 2025-02-07 CN disclosed
WO-2025019823-A1 SMALL MOLECULE PROTEIN DEGRADERS OF KRAS G12D MUTANT MERCK SHARP & DOHME LLC (US) 2025-01-23 WO disclosed
CN-118525018-A Bialkyne compound and application thereof 上海艾力斯医药科技股份有限公司 2024-08-20 CN disclosed
US-20240150362-A1 Substituted Pyrrolotriazines MOLECURE S.A. (PL) 2024-05-09 US disclosed
US-20060217376-A1 Therapeutic pyrazolo[3,4-b]pyridines and indazoles WARNER-LAMBERT COMPANY LLC 2006-09-28 US disclosed
US-20060205676-A1 Pyridine derivatives BAYER AKTIENGESELLSCHAFT (DE) 2006-09-14 US disclosed
WO-2006056873-A2 THERAPEUTIC PYRAZOLO[3,4-B] PYRIDINES AND INDAZOLES WARNER-LAMBERT COMPANY LLC (US) 2006-06-01 WO disclosed
US-20060116376-A1 Therapeutic pyrazolo[3,4-B]pyridines and indazoles WARNER-LAMBERT COMPANY LLC 2006-06-01 US disclosed
US-20060100246-A1 Pyridine derivatives BAYER AKTIENGESELLSCHAFT (DE) 2006-05-11 US disclosed
US-6984649-B1 Pyridine derivatives BAYER AKTIENGESELLSCHAFT (DE) 2006-01-10 US disclosed
CN-1476442-A Pyridine derivatives with IKB-kinase (IKK-beta) INhibiting activity 2004-02-18 CN disclosed
EP-1326856-A1 PYRIDINE DERIVATIVES WITH IKB-KINASE (IKK-BETA) INHIBITING ACTIVITY Bayer Aktiengesellschaft (DE) 2003-07-16 EP disclosed
US-6562811-B1 Inhibit I kappa B kinase beta (IKK- beta or IKK-beta) activity, thus inhibit nuclear factor kappa B (NF- kappa B) and can be used for the prophylaxis and treatment of inflammation BAYER AKTIENGESELLSCHAFT (DE) 2003-05-13 US disclosed
WO-2002024679-A1 PYRIDINE DERIVATIVES WITH IKB-KINASE (IKK-β) INHIBITING ACTIVITY BAYER AKTIENGESELLSCHAFT (DE) 2002-03-28 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 (8 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-20260116881-A1 KIF MODULATOR COMPOUNDS AND METHODS OF USE KIF2C, KIF5B, KIF5C HPGD 4099/4885USP2 2094/4885SMN1; SMN2 218/4885
US-12435046-B2 Alkynyl quinazoline compounds GLS, GLS2, MCL1 HPGD 2164/4885USP2 2868/4885SMN1; SMN2 206/4885
US-20240150362-A1 Substituted Pyrrolotriazines USP7, UBA7, USP5 HPGD 2822/4885USP2 4/4885SMN1; SMN2 2350/4885
US-20060205676-A1 Pyridine derivatives CBR3, ARG1, HRH3 HPGD 1115/4885USP2 3458/4885SMN1; SMN2 4372/4885
US-20060100246-A1 Pyridine derivatives NAPRT, NNT, NANS HPGD 224/4885USP2 4128/4885SMN1; SMN2 3547/4885
US-20060116376-A1 Therapeutic pyrazolo[3,4-B]pyridines and indazoles P2RX3, P2RX4, ACHE HPGD 1782/4885USP2 3597/4885SMN1; SMN2 314/4885
US-20060217376-A1 Therapeutic pyrazolo[3,4-b]pyridines and indazoles P2RX3, P2RX4, ACHE HPGD 1782/4885USP2 3597/4885SMN1; SMN2 314/4885
US-20260049063-A1 ALKYNYL QUINAZOLINE COMPOUNDS H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, MCL1, BCL6 HPGD 4394/4885USP2 3743/4885SMN1; SMN2 793/4885

“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.