SCHEMBL344915

SCHEMBL344915

CC(C)(C)OC(=O)N1CCCC(CO)C1

nearest known ligand 0.59

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
NR1H2 P55055 1/20 0.59
MEN1 O00255 1/20 0.56
ALDH1A1 P00352 1/20 0.56
MAPT P10636 1/20 0.56
KMT2A Q03164 1/20 0.56
GLS O94925 2/20 0.50
HPGD P15428 1/20 0.50
BACE1 P56817 2/20 0.48
ACKR3 P25106 1/20 0.48
CTSD P07339 1/20 0.48
KDM1A O60341 1/20 0.46
FEN1 P39748 1/20 0.46
SCN9A Q15858 1/20 0.46
EPHX1 P07099 1/20 0.44
EPHX2 P34913 2/20 0.44
CYP2C9 P11712 1/20 0.44
GRM3 Q14832 2/20 0.43

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
SCHEMBL344916 1.00 NR1H2 (0.59) NR1H2MEN1ALDH1A1MAPTKMT2A
SCHEMBL1785894 1.00 NR1H2 (0.59) NR1H2MEN1ALDH1A1MAPTKMT2A
SCHEMBL31421369 0.95 NR1H2 (0.57) NR1H2MEN1ALDH1A1MAPTKMT2A
SCHEMBL31421589 0.95 NR1H2 (0.57) NR1H2MEN1ALDH1A1MAPTKMT2A
SCHEMBL2071987 0.95 NR1H2 (0.57) NR1H2MEN1ALDH1A1MAPTKMT2A
SCHEMBL7448268 0.93 NR1H2 (0.52) NR1H2MEN1ALDH1A1MAPTKMT2A
SCHEMBL514696 0.90 NR1H2 (0.62) NR1H2MEN1ALDH1A1MAPTKMT2A
SCHEMBL515486 0.90 NR1H2 (0.62) NR1H2MEN1ALDH1A1MAPTKMT2A
SCHEMBL621267 0.90 NR1H2 (0.62) NR1H2MEN1ALDH1A1MAPTKMT2A
SCHEMBL16863978 0.90 NR1H2 (0.58) NR1H2MEN1ALDH1A1MAPTKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109988098-A The synthetic method of one kind (R)-N- tertbutyloxycarbonyl -3- hydroxymethyl piperidine 常州工程职业技术学院 2019-07-09 CN claimed
US-20080306096-A1 Quinazoline Derivatives, Process for Their Preparation and Their Use as Anti-Cancer Agents ASTRAZENECA AB (SE) 2008-12-11 US claimed
US-20260137703-A1 2-AMINO-PYRIDO[2,3-D]PYRIMIDIN-7(8H)-ONE AND 7-AMINO-1-PYRIMIDO[4,5-D]PYRIMIDIN-2(1 H)-ONE DERIVATIVES AS EGFR INHIBITORS FOR THE TREATMENT OF CANCER CANCER RESEARCH TECH LIMITED (GB) 2026-05-21 US disclosed
EP-3364967-B1 FERROPORTIN INHIBITORS VIFOR INT AG (CH) 2026-05-20 EP disclosed
US-12630551-B2 Endocyclic pyrimidinone compounds, and preparation methods, compositions and use thereof NEUSCO BIOTECH LIMITED (CN) 2026-05-19 US disclosed
US-20260116881-A1 KIF MODULATOR COMPOUNDS AND METHODS OF USE IAMBIC THERAPEUTICS INC (US) 2026-04-30 US disclosed
US-12612380-B2 Non-lysosomal glucosylceramidase inhibitors and uses thereof ALECTOS THERAPEUTICS 1NC (CA) 2026-04-28 US disclosed
EP-3966199-B1 NON-LYSOSOMAL GLUCOSYLCERAMIDASE INHIBITORS AND USES THEREOF ALECTOS THERAPEUTICS INC (CA) 2026-03-18 EP disclosed
US-12570672-B2 Macrocyclic compounds and methods of use AMGEN INC. 2026-03-10 US disclosed
EP-4695238-A1 CDK2 INHIBITORS Blueprint Medicines Corporation (US) 2026-02-18 EP disclosed
EP-4695259-A1 TRICYCLIC COMPOUNDS FOR TREATMENT OF BACTERIAL INFECTIONS F. Hoffmann-La Roche AG (CH) 2026-02-18 EP disclosed
WO-1994013291-A1 USE OF ARYLOXYALKYL SUBSTITUTED CYCLIC AMINES AS CALCIUM CHANNEL ANTAGONISTS AND NEW PHENYLOXYALKYL PIPERIDIN DERIVATIVES SMITHKLINE BEECHAM PLC (GB) 1994-06-23 WO disclosed
EP-0601459-A2 Sulfonamido heterocyclic thrombin inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 1994-06-15 EP disclosed
WO-1994011382-A1 ANTINEOPLASTIC HETERONAPHTHOQUINONES BIOCHEM PHARMA INC. (CA) 1994-05-26 WO disclosed
US-5260307-A Inhibit thrombin-induced platlet aggregation and clotting of fibrogen in plasma HOFMANN-LA ROCHE INC. (US) 1993-11-09 US disclosed
EP-0559046-A1 N-amidinopiperidinyl(3/4)- or N-amidino-1,4-Oxazinyl(2)-substituted sulfonamides, process for their preparation and use as thrombin inhibitors F.HOFFMANN-LA ROCHE & CO. AKTIENGESELLSCHAFT (CH) 1993-09-08 EP disclosed
EP-0495750-A2 Heterocyclic hydroxylamine CIBA-GEIGY AG (CH) 1992-07-22 EP disclosed
EP-0468231-A2 Guanidins F. HOFFMANN-LA ROCHE AG (CH) 1992-01-29 EP disclosed
US-4987132-A PLATELET ACTIVATING FACTOR ANTAGONISTS YAMANOUCHI PHARMACEUTICAL CO., LTD. (JP) 1991-01-22 US disclosed
EP-0279681-A2 Saturated heterocyclic carboxamide derivatives YAMANOUCHI PHARMACEUTICAL CO. LTD. (JP) 1988-08-24 EP 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 (6 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 NR1H2 745/4885MEN1 4063/4885ALDH1A1 2556/4885
US-20260137703-A1 2-AMINO-PYRIDO[2,3-D]PYRIMIDIN-7(8H)-ONE AND 7-AMINO-1-PYRIMIDO[4,5-D]PYRIMIDIN-2(1 H)-ONE DERIVATIVES AS EGFR INHIBITORS FOR THE TREATMENT OF CANCER EGFR, KRAS, O60361 NR1H2 2747/4885MEN1 3020/4885ALDH1A1 999/4885
US-20080306096-A1 Quinazoline Derivatives, Process for Their Preparation and Their Use as Anti-Cancer Agents BRAF, RAF1, NRAS NR1H2 4110/4885MEN1 568/4885ALDH1A1 1302/4885
US-12570672-B2 Macrocyclic compounds and methods of use KRAS, NRAS, BRAF NR1H2 2728/4885MEN1 34/4885ALDH1A1 3351/4885
US-12630551-B2 Endocyclic pyrimidinone compounds, and preparation methods, compositions and use thereof LPAR1, PLA2R1, LPAR2 NR1H2 57/4885MEN1 4367/4885ALDH1A1 1113/4885
US-12612380-B2 Non-lysosomal glucosylceramidase inhibitors and uses thereof GBA1, GBA2, MAN2B1 NR1H2 908/4885MEN1 3585/4885ALDH1A1 1393/4885

“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.