Physostigmine

Physostigmine

SCHEMBL60805

Br.CNC(=O)Oc1ccc2c(c1)[C@]1(C)CCN(C)[C@@H]1N2C

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHE

The experimentally established mechanism targets of Physostigmine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 14/20 0.98
BCHE P06276 11/20 0.98
KDM4E B2RXH2 7/20 0.98
ALDH1A1 P00352 5/20 0.98
SMN1; SMN2 Q16637 3/20 0.98
CYP2D6 P10635 2/20 0.98
HIF1A Q16665 2/20 0.98
MEN1 O00255 1/20 0.98
CYP1A2 P05177 1/20 0.98
KMT2A Q03164 1/20 0.98
LMNA P02545 1/20 0.98
PTGS1 P23219 1/20 0.98
OPRM1 P35372 1/20 0.98
OPRK1 P41145 1/20 0.98
BLM P54132 1/20 0.98
HRH3 Q9Y5N1 1/20 0.98
HSD17B10 Q99714 2/20 0.90
HPGD P15428 2/20 0.77
NPC1 O15118 1/20 0.74
MAPT P10636 1/20 0.74

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
Physostigmine SCHEMBL7587896 1.00 ACHE (0.98) ACHEBCHEKDM4EALDH1A1SMN1; SMN2
Physostigmine SCHEMBL29482277 0.99 ACHE (1.00) ACHEBCHEKDM4EALDH1A1SMN1; SMN2
Physostigmine SCHEMBL4104619 0.99 ACHE (1.00) ACHEBCHEKDM4EALDH1A1SMN1; SMN2
Physostigmine SCHEMBL24044 0.99 ACHE (1.00) ACHEBCHEKDM4EALDH1A1SMN1; SMN2
Physostigmine SCHEMBL8800695 0.99 ACHE (1.00) ACHEBCHEKDM4EALDH1A1SMN1; SMN2
Physostigmine SCHEMBL9988368 0.99 ACHE (1.00) ACHEBCHEKDM4EALDH1A1SMN1; SMN2
Physostigmine SCHEMBL24045 0.99 ACHE (1.00) ACHEBCHEKDM4EALDH1A1SMN1; SMN2
Physostigmine SCHEMBL13930339 0.99 ACHE (1.00) ACHEBCHEKDM4EALDH1A1SMN1; SMN2
(+)-Physostigmine SCHEMBL15677750 0.99 ACHE (1.00) ACHEBCHEKDM4EALDH1A1SMN1; SMN2
Physostigmine SCHEMBL7581684 0.98 ACHE (0.98) ACHEBCHEKDM4EALDH1A1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1061952-A2 COMBINATION OF A GABA-A ALPHA 5 INVERSE AGONIST AND AN ACETYLCHOLINESTERASE INHIBITOR MERCK SHARP & DOHME LTD. (GB) 2000-12-27 EP claimed
WO-1999047131-A2 COMBINATION OF A GABA-A ALPHA 5 INVERSE AGONIST AND AN ACETYLCHOLINESTERASE INHIBITOR MERCK SHARP & DOHME LIMITED (GB) 1999-09-23 WO claimed
EP-4289838-A2 ARYLMETHOXY ISOINDOLINE DERIVATIVES AND COMPOSITIONS COMPRISING AND METHODS OF USING THE SAME Celgene Corporation (US) 2023-12-13 EP disclosed
US-11820720-B2 3-(5-substituted-4-oxoquinazolin-3(4H)-yl)-3-deuteropiperidine-2,6-dione derivatives and compositions comprising and methods of using the same SALARIUS PHARMACEUTICALS, INC. (US) 2023-11-21 US disclosed
US-11773080-B2 Deuterium-enriched isoindolinonyl-azepanediones and related compounds and methods of treating medical disorders using same SALARIUS PHARMACEUTICALS, INC. (US) 2023-10-03 US disclosed
US-RE49647-E1 Formulations of (S)-3-(4-((4-(morpholinomethyl)benzyl)oxy)-1-oxoisoindolin-2-yl)piperidine-2,6-dione CELGENE CORPORATION (US) 2023-09-12 US disclosed
US-20230277539-A1 3-(SUBSTITUTED-4-OXOQUINAZOLIN-3(4H)-YL)-3-DEUTERO-PIPERIDINE-2,6-DIONE DERIVATIVES AND COMPOSITIONS COMPRISING AND METHODS OF USING THE SAME DEUTERX LLC (US) 2023-09-07 US disclosed
EP-3599236-B1 ARYLMETHOXY ISOINDOLINE DERIVATIVES AND COMPOSITIONS COMPRISING AND METHODS OF USING THE SAME CELGENE CORP (US) 2023-08-23 EP disclosed
US-20230242504-A1 DEUTERIUM-ENRICHED PIPERIDINONYL-OXOISOINDOLINYL ACETAMIDES AND METHODS OF TREATING MEDICAL DISORDERS USING SAME DEUTERX LLC (US) 2023-08-03 US disclosed
EP-3660020-B1 PROCESS FOR THE SYNTHESIS OF MTOR KINASE INHIBITORS SIGNAL PHARM LLC (US) 2023-07-05 EP disclosed
US-20230119470-A1 PYRAZINO[2,3-b]PYRAZINE mTOR KINASE INHIBITORS FOR ONCOLOGY INDICATIONS AND DISEASES ASSOCIATED WITH THE mTOR/PI3K/AKT PATHWAY SIGNAL PHARM LLC (US) 2023-04-20 US disclosed
WO-2005065455-A1 IMMUNOMODULATORY COMPOUNDS FOR THE TREATMENT OF CENTRAL NERVOUS SYSTEM DISORDERS CELGENE CORPORATION (US) 2005-07-21 WO disclosed
WO-2005065372-A2 METHODS AND COMPOSITIONS USING THALIDOMIDE FOR THE TREATMENT AND MANAGEMENT OF CENTRAL NERVOUS SYSTEM DISORDERS OR DISEASES CELGENE CORPORATION (US) 2005-07-21 WO disclosed
US-20050143344-A1 Methods and compositions using immunomodulatory compounds for the treatment and management of central nervous system disorders or diseases CELGENE CORPORATION 2005-06-30 US disclosed
EP-1543157-A2 METHODS FOR IDENTIFYING SMALL MOLEDULES THAT MODULATE PREMATURE TRANSLATION TERMINATION AND NONSENSE MEDIATED mRNA DECAY PTC Therapeutics, Inc. (US) 2005-06-22 EP disclosed
WO-2004080393-A2 SELECTIVE CYTOKINE INHIBITORY DRUGS FOR TREATING DISORDERS OF THE CENTRAL NERVOUS SYSTEM CELGENE CORPORATION (US) 2004-09-23 WO disclosed
US-20040175382-A1 Methods of using and compositions comprising selective cytokine inhibitory drugs for the treatment and management of disorders of the central nervous system CELGENE CORPORATION 2004-09-09 US disclosed
WO-2004010106-A2 METHODS FOR IDENTIFYING SMALL MOLEDULES THAT MODULATE PREMATURE TRANSLATION TERMINATION AND NONSENSE MEDIATED mRNA DECAY PTC THERAPEUTICS, INC. (US) 2004-01-29 WO disclosed
WO-2004001010-A2 METHODS FOR IDENTIFYING SMALL MOLECULES THAT MODULATE PREMATURE TRANSLATION TERMINATION AND NONSENSE MEDIATED mRNA DECAY PTC THERAPEUTICS, INC. (US) 2003-12-31 WO disclosed
WO-2002099982-A2 METHODS FOR IMPROVING SIGNAL DETECTION FROM AN ARRAY ILLUMINA, INC. (US) 2002-12-12 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 (7 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-11820720-B2 3-(5-substituted-4-oxoquinazolin-3(4H)-yl)-3-deuteropiperidine-2,6-dione derivatives and compositions comprising and methods of using the same IL5, IL15, CXCR5 ACHE 4820/4885BCHE 4732/4885KDM4E 705/4885
US-20230242504-A1 DEUTERIUM-ENRICHED PIPERIDINONYL-OXOISOINDOLINYL ACETAMIDES AND METHODS OF TREATING MEDICAL DISORDERS USING SAME EGLN3, HPGDS, EGLN2 ACHE 3399/4885BCHE 3152/4885KDM4E 1112/4885
US-20230119470-A1 PYRAZINO[2,3-b]PYRAZINE mTOR KINASE INHIBITORS FOR ONCOLOGY INDICATIONS AND DISEASES ASSOCIATED WITH THE mTOR/PI3K/AKT PATHWAY MTOR, RICTOR, RPTOR ACHE 3218/4885BCHE 2930/4885KDM4E 2119/4885
US-11773080-B2 Deuterium-enriched isoindolinonyl-azepanediones and related compounds and methods of treating medical disorders using same HPGDS, HPGD, AQP3 ACHE 3754/4885BCHE 2983/4885KDM4E 732/4885
US-20050143344-A1 Methods and compositions using immunomodulatory compounds for the treatment and management of central nervous system disorders or diseases SMN1; SMN2, GBA1, AQP4 ACHE 18/4885BCHE 32/4885KDM4E 3601/4885
US-20230277539-A1 3-(SUBSTITUTED-4-OXOQUINAZOLIN-3(4H)-YL)-3-DEUTERO-PIPERIDINE-2,6-DIONE DERIVATIVES AND COMPOSITIONS COMPRISING AND METHODS OF USING THE SAME AQP3, AQP4, AQP1 ACHE 3625/4885BCHE 4171/4885KDM4E 1210/4885
US-20040175382-A1 Methods of using and compositions comprising selective cytokine inhibitory drugs for the treatment and management of disorders of the central nervous system IL2, IL6, BDNF ACHE 53/4885BCHE 106/4885KDM4E 4739/4885

“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.