SCHEMBL307099

SCHEMBL307099

CC(C)(C)OC(=O)N1CCOC[C@@H]1CO

nearest known ligand 0.49

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
▸ PDK1 Q15118 4/20 0.49
▸ USP2 O75604 1/20 0.49
▸ SMN1; SMN2 Q16637 1/20 0.49
▸ RECQL P46063 1/20 0.43
▸ ATM Q13315 2/20 0.41
▸ NR1H2 P55055 1/20 0.40
▸ IL1B P01584 1/20 0.39
▸ P2RX7 Q99572 1/20 0.39
▸ PDK2 Q15119 1/20 0.38
▸ PDK3 Q15120 1/20 0.38
▸ CTSD P07339 1/20 0.35
▸ CTSL P07711 1/20 0.35
▸ CTSB P07858 1/20 0.35
▸ CTSS P25774 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
SCHEMBL305110 1.00 PDK1 (0.49) PDK1USP2SMN1; SMN2RECQLATM
SCHEMBL1184919 1.00 PDK1 (0.49) PDK1USP2SMN1; SMN2RECQLATM
SCHEMBL31148538 0.91 SMN1; SMN2 (0.43) PDK1USP2SMN1; SMN2RECQLATM
SCHEMBL30789316 0.91 SMN1; SMN2 (0.43) PDK1USP2SMN1; SMN2RECQLATM
SCHEMBL4223343 0.88 USP2 (0.46) PDK1USP2SMN1; SMN2RECQLATM
SCHEMBL11995203 0.88 USP2 (0.46) PDK1USP2SMN1; SMN2RECQLATM
SCHEMBL18914800 0.88 USP2 (0.46) PDK1USP2SMN1; SMN2RECQLATM
SCHEMBL14417217 0.88 USP2 (0.49) PDK1USP2SMN1; SMN2RECQLATM
SCHEMBL3641031 0.88 USP2 (0.49) PDK1USP2SMN1; SMN2RECQLATM
SCHEMBL20371626 0.88 USP2 (0.49) PDK1USP2SMN1; SMN2RECQLATM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3959211-B1 4H-PYRROLO[3,2-C]PYRIDIN-4-ONE COMPOUNDS BAYER AG (DE) 2026-02-18 — — EP disclosed
EP-4689155-A1 USE OF INHIBITORS TO INCREASE EFFICIENCY OF CRISPR/CAS INSERTIONS Astrazeneca AB (SE) 2026-02-11 — — EP disclosed
US-12492197-B2 3,5-disubstituted pyrazole compounds as kinase inhibitors and uses thereof Impact Therapeutics (Shanghai), Inc (CN) 2025-12-09 — — US disclosed
EP-4630410-A1 POLQ INHIBITORS Astrazeneca AB (SE) 2025-10-15 — — EP disclosed
US-12414954-B2 POLQ inhibitors ASTRAZENECA AB (SE) 2025-09-16 — — US disclosed
US-20250195530-A1 POLQ INHIBITORS ASTRAZENECA AB (SE) 2025-06-19 — — US disclosed
US-20250171402-A1 Potent and Selective Human Neuronal Nitric Oxide Synthase Inhibitors UNIV NORTHWESTERN (US) 2025-05-29 — — US disclosed
US-20250136599-A1 4H-PYRROLO[3,2-C]PYRIDIN-4-ONE COMPOUNDS BAYER AKTIENGESELLSCHAFT (DE) 2025-05-01 — — US disclosed
US-20250127801-A1 BRIDGED TRICYCLIC CARBAMOYLPYRIDONE COMPOUNDS AND USES THEREOF GILEAD SCIENCES, INC. 2025-04-24 — — US disclosed
EP-3853234-B1 FUSED TRICYCLIC RING DERIVATIVES AS SRC HOMOLOGY-2 PHOSPHATASE INHIBITORS NIKANG THERAPEUTICS INC (US) 2025-04-23 — — EP disclosed
WO-2006105262-A1 HETEROARYL UREA DERIVATIVES USEFUL FOR INHIBITING CHKl ICOS CORPORATION (US) 2006-10-05 — — WO disclosed
EP-1699798-A2 DI-SUBSTITUTED PYRROLOTRIAZINE COMPOUNDS Bristol-Myers Squibb Company (US) 2006-09-13 — — EP disclosed
US-7064203-B2 Di-substituted pyrrolotriazine compounds BRISTOL MYERS SQUIBB COMPANY (US) 2006-06-20 — — US disclosed
US-20050222153-A1 C-6 modified indazolylpyrrolotriazines VITE GREGORY D 2005-10-06 — — US disclosed
US-20050197339-A1 Di-substituted pyrrolotrizine compounds BRISTOL-MYERS SQUIBB COMPANY 2005-09-08 — — US disclosed
WO-2005065266-A2 DI-SUBSTITUTED PYRROLOTRIAZINE COMPOUNDS BRISTOL-MYERS SQUIBB COMPANY (US) 2005-07-21 — — WO disclosed
US-6916815-B2 C-6 modified indazolylpyrrolotriazines BRISTOL-MYERS SQUIBB COMPANY (US) 2005-07-12 — — US disclosed
US-20040142931-A1 C-6 modified indazolylpyrrolotriazines BRISTOL-MYERS SQUIBB COMPANY 2004-07-22 — — US disclosed
US-6221865-B1 INHIBITORS OF PROTEIN FARNESYLTRANSFERASE AND PROTEIN GERANYLGERANYLTRANSFERASE. UNIVERSITY OF PITTSBURGH 2001-04-24 — — US disclosed
WO-1998050030-A1 INHIBITORS OF PROTEIN ISOPRENYL TRANSFERASES UNIVERSITY OF PITTSBURGH (US) 1998-11-12 — — 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 (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-12492197-B2 3,5-disubstituted pyrazole compounds as kinase inhibitors and uses thereof CHEK1, CHEK2, CCNK PDK1 316/4885USP2 1684/4885SMN1; SMN2 4202/4885
US-20050222153-A1 C-6 modified indazolylpyrrolotriazines ERBB2, ERBB4, EGFR PDK1 890/4885USP2 4240/4885SMN1; SMN2 4572/4885
US-12414954-B2 POLQ inhibitors POLQ, POLG, POLB PDK1 2002/4885USP2 3499/4885SMN1; SMN2 2586/4885
US-20050197339-A1 Di-substituted pyrrolotrizine compounds ERBB2, ERBB4, EGFR PDK1 145/4885USP2 4352/4885SMN1; SMN2 4784/4885
US-20250136599-A1 4H-PYRROLO[3,2-C]PYRIDIN-4-ONE COMPOUNDS CYP4B1, CYP2C19, PAH PDK1 179/4885USP2 4225/4885SMN1; SMN2 407/4885
US-20250127801-A1 BRIDGED TRICYCLIC CARBAMOYLPYRIDONE COMPOUNDS AND USES THEREOF SDHA, SDHB, DPYD PDK1 128/4885USP2 3590/4885SMN1; SMN2 2987/4885
US-20250171402-A1 Potent and Selective Human Neuronal Nitric Oxide Synthase Inhibitors NOS2, NOS1, NOS3 PDK1 1744/4885USP2 2470/4885SMN1; SMN2 71/4885
US-20250195530-A1 POLQ INHIBITORS POLQ, POLG, POLB PDK1 2002/4885USP2 3499/4885SMN1; SMN2 2586/4885
US-20040142931-A1 C-6 modified indazolylpyrrolotriazines ERBB2, ERBB4, EGFR PDK1 907/4885USP2 4320/4885SMN1; SMN2 4567/4885

“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.

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