SCHEMBL1721997

SCHEMBL1721997

CCOC(=O)C[C@H]1CC[C@H](CO)CC1

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MGAM O43451 1/20 0.43
GAA P10253 1/20 0.43
SI P14410 1/20 0.43
MGAM2 Q2M2H8 1/20 0.43
ALDH1A1 P00352 5/20 0.40
TRPA1 O75762 1/20 0.40
JAK2 O60674 1/20 0.38
JAK1 P23458 1/20 0.38
TYK2 P29597 1/20 0.38
JAK3 P52333 1/20 0.38
TDP1 Q9NUW8 2/20 0.37
KMT2A Q03164 2/20 0.37
MEN1 O00255 1/20 0.36
POLB P06746 1/20 0.36
CA12 O43570 1/20 0.36
CA1 P00915 1/20 0.36
CA2 P00918 1/20 0.36
CA9 Q16790 1/20 0.36
CYP1A2 P05177 1/20 0.35
L3MBTL1 Q9Y468 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
SCHEMBL18971858 1.00 MGAM (0.43) MGAMGAASIMGAM2ALDH1A1
SCHEMBL1057822 1.00 MGAM (0.43) MGAMGAASIMGAM2ALDH1A1
SCHEMBL2721040 0.92
SCHEMBL14389976 0.86 MGAM (0.44) MGAMGAASIMGAM2ALDH1A1
SCHEMBL14389978 0.86 MGAM (0.44) MGAMGAASIMGAM2ALDH1A1
SCHEMBL7790319 0.85 MGAM (0.40) MGAMGAASIMGAM2ALDH1A1
SCHEMBL21072260 0.84 MGAM (0.43) MGAMGAASIMGAM2ALDH1A1
SCHEMBL7782689 0.84 MGAM (0.43) MGAMGAASIMGAM2ALDH1A1
SCHEMBL3036111 0.84 MGAM (0.43) MGAMGAASIMGAM2ALDH1A1
SCHEMBL12353793 0.84 MGAM (0.43) MGAMGAASIMGAM2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250236632-A1 BETA-LACTAMASE INHIBITORS VENATORX PHARMACEUTICALS INC (US) 2025-07-24 US disclosed
EP-3922635-A1 BETA-LACTAMASE INHIBITORS Venatorx Pharmaceuticals, Inc. (US) 2021-12-15 EP disclosed
EP-2928898-B1 BETA-LACTAMASE INHIBITORS VENATORX PHARMACEUTICALS INC (US) 2021-04-14 EP disclosed
US-10669290-B2 Beta-lactamase inhibitors VenatoRx Pharmaceuticals, Inc. (US) 2020-06-02 US disclosed
EP-3388423-B1 NK1 RECEPTOR ANTAGONIST KISSEI PHARMACEUTICAL (JP) 2020-05-27 EP disclosed
US-10399949-B2 NK1 receptor antagonist KISSEI PHARMACEUTICAL CO., LTD. (JP) 2019-09-03 US disclosed
US-20190225628-A1 BETA-LACTAMASE INHIBITORS NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2019-07-25 US disclosed
US-20190002414-A1 NK1 RECEPTOR ANTAGONIST KISSEI PHARMACEUTICAL CO., LTD. (JP) 2019-01-03 US disclosed
US-20180194783-A1 BETA-LACTAMASE INHIBITORS VenatoRx Pharmaceuticals, Inc. 2018-07-12 US disclosed
US-9828391-B2 Beta-lactamase inhibitors VenatoRx Pharmaceuticals, Inc. (US) 2017-11-28 US disclosed
US-8759365-B2 Organic compounds NOVARTIS AG (CH) 2014-06-24 US disclosed
US-20140171390-A1 BETA-LACTAMASE INHIBITORS VenatoRx Pharmaceuticals, Inc. (US) 2014-06-19 US disclosed
WO-2014089365-A1 BETA-LACTAMASE INHIBITORS VENATORX PHARMACEUTICALS, INC (US) 2014-06-12 WO disclosed
CN-101878199-B 1,2-disubstituted-4-benzylamino-pyrrolidine derivatives as cetp inhibitors useful for the treatment of diseases such as hyperli pidemia or arteriosclerosis NOVARTIS AG 2013-09-18 CN disclosed
EP-2404901-A1 1,2-Disubstituted 4-benzylamino-pyrrolidine derivatives as CETP inhibitors useful for the treatment of diseases such as hyperlipidemia or arteriosclerosis Novartis AG (CH) 2012-01-11 EP disclosed
EP-2229356-B1 1,2-DISUBSTITUTED-4-BENZYLAMINO-PYRROLIDINE DERIVATIVES AS CETP INHIBITORS USEFUL FOR THE TREATMENT OF DISEASES SUCH AS HYPERLI PIDEMIA OR ARTERIOSCLEROSIS NOVARTIS AG (CH) 2011-10-12 EP disclosed
US-20100311750-A1 ORGANIC COMPOUNDS NOVARTIS AG (CH) 2010-12-09 US disclosed
CN-101878199-A 1,2-disubstituted-4-benzylamino-pyrrolidine derivatives as cetp inhibitors useful for the treatment of diseases such as hyperli pidemia or arteriosclerosis NOVARTIS AG 2010-11-03 CN disclosed
EP-2229356-A1 1,2-DISUBSTITUTED-4-BENZYLAMINO-PYRROLIDINE DERIVATIVES AS CETP INHIBITORS USEFUL FOR THE TREATMENT OF DISEASES SUCH AS HYPERLI PIDEMIA OR ARTERIOSCLEROSIS Novartis AG (CH) 2010-09-22 EP disclosed
WO-2009071509-A1 1,2-DISUBSTITUTED-4-BENZYLAMINO-PYRROLIDINE DERIVATIVES AS CETP INHIBITORS USEFUL FOR THE TREATMENT OF DISEASES SUCH AS HYPERLI PIDEMIA OR ARTERIOSCLEROSIS NOVARTIS AG (CH) 2009-06-11 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-20180194783-A1 BETA-LACTAMASE INHIBITORS MGAM, GAA, LCT MGAM 1/4885GAA 2/4885SI 32/4885
US-20250236632-A1 BETA-LACTAMASE INHIBITORS MGAM, GAA, LCT MGAM 1/4885GAA 2/4885SI 32/4885
US-20190225628-A1 BETA-LACTAMASE INHIBITORS MGAM, GAA, LCT MGAM 1/4885GAA 2/4885SI 32/4885
US-10669290-B2 Beta-lactamase inhibitors MGAM, GAA, LCT MGAM 1/4885GAA 2/4885SI 32/4885
US-20190002414-A1 NK1 RECEPTOR ANTAGONIST TACR1, TACR2, GRPR MGAM 4808/4885GAA 4798/4885SI 2761/4885
US-20140171390-A1 BETA-LACTAMASE INHIBITORS MGAM, GAA, LCT MGAM 1/4885GAA 2/4885SI 32/4885
US-20100311750-A1 ORGANIC COMPOUNDS CETP, NPC1, CES1 MGAM 3551/4885GAA 641/4885SI 3642/4885
US-10399949-B2 NK1 receptor antagonist TACR1, TACR2, GRPR MGAM 4808/4885GAA 4798/4885SI 2761/4885

“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.