Cycrimine

Cycrimine

SCHEMBL1235292

Cl.OC(CCN1CCCCC1)(c1ccccc1)C1CCCC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CHRM1

The experimentally established mechanism targets of Cycrimine. 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
CHRM1 known ✓ P11229 8/20 1.00
CHRM2 P08172 8/20 1.00
CHRM3 P20309 5/20 1.00
CHRM4 P08173 4/20 1.00
CHRM5 P08912 3/20 1.00
MAPT P10636 2/20 1.00
BLM P54132 1/20 1.00
PMP22 Q01453 1/20 1.00
CYP2D6 P10635 6/20 0.97
KCNH2 Q12809 6/20 0.97
HTR1A P08908 2/20 0.97
OPRM1 P35372 2/20 0.97
HRH1 P35367 2/20 0.97
CYP3A4 P08684 2/20 0.97
TSHR P16473 2/20 0.97
GRIN2D O15399 1/20 0.97
GRIN3B O60391 1/20 0.97
GRIN1 Q05586 1/20 0.97
GRIN2A Q12879 1/20 0.97
GRIN2B Q13224 1/20 0.97

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
Trihexyphenidyl SCHEMBL30061697 1.00 CHRM2 (1.00) CHRM2CHRM1CHRM3CHRM4CHRM5
Procyclidine SCHEMBL121684 1.00 CHRM2 (1.00) CHRM2CHRM1CHRM3CHRM4CHRM5
Trihexyphenidyl SCHEMBL5502902 1.00 CHRM2 (1.00) CHRM2CHRM1CHRM3CHRM4CHRM5
Trihexyphenidyl SCHEMBL42410 1.00 CHRM2 (1.00) CHRM2CHRM1CHRM3CHRM4CHRM5
Trihexyphenidyl SCHEMBL1320615 0.99 CHRM2 (1.00) CHRM2CHRM1CHRM3CHRM4CHRM5
Procyclidine SCHEMBL147344 0.99 CHRM2 (1.00) CHRM2CHRM1CHRM3CHRM4CHRM5
Trihexyphenidyl SCHEMBL34646 0.99 CHRM2 (1.00) CHRM2CHRM1CHRM3CHRM4CHRM5
Cycrimine SCHEMBL249004 0.99 CHRM2 (1.00) CHRM2CHRM1CHRM3CHRM4CHRM5
Trihexyphenidyl SCHEMBL34645 0.99 CHRM2 (1.00) CHRM2CHRM1CHRM3CHRM4CHRM5
(S)-Procyclidine SCHEMBL519431 0.99 CHRM2 (1.00) CHRM2CHRM1CHRM3CHRM4CHRM5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260114475-A1 ANIMAL FOOD COMPOSITIONS WITH IMPROVED PALATABILITY AND CUSTOMIZABILITY, AND METHODS FOR PREPARING THE SAME MARS, INCORPORATED (US) 2026-04-30 US disclosed
EP-4593631-A1 ANIMAL FOOD COMPOSITIONS WITH IMPROVED PALATABILITY AND CUSTOMIZABILITY, AND METHODS FOR PREPARING THE SAME Mars, Incorporated (US) 2025-08-06 EP disclosed
US-20240145031-A1 Methods and devices for drug repositioning and drug repurposing as nuclear receptor modulators Precision Medicine Lab (NL) 2024-05-02 US disclosed
WO-2024073025-A1 ANIMAL FOOD COMPOSITIONS WITH IMPROVED PALATABILITY AND CUSTOMIZABILITY, AND METHODS FOR PREPARING THE SAME MARS, INCORPORATED (US) 2024-04-04 WO disclosed
EP-4344552-A1 ANIMAL FOOD COMPOSITIONS WITH IMPROVED PALATABILITY, AND METHODS FOR PREPARING THE SAME MARS, INCORPORATED (US) 2024-04-03 EP disclosed
US-20210346385-A1 TASTE-MASKED DOSAGE FORMS DEEP OCEAN CAPITAL MANAGEMENT LP 2021-11-11 US disclosed
US-20210290771-A1 ENGINEERED RECEPTOR/LIGAND SYSTEM FOR DELIVERY OF THERAPEUTIC AGENTS UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED (US) 2021-09-23 US disclosed
US-11000597-B2 Engineered receptor/ligand system for delivery of therapeutic agents UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED (US) 2021-05-11 US disclosed
US-20200197310-A1 Technology for Preparation of Macromolecular Microspheres NEXBIO, INC. 2020-06-25 US disclosed
WO-2020112814-A1 DEVICES, SYSTEMS, AND METHODS TO MONITOR SUBJECT COMPLIANCE WITH A PHARMACEUTICAL TREATMENT REGIMEN SAKAYA JAQUELINE MBWILLE (US) 2020-06-04 WO disclosed
EP-0055043-B1 6,7,8,9-TETRAHYDRO-3H-BENZ(E)INDOLAMINE DERIVATIVES, PROCESSES FOR THEIR PREPARATION AND INTERMEDIATES USED THEREIN, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE INDOLAMINE DERIVATIVES AYERST, MCKENNA AND HARRISON INC. (CA) 1985-01-23 EP disclosed
EP-0034894-B1 2-(1-PIPERAZINYL)-2,4,6-CYCLOHEPTATRIEN-1-ONE DERIVATIVES, PROCESSES FOR THEIR PREPARATION, INTERMEDIATES USED IN THE PROCESSES AND THE PREPARATION THEREOF AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE DERIVATIVES AYERST, MCKENNA AND HARRISON INC. (CA) 1984-09-12 EP disclosed
US-4470990-A 6,7,8,9-Tetrahydronaphtho(1,2-B)furan-8-amine derivatives and their use as dopamine receptor stimulants AYERST, MCKENNA & HARRISON INC. (CA) 1984-09-11 US disclosed
US-4469695-A 2-(4-Hydroxyalkyl-1-piperazinyl)-2,4,6-cycloheptatrien-1-one derivatives AYERST, MCKENNA & HARRISON, INC. (CA) 1984-09-04 US disclosed
US-4469693-A 2-(4-Substituted alkyl-1-piperazinyl)-2,4,6-cycloheptatrien-1-one derivatives AYERST, MCKENNA & HARRISON INC. (CA) 1984-09-04 US disclosed
US-4469694-A 2-(1-Piperazinyl)-2,4,6-cycloheptatrien-1-one derivatives AYERST, MCKENNA & HARRISON INC. (CA) 1984-09-04 US disclosed
US-4454150-A 6,7,8,9-Tetrahydro-3H-benz(e)indol-7-amines and a method of dopamine receptor stimulation therewith AYERST, MCKENNA & HARRISON INC. (US) 1984-06-12 US disclosed
US-4370341-A 6,7,8,9-Tetrahydro-3H-benz[E]indol-8-amine derivatives AYERST, MCKENNA & HARRISON, LTD. (CA) 1983-01-25 US disclosed
EP-0055043-A2 6,7,8,9-Tetrahydro-3H-benz(e)indolamine derivatives, processes for their preparation and intermediates used therein, and pharmaceutical compositions containing the indolamine derivatives AYERST, MCKENNA AND HARRISON INC. (CA) 1982-06-30 EP disclosed
EP-0034894-A2 2-(1-Piperazinyl)-2,4,6-cycloheptatrien-1-one derivatives, processes for their preparation, intermediates used in the processes and the preparation thereof and pharmaceutical compositions containing the derivatives AYERST, MCKENNA AND HARRISON INC. (CA) 1981-09-02 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 (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-20260114475-A1 ANIMAL FOOD COMPOSITIONS WITH IMPROVED PALATABILITY AND CUSTOMIZABILITY, AND METHODS FOR PREPARING THE SAME PIGS, TAS2R13, CEL CHRM1 2690/4885CHRM2 2576/4885CHRM3 3706/4885

“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.