(-)-Higenamine

(-)-Higenamine

SCHEMBL5898911

Oc1ccc(C[C@@H]2NCCc3cc(O)c(O)cc32)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
DRD2 P14416 2/20 1.00
DRD4 P21917 2/20 1.00
KDM1A O60341 1/20 1.00
TBXA2R P21731 6/20 0.80
ADRB2 P07550 5/20 0.79
MEN1 O00255 1/20 0.79
ABL1 P00519 1/20 0.79
ALPL P05186 1/20 0.79
GAA P10253 1/20 0.79
KMT2A Q03164 1/20 0.79
RIN1 Q13671 1/20 0.79
KDM4E B2RXH2 1/20 0.74
MAPT P10636 1/20 0.74
PKM P14618 1/20 0.74
ADRB1 P08588 1/20 0.70
BCHE P06276 1/20 0.70

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
(+)-Higenamine SCHEMBL5898913 1.00 DRD2 (1.00) DRD2DRD4KDM1ATBXA2RADRB2
(+)-Higenamine SCHEMBL30464469 1.00 DRD2 (1.00) DRD2DRD4KDM1ATBXA2RADRB2
(-)-Higenamine SCHEMBL29365055 1.00 DRD2 (1.00) DRD2DRD4KDM1ATBXA2RADRB2
Higenamine SCHEMBL30105922 1.00 DRD2 (1.00) DRD2DRD4KDM1ATBXA2RADRB2
Higenamine SCHEMBL636788 1.00 DRD2 (1.00) DRD2DRD4KDM1ATBXA2RADRB2
(-)-Higenamine SCHEMBL5898916 0.99 DRD2 (0.97) DRD2DRD4KDM1ATBXA2RADRB2
(-)-Higenamine SCHEMBL29374757 0.99 DRD2 (0.97) DRD2DRD4KDM1ATBXA2RADRB2
(+)-Higenamine SCHEMBL5898932 0.99 DRD2 (0.97) DRD2DRD4KDM1ATBXA2RADRB2
Higenamine SCHEMBL28478764 0.99 DRD2 (0.97) DRD2DRD4KDM1ATBXA2RADRB2
Higenamine SCHEMBL29623874 0.99 DRD2 (0.97) DRD2DRD4KDM1ATBXA2RADRB2

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 16 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20060058346-A1 Novel enantiomers of etrahydroisoquinoline derivatives and theirpharmaceutically acceptable salts, their preparations and pharmaceutical compositions YUN-CHOI HYE-SOOK 2006-03-16 US claimed
EP-1507764-A4 NOVEL ENANTIOMERS OF TETRAHYDROISOQUINOLINE DERIVATIVES AND THEIR PHARMACEUTICALLY ACCEPTABLE SALTS, THEIR PREPARATIONS AND PHARMACEUTICAL COMPOSITIONS YUN-CHOI HYE-SOOK (KR) 2005-06-22 EP claimed
CN-1630640-A Novel enantiomer of tetra hydrogen isoquinoline derivative and officinal salt, preparation and pharmaceutical composition thereof HOI-SU YOON CHOI (KR) 2005-06-22 CN claimed
EP-1507764-A1 NOVEL ENANTIOMERS OF TETRAHYDROISOQUINOLINE DERIVATIVES AND THEIR PHARMACEUTICALLY ACCEPTABLE SALTS, THEIR PREPARATIONS AND PHARMACEUTICAL COMPOSITIONS Yun-Choi, Hye-Sook (KR) 2005-02-23 EP claimed
WO-2003095426-A1 NOVEL ENANTIOMERS OF TETRAHYDROISOQUINOLINE DERIVATIVES AND THEIR PHARMACEUTICALLY ACCEPTABLE SALTS, THEIR PREPARATIONS AND PHARMACEUTICAL COMPOSITIONS YUN-CHOI HYE-SOOK (KR) 2003-11-20 WO claimed
US-10738335-B2 Methods of producing nor-opioid and nal-opioid benzylisoquinoline alkaloids ANTHEIA, INC. (US) 2020-08-11 US disclosed
US-10662453-B2 Compositions and methods for making (S)-norcoclaurine and (S)-norlaudanosoline, and synthesis intermediates thereof Willow Biosciences Inc. (CA) 2020-05-26 US disclosed
US-20190144900-A1 METHODS OF PRODUCING NOR-OPIOID AND NAL-OPIOID BENZYLISOQUINOLINE ALKALOIDS HERCULES CAPITAL, INC., AS AGENT 2019-05-16 US disclosed
CN-103626703-B The preparation method of chirality demethyl coclaurine and derivative thereof ZHUHAI RUNDU PHARMACEUTICAL CO., LTD. (CN) 2015-11-11 CN disclosed
CN-103626703-A Preparation method of chiral higenamine and derivatives of chiral higenamine ZHUHAI RUNDU PHARMACEUTICAL CO LTD 2014-03-12 CN disclosed
CN-100348583-C Novel enantiomer of tetra hydrogen isoquinoline derivative and officinal salt, preparation and pharmaceutical composition thereof YOON CHOI HOI SU (KR) 2007-11-14 CN disclosed
US-20060058346-A1 Novel enantiomers of etrahydroisoquinoline derivatives and theirpharmaceutically acceptable salts, their preparations and pharmaceutical compositions YUN-CHOI HYE-SOOK 2006-03-16 US disclosed
EP-1507764-A4 NOVEL ENANTIOMERS OF TETRAHYDROISOQUINOLINE DERIVATIVES AND THEIR PHARMACEUTICALLY ACCEPTABLE SALTS, THEIR PREPARATIONS AND PHARMACEUTICAL COMPOSITIONS YUN-CHOI HYE-SOOK (KR) 2005-06-22 EP disclosed
CN-1630640-A Novel enantiomer of tetra hydrogen isoquinoline derivative and officinal salt, preparation and pharmaceutical composition thereof HOI-SU YOON CHOI (KR) 2005-06-22 CN disclosed
EP-1507764-A1 NOVEL ENANTIOMERS OF TETRAHYDROISOQUINOLINE DERIVATIVES AND THEIR PHARMACEUTICALLY ACCEPTABLE SALTS, THEIR PREPARATIONS AND PHARMACEUTICAL COMPOSITIONS Yun-Choi, Hye-Sook (KR) 2005-02-23 EP disclosed
WO-2003095426-A1 NOVEL ENANTIOMERS OF TETRAHYDROISOQUINOLINE DERIVATIVES AND THEIR PHARMACEUTICALLY ACCEPTABLE SALTS, THEIR PREPARATIONS AND PHARMACEUTICAL COMPOSITIONS YUN-CHOI HYE-SOOK (KR) 2003-11-20 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 (1 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-20060058346-A1 Novel enantiomers of etrahydroisoquinoline derivatives and theirpharmaceutically acceptable salts, their preparations and pharmaceutical compositions TBXA2R, NOS2, TBXAS1 DRD2 641/4885DRD4 1187/4885KDM1A 3491/4885

“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.