SCHEMBL29376236

SCHEMBL29376236

COc1ccc(C[C@@H]2c3cc(OC)c(O)cc3CCN2C)cc1O

nearest known ligand 0.91

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
▸ DRD2 P14416 2/20 0.91
▸ DRD1 P21728 1/20 0.91
▸ LMNA P02545 2/20 0.76
▸ KDM4E B2RXH2 2/20 0.76
▸ ALDH1A1 P00352 2/20 0.76
▸ HSD17B10 Q99714 2/20 0.76
▸ MAPK1 P28482 1/20 0.76
▸ CYP2D6 P10635 1/20 0.76
▸ BCHE P06276 1/20 0.74
▸ ACHE P22303 1/20 0.74
▸ KCNH2 Q12809 2/20 0.74
▸ ALOX15 P16050 1/20 0.71
▸ DRD4 P21917 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
Laudanidine SCHEMBL18187574 0.95 DRD2 (0.95) DRD2DRD1LMNAKDM4EALDH1A1
Laudanidine SCHEMBL15696580 0.95 DRD2 (0.91) DRD2DRD1LMNAKDM4EALDH1A1
(S)-Reticuline SCHEMBL29923953 0.95 DRD2 (1.00) DRD2DRD1LMNAKDM4EALDH1A1
Laudanidine SCHEMBL679495 0.95 DRD2 (0.91) DRD2DRD1LMNAKDM4EALDH1A1
(R)-Reticuline SCHEMBL29364903 0.95 DRD2 (1.00) DRD2DRD1LMNAKDM4EALDH1A1
(S)-Reticuline SCHEMBL147597 0.95 DRD2 (1.00) DRD2DRD1LMNAKDM4EALDH1A1
(S)-Reticuline SCHEMBL147596 0.95 DRD2 (1.00) DRD2DRD1LMNAKDM4EALDH1A1
Laudanidine SCHEMBL30589210 0.95 DRD2 (0.91) DRD2DRD1LMNAKDM4EALDH1A1
(R)-Reticuline SCHEMBL29373552 0.95 DRD2 (1.00) DRD2DRD1LMNAKDM4EALDH1A1
(R)-Reticuline SCHEMBL9587509 0.95 DRD2 (1.00) DRD2DRD1LMNAKDM4EALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240299481-A1 STEPHANIA CEPHARANTHA-DERIVED ALKALOID-CONTAINING PREPARATION SAWAI PHARMACEUTICAL CO., LTD. (JP) 2024-09-12 — — US claimed
US-11542481-B2 Morphinan N-demethylase isolated from the methylobacterium thebainfresser and methods of use thereof DONALD DANFORTH PLANT SCIENCE CENTER (US) 2023-01-03 — — US claimed
US-20260103736-A1 Methods Of Improving Production Of Morphinan Alkaloids And Derivatives ANTHEIA INC (US) 2026-04-16 — — US disclosed
US-12497638-B2 Methods of producing epimerases and benzylisoquinoline alkaloids THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2025-12-16 — — US disclosed
EP-4594342-A2 METHODS OF IMPROVING PRODUCTION OF MORPHINAN ALKALOIDS AND DERIVATIVES Antheia, Inc. (US) 2025-08-06 — — EP disclosed
US-20250137021-A1 METHODS OF PRODUCING NOR-OPIOID AND NAL-OPIOID BENZYLISOQUINOLINE ALKALOIDS HERCULES CAPITAL, INC., AS AGENT 2025-05-01 — — US disclosed
US-12180525-B2 Methods of producing nor-opioid and nal-opioid benzylisoquinoline alkaloids ANTHEIA, INC. (US) 2024-12-31 — — US disclosed
EP-4434521-A1 STEPHANIA CEPHALANTHA-DERIVED ALKALOID-CONTAINING PREPARATION Japan As Represented By Director-General Of National Institute Of Infectious Diseases (JP) 2024-09-25 — — EP disclosed
US-20240299481-A1 STEPHANIA CEPHARANTHA-DERIVED ALKALOID-CONTAINING PREPARATION SAWAI PHARMACEUTICAL CO., LTD. (JP) 2024-09-12 — — US disclosed
CN-118555958-A Preparation containing alkaloid from Anoectochilus formosanus 国立感染症研究所所长代表的日本国 2024-08-27 — — CN disclosed
US-20240218408-A1 Methods of Producing Epimerases and Benzylisoquinoline Alkaloids HERCULES CAPITAL, INC., AS AGENT 2024-07-04 — — US disclosed
WO-2023089862-A1 STEPHANIA CEPHALANTHA-DERIVED ALKALOID-CONTAINING PREPARATION 国立感染症研究所長が代表する日本国 2023-05-25 — — WO disclosed
EP-3294865-B1 METHODS OF PRODUCING EPIMERASES AND BENZYLISOQUINOLINE ALKALOIDS UNIV LELAND STANFORD JUNIOR (US) 2023-04-12 — — EP disclosed
US-20230104286-A1 METHODS OF PRODUCING NOR-OPIOID AND NAL-OPIOID BENZYLISOQUINOLINE ALKALOIDS HERCULES CAPITAL, INC., AS AGENT 2023-04-06 — — US disclosed
US-11542481-B2 Morphinan N-demethylase isolated from the methylobacterium thebainfresser and methods of use thereof DONALD DANFORTH PLANT SCIENCE CENTER (US) 2023-01-03 — — US disclosed
US-11427827-B2 Engineered benzylisoquinoline alkaloid epimerases and methods of producing benzylisoquinoline alkaloids ANTHEIA, INC. (US) 2022-08-30 — — US disclosed
US-11396668-B2 Methods of producing nor-opioid and nal-opioid benzylisoquinoline alkaloids ANTHEIA, INC. (US) 2022-07-26 — — US disclosed
WO-2022109194-A1 METHODS OF IMPROVING PRODUCTION OF MORPHINAN ALKALOIDS AND DERIVATIVES ANTHEIA, INC. (US) 2022-05-27 — — WO disclosed
US-20220162656-A1 METHODS OF IMPROVING PRODUCTION OF MORPHINAN ALKALOIDS AND DERIVATIVES HERCULES CAPITAL, INC., AS AGENT 2022-05-26 — — US disclosed
EP-3947633-A1 METHODS OF IMPROVING PRODUCTION OF MORPHINAN ALKALOIDS AND DERIVATIVES Antheia, Inc. (US) 2022-02-09 — — 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 (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-20260103736-A1 Methods Of Improving Production Of Morphinan Alkaloids And Derivatives OPRK1, OPRM1, OPRD1 DRD2 618/4885DRD1 532/4885LMNA 3778/4885
US-20240299481-A1 STEPHANIA CEPHARANTHA-DERIVED ALKALOID-CONTAINING PREPARATION SARS1, BCDIN3D, CCL5 DRD2 2333/4885DRD1 2338/4885LMNA 3385/4885

“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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