Atropine Oxide

Atropine Oxide

SCHEMBL162929

C[N+]1([O-])[C@@H]2CC[C@H]1C[C@@H](OC(=O)C(CO)c1ccccc1)C2

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP2C19 P33261 1/20 1.00
CHRM2 P08172 6/20 0.82
BLM P54132 4/20 0.80
PABPC1 P11940 1/20 0.80
SMN1; SMN2 Q16637 2/20 0.77
CHRM5 P08912 5/20 0.77
CHRM1 P11229 5/20 0.77
CHRM3 P20309 5/20 0.77
CHRM4 P08173 4/20 0.77
MEN1 O00255 3/20 0.77
KMT2A Q03164 3/20 0.77
TSHR P16473 2/20 0.77
CYP3A4 P08684 1/20 0.66
CYP2C9 P11712 1/20 0.66
HIF1A Q16665 1/20 0.66
HSD17B10 Q99714 1/20 0.66
KDM4E B2RXH2 1/20 0.65
LMNA P02545 1/20 0.65
POLB P06746 1/20 0.65
ADRA2C P18825 1/20 0.65

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
Atropine Oxide SCHEMBL98985 1.00 CYP2C19 (1.00) CYP2C19CHRM2BLMPABPC1SMN1; SMN2
Atropine Oxide SCHEMBL29369999 1.00 CYP2C19 (1.00) CYP2C19CHRM2BLMPABPC1SMN1; SMN2
Atropine Oxide SCHEMBL667605 0.99 CYP2C19 (0.98) CYP2C19CHRM2BLMPABPC1SMN1; SMN2
Atropine Oxide SCHEMBL1490299 0.98 CYP2C19 (0.95) CYP2C19CHRM2BLMPABPC1SMN1; SMN2
Atropine Oxide SCHEMBL1490302 0.98 CYP2C19 (0.95) CYP2C19CHRM2BLMPABPC1SMN1; SMN2
Methylatropine SCHEMBL824874 0.90 CHRM2 (1.00) CYP2C19CHRM2BLMPABPC1SMN1; SMN2
Methylatropine SCHEMBL34463463 0.90 CHRM2 (1.00) CYP2C19CHRM2BLMPABPC1SMN1; SMN2
Methylatropine SCHEMBL1321572 0.89 BLM (1.00) CYP2C19CHRM2BLMPABPC1SMN1; SMN2
Methylatropine SCHEMBL30647266 0.89 BLM (1.00) CYP2C19CHRM2BLMPABPC1SMN1; SMN2
Methylatropine SCHEMBL29389879 0.89 PABPC1 (1.00) CYP2C19CHRM2BLMPABPC1SMN1; 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 263 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240191267-A1 Tropane Alkaloid Transporters and Methods of Making Tropane Alkaloids Using the Same HERCULES CAPITAL, INC., AS AGENT 2024-06-13 US claimed
EP-4314301-A1 TROPANE ALKALOID TRANSPORTERS AND METHODS OF MAKING TROPANE ALKALOIDS USING THE SAME The Board of Trustees of the Leland Stanford Junior University (US) 2024-02-07 EP claimed
CN-117500928-A Tropane alkaloid transporter and method for producing tropane alkaloid using same 小利兰·斯坦福大学托管委员会 2024-02-02 CN claimed
WO-2022204283-A1 TROPANE ALKALOID TRANSPORTERS AND METHODS OF MAKING TROPANE ALKALOIDS USING THE SAME THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2022-09-29 WO claimed
US-10123996-B2 Macrocyclic lactone compounds and methods for their use ELIXIR MEDICAL CORPORATION (US) 2018-11-13 US claimed
US-20170119741-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION 2017-05-04 US claimed
US-20150352089-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION 2015-12-10 US claimed
US-20130230571-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION (US) 2013-09-05 US claimed
EP-2624834-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE Elixir Medical Corporation (US) 2013-08-14 EP claimed
EP-1480677-B8 COMPOSITION FOR STABILIZING HYALURONIC ACID CARL ZEISS MEDITEC SAS (FR) 2012-05-23 EP claimed
EP-1480677-A2 COMPOSITION FOR STABILIZING HYALURONIC ACID IOLTECH (FR) 2004-12-01 EP claimed
US-6784194-B2 FOR INHIBITING EFFECTS OF EXOGENOUS NEUROTOXIC OR NEUROTOXINIC PRODUCTS IN WARM-BLOODED ANIMALS SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES (S.C.R.A.S.) (FR) 2004-08-31 US claimed
EP-0956019-B1 NOVEL THERAPEUTIC APPLICATION OF A THIENYCYCLOHEXYLAMINE DERIVATIVE SOD CONSEILS RECH APPLIC (FR) 2003-10-15 EP claimed
US-20030133986-A1 Compositions for stabilizing poly (carboxylic acids) TSAO FU-PAO (US) 2003-07-17 US claimed
WO-2003043660-A2 COMPOSITION FOR STABILIZING HYALURONIC ACID NOVARTIS AG (CH) 2003-05-30 WO claimed
US-20010056091-A1 Therapeutic use of a thienylcyclohexylamine derivative SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES (S.C.R.A.S) 2001-12-27 US claimed
CN-1294519-A Pharmaceutical composition containing a compound having an activity of promoting the absorption of an active ingredient INPHARMA SA (CH) 2001-05-09 CN claimed
US-6207685-B1 INHIBITING EFFECTS OF EXOGENOUS NEUROTOXIC OR NEUROTOXINIC PRODUCTS IN WARM-BLOODED ANIMALS BY ADMINISTERING 2-METHYL-1-(1-PIPERIDINYL)-1-(2-THIENYL)-CYCLOHEXANE IN PURE RACEMIC, DIASTEREOISOMERIC OR ENANTIOMERIC FORM SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES (S.C.R.A.S.) (FR) 2001-03-27 US claimed
EP-1073470-A1 PHARMACEUTICAL COMPOSITIONS CONTAINING COMPOUNDS WITH ACTIVITY FOR THE ENHANCEMENT OF ABSORPTION OF ACTIVE INGREDIENTS INPHARMA S.A. (CH) 2001-02-07 EP claimed
WO-2000048636-A1 PHARMACEUTICAL COMPOSITIONS CONTAINING COMPOUNDS WITH ACTIVITY FOR THE ENHANCEMENT OF ABSORPTION OF ACTIVE INGREDIENTS INPHARMA S.A. (CH) 2000-08-24 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 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-10123996-B2 Macrocyclic lactone compounds and methods for their use CHRM2, CHRM1, CHRM5 CYP2C19 216/4885CHRM2 1/4885BLM 2554/4885
US-20170119741-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE CHRM2, CHRM1, CHRM5 CYP2C19 98/4885CHRM2 1/4885BLM 3151/4885
US-20150352089-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE CHRM2, CHRM1, CHRM5 CYP2C19 107/4885CHRM2 1/4885BLM 3140/4885

“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.