SCHEMBL737244

SCHEMBL737244

O=C1CN[C@@H](c2ccccc2)CO1

nearest known ligand 0.46

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
PRCP P42785 1/20 0.46
CYP19A1 P11511 3/20 0.38
TSHR P16473 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.37
AR P10275 1/20 0.35
MEN1 O00255 2/20 0.34
KMT2A Q03164 2/20 0.34
CA2 P00918 1/20 0.34
LMNA P02545 1/20 0.34

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
SCHEMBL739240 1.00 PRCP (0.46) PRCPCYP19A1TSHRSMN1; SMN2AR
SCHEMBL737577 1.00 PRCP (0.46) PRCPCYP19A1TSHRSMN1; SMN2AR
Hydrochloric Acid SCHEMBL14472340 0.98 PRCP (0.44) PRCPCYP19A1TSHRSMN1; SMN2AR
Hydrochloric Acid SCHEMBL736275 0.98 PRCP (0.44) PRCPCYP19A1TSHRSMN1; SMN2AR
SCHEMBL8266504 0.78 PRCP (0.46) PRCPCYP19A1TSHRARMEN1
Hydrochloric Acid SCHEMBL28764877 0.78 HSD11B1 (0.34) PRCPMEN1KMT2ALMNA
SCHEMBL20915054 0.75 PRCP (0.56) PRCPCYP19A1TSHRMEN1KMT2A
SCHEMBL445133 0.73 SMN1; SMN2 (0.42) CYP19A1TSHRSMN1; SMN2ARMEN1
SCHEMBL4562 0.73 SMN1; SMN2 (0.42) CYP19A1TSHRSMN1; SMN2ARMEN1
SCHEMBL16106147 0.73 SMN1; SMN2 (0.42) CYP19A1TSHRSMN1; SMN2ARMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210171507-A1 SYNTHESIS OF UDP-GLUCOSE: N-ACYLSPHINGOSINE GLUCOSYLTRANSFERASE INHIBITORS GENZYME CORPORATION 2021-06-10 US claimed
US-20190322649-A1 SYNTHESIS OF UDP-GLUCOSE: N-ACYLSPHINGOSINE GLUCOSYLTRANSFERASE INHIBITORS GENZYME CORPORATION 2019-10-24 US claimed
US-20170334888-A1 SYNTHESIS OF UDP-GLUCOSE: N-ACYLSPHINGOSINE GLUCOSYLTRANSFERASE INHIBITORS GENZYME CORPORATION 2017-11-23 US claimed
WO-2026087442-A1 AMINO-IMIDAZOLE ANTIBACTERIAL COMPOUNDS F. HOFFMANN-LA ROCHE AG (CH) 2026-04-30 WO disclosed
US-20260062420-A1 NOVEL DPP1 INHIBITORS AND USES THEREOF INSMED INC (US) 2026-03-05 US disclosed
US-12398114-B2 Process for the preparation of ELIGLUSTAT and its intermediate PIRAMAL PHARMA LIMITED (IN) 2025-08-26 US disclosed
EP-4561565-A2 NOVEL DPP1 INHIBITORS AND USES THEREOF Insmed Incorporated (US) 2025-06-04 EP disclosed
EP-4142878-B1 PYRIDINE INHIBITORS OF GLUCOSYLCERAMIDE SYNTHASE AND THERAPEUTIC METHODS USING THE SAME UNIV MICHIGAN REGENTS (US) 2024-06-26 EP disclosed
EP-4142878-B1 PYRIDINE INHIBITORS OF GLUCOSYLCERAMIDE SYNTHASE AND THERAPEUTIC METHODS USING THE SAME UNIV MICHIGAN REGENTS (US) 2024-06-26 EP disclosed
WO-2024026433-A2 NOVEL DPP1 INHIBITORS AND USES THEREOF INSMED INCORPORATED (US) 2024-02-01 WO disclosed
US-11697644-B2 Process for synthesis of eliglustat and intermediate compounds thereof ZHEJIANG AUSUN PHARMACEUTICAL CO., LTD. (CN) 2023-07-11 US disclosed
US-7196205-B2 Synthesis of amino ceramide-like compounds; for treating Tay-Sachs, Gaucher's or Fabry's disease; amenable to large scale preparations THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2007-03-27 US disclosed
US-7196205-B2 Synthesis of amino ceramide-like compounds; for treating Tay-Sachs, Gaucher's or Fabry's disease; amenable to large scale preparations THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2007-03-27 US disclosed
US-20050222244-A1 Synthesis of UDP-glucose: N-acylsphingosine glucosyltransferase inhibitors GENZYME CORPORATION (US) 2005-10-06 US disclosed
US-6855830-B2 Synthesis of UDP-glucose: N-acylsphingosine glucosyltransferase inhibitors GENZYME CORPORATION (US) 2005-02-15 US disclosed
US-20050009872-A1 Synthesis of UDP-glucose: N-acylsphingosine glucosyltransferase inhibitors GENZYME CORPORATION (US) 2005-01-13 US disclosed
EP-1409467-A1 SYNTHESIS OF UDP-GLUCOSE: N-ACYLSPHINGOSINE GLUCOSYLTRANSFERASE INHIBITORS GENZYME CORPORATION (US) 2004-04-21 EP disclosed
US-20030050299-A1 An intermediates for enantiomeric synthesis cermamide-like inhibitors; producing antilipemic agents GENZYME CORPORATION 2003-03-13 US disclosed
US-20030050299-A1 An intermediates for enantiomeric synthesis cermamide-like inhibitors; producing antilipemic agents GENZYME CORPORATION 2003-03-13 US disclosed
WO-2003008399-A1 SYNTHESIS OF UDP-GLUCOSE: N-ACYLSPHINGOSINE GLUCOSYLTRANSFERASE INHIBITORS GENZYME CORPORATION (US) 2003-01-30 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-20050222244-A1 Synthesis of UDP-glucose: N-acylsphingosine glucosyltransferase inhibitors UGCG, UGGT1, DPAGT1 PRCP 1736/4885CYP19A1 3114/4885TSHR 4491/4885
US-20210171507-A1 SYNTHESIS OF UDP-GLUCOSE: N-ACYLSPHINGOSINE GLUCOSYLTRANSFERASE INHIBITORS UGCG, UGGT1, DPAGT1 PRCP 1736/4885CYP19A1 3114/4885TSHR 4491/4885
US-20170334888-A1 SYNTHESIS OF UDP-GLUCOSE: N-ACYLSPHINGOSINE GLUCOSYLTRANSFERASE INHIBITORS UGCG, UGGT1, DPAGT1 PRCP 1736/4885CYP19A1 3114/4885TSHR 4491/4885
US-11697644-B2 Process for synthesis of eliglustat and intermediate compounds thereof EPOR, FGFR1, ABL1 PRCP 1424/4885CYP19A1 1003/4885TSHR 2762/4885
US-20190322649-A1 SYNTHESIS OF UDP-GLUCOSE: N-ACYLSPHINGOSINE GLUCOSYLTRANSFERASE INHIBITORS UGCG, UGGT1, DPAGT1 PRCP 1736/4885CYP19A1 3114/4885TSHR 4491/4885
US-20050009872-A1 Synthesis of UDP-glucose: N-acylsphingosine glucosyltransferase inhibitors UGCG, UGGT1, DPAGT1 PRCP 1736/4885CYP19A1 3114/4885TSHR 4491/4885
US-12398114-B2 Process for the preparation of ELIGLUSTAT and its intermediate OGFR, OXGR1, OGFRL1 PRCP 1064/4885CYP19A1 463/4885TSHR 381/4885
US-20260062420-A1 NOVEL DPP1 INHIBITORS AND USES THEREOF DPP4, DPP3, DPP7 PRCP 309/4885CYP19A1 3385/4885TSHR 1077/4885
US-20030050299-A1 An intermediates for enantiomeric synthesis cermamide-like inhibitors; producing antilipemic agents UGCG, UGGT1, LCLAT1 PRCP 826/4885CYP19A1 1621/4885TSHR 3968/4885

“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.