Sparteine

Sparteine

SCHEMBL8913122

C1CCN2CC3CC(CN4CCCCC34)C2C1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
▸ CYP2D6 P10635 4/20 1.00
▸ MEN1 O00255 3/20 1.00
▸ KMT2A Q03164 3/20 1.00
▸ LMNA P02545 1/20 1.00
▸ KDM4E B2RXH2 2/20 0.46
▸ ALDH1A1 P00352 2/20 0.46
▸ CYP2C19 P33261 1/20 0.46
▸ HSD17B10 Q99714 1/20 0.46
▸ TDP1 Q9NUW8 1/20 0.39
▸ SLC18A3 Q16572 2/20 0.37
▸ PKM P14618 1/20 0.33

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
Sparteine SCHEMBL29352895 1.00 CYP2D6 (1.00) CYP2D6MEN1KMT2ALMNAKDM4E
Sparteine SCHEMBL14029290 1.00 CYP2D6 (1.00) CYP2D6MEN1KMT2ALMNAKDM4E
Sparteine SCHEMBL13646782 1.00 CYP2D6 (1.00) CYP2D6MEN1KMT2ALMNAKDM4E
Sparteine SCHEMBL1753344 1.00 CYP2D6 (1.00) CYP2D6MEN1KMT2ALMNAKDM4E
Sparteine SCHEMBL12573662 1.00 CYP2D6 (1.00) CYP2D6MEN1KMT2ALMNAKDM4E
Sparteine SCHEMBL18468288 1.00 CYP2D6 (1.00) CYP2D6MEN1KMT2ALMNAKDM4E
Sparteine SCHEMBL14331495 1.00 CYP2D6 (1.00) CYP2D6MEN1KMT2ALMNAKDM4E
Sparteine SCHEMBL13531828 1.00 CYP2D6 (1.00) CYP2D6MEN1KMT2ALMNAKDM4E
Sparteine SCHEMBL12301225 1.00 CYP2D6 (1.00) CYP2D6MEN1KMT2ALMNAKDM4E
Sparteine SCHEMBL22619501 1.00 CYP2D6 (1.00) CYP2D6MEN1KMT2ALMNAKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5100647-A Method and formulations for the therapy of cystic fibrosis, Bartter's syndrome and secretory diarrheas, and for diuretic treatment THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 1992-03-31 — — US claimed
US-20230212351-A1 METHOD FOR PRODUCING BLOCK COPOLYMER COMPRISING CYCLIC ESTER AND EPOXY MONOMERS ARRANGED IN CONTROLLABLE SEQUENCE SOUTH CHINA UNIVERSITY OF TECHNOLOGY (CN) 2023-07-06 — — US disclosed
WO-2021043315-A1 METHOD FOR PRODUCING BLOCK COPOLYMER COMPRISING CYCLIC ESTER AND EPOXY MONOMERS ARRANGED IN CONTROLLABLE SEQUENCE 华南理工大学 2021-03-11 — — WO disclosed
EP-2984117-B1 VITAMIN FUNCTIONALIZED GEL-FORMING BLOCK COPOLYMERS FOR BIOMEDICAL APPLICATIONS IBM (US) 2018-04-25 — — EP disclosed
EP-3004105-B1 PROCESS FOR CONVERTING LUPANINE INTO SPARTEINE MAULIDE NUNO (AT) 2017-09-06 — — EP disclosed
US-9388182-B2 Process for converting lupanine into sparteine STUDIENGESELLSCHAFT KOHLE MBH (DE) 2016-07-12 — — US disclosed
US-9388182-B2 Process for converting lupanine into sparteine STUDIENGESELLSCHAFT KOHLE MBH (DE) 2016-07-12 — — US disclosed
US-20160096840-A1 PROCESS FOR CONVERTING LUPANINE INTO SPARTEINE STUDIENGESELLSCHAFT KOHLE MBH (DE) 2016-04-07 — — US disclosed
US-20160096840-A1 PROCESS FOR CONVERTING LUPANINE INTO SPARTEINE STUDIENGESELLSCHAFT KOHLE MBH (DE) 2016-04-07 — — US disclosed
WO-2014191261-A1 PROCESS FOR CONVERTING LUPANINE INTO SPARTEINE STUDIENGESELLSCHAFT KOHLE MBH (DE) 2014-12-04 — — WO disclosed
US-8216487-B2 Copolymer of propylene or ethylene oxide and of an oxirane bearing an ionic group BATSCAP (FR) 2012-07-10 — — US disclosed
US-8216487-B2 Copolymer of propylene or ethylene oxide and of an oxirane bearing an ionic group BATSCAP (FR) 2012-07-10 — — US disclosed
US-20110319657-A1 Process for the Preparation of Formic Acid BASF SE (DE) 2011-12-29 — — US disclosed
US-20110054176-A1 QUINOLINE-OXAZOLINE COMPOUNDS AND THEIR USE IN OXIDATION SYNTHESIS NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2011-03-03 — — US disclosed
US-20090176161-A1 COPOLYMER OF PROPYLENE OR ETHYLENE OXIDE AND OF AN OXIRANE BEARING AN IONIC GROUP BLUE SOLUTIONS (FR) 2009-07-09 — — US disclosed
US-20090176161-A1 COPOLYMER OF PROPYLENE OR ETHYLENE OXIDE AND OF AN OXIRANE BEARING AN IONIC GROUP BLUE SOLUTIONS (FR) 2009-07-09 — — US disclosed
US-7402670-B2 Synthesis by chiral diamine-mediated asymmetric alkylation JANSSEN PHARMACEUTICA, N.V. (BE) 2008-07-22 — — US disclosed
US-5621007-A Method for regulation of transmembrane chloride conductance BRISTOL-MYERS SQUIBB COMPANY (US) 1997-04-15 — — US disclosed
US-5100647-A Method and formulations for the therapy of cystic fibrosis, Bartter's syndrome and secretory diarrheas, and for diuretic treatment THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 1992-03-31 — — US disclosed
US-5100647-A Method and formulations for the therapy of cystic fibrosis, Bartter's syndrome and secretory diarrheas, and for diuretic treatment THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 1992-03-31 — — US 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 (2 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-20110054176-A1 QUINOLINE-OXAZOLINE COMPOUNDS AND THEIR USE IN OXIDATION SYNTHESIS XDH, OXA1L, AOX1 CYP2D6 139/4885MEN1 1471/4885KMT2A 1323/4885
US-20160096840-A1 PROCESS FOR CONVERTING LUPANINE INTO SPARTEINE SPR, GCLC, GSTP1 CYP2D6 27/4885MEN1 3941/4885KMT2A 4195/4885

“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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