SCHEMBL3653016

SCHEMBL3653016

CC(C)COc1ccc(CNC(=O)NC2CCN(C)CC2)cc1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR2A P28223 11/20 0.62
HTR2C P28335 6/20 0.59
HRH3 Q9Y5N1 2/20 0.59
ABCB11 O95342 1/20 0.59
CYP1A2 P05177 1/20 0.59
ADRB2 P07550 1/20 0.59
CHRM2 P08172 1/20 0.59
CHRM1 P11229 1/20 0.59
DRD1 P21728 1/20 0.59
TBXA2R P21731 1/20 0.59
SLC6A2 P23975 1/20 0.59
GPR183 P32249 1/20 0.59
CYP2C19 P33261 1/20 0.59
ADRA1A P35348 1/20 0.59
OPRM1 P35372 1/20 0.59
APLNR P35414 1/20 0.59
DRD3 P35462 1/20 0.59
CX3CR1 P49238 1/20 0.59
SLC6A3 Q01959 1/20 0.59
KCNH2 Q12809 1/20 0.59

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
Cadaverine Tartrate SCHEMBL3529128 0.94 HTR2A (0.56) HTR2AHTR2CHRH3ABCB11CYP1A2
SCHEMBL31707510 0.85 HTR2A (0.58) HTR2AHTR2CHRH3ABCB11CYP1A2
SCHEMBL4980231 0.84 RAB9A (0.74) HRH3RAB9ASMN1; SMN2NPC1MCHR1
SCHEMBL4975779 0.81 DRD4 (0.59) HRH3RAB9ASMN1; SMN2NPC1MCHR1
SCHEMBL4984077 0.81 NPC1 (0.55) HTR2CHRH3RAB9ASMN1; SMN2NPC1
SCHEMBL4978994 0.80 SMN1; SMN2 (0.72) HRH3RAB9ASMN1; SMN2NPC1MCHR1
SCHEMBL31473510 0.80 HTR2A (0.71) HTR2AHTR2CHRH3ABCB11CYP1A2
SCHEMBL8219973 0.80 MAPT (0.64) HTR2AHTR2CHRH3ABCB11CYP1A2
SCHEMBL14263119 0.80 RAB9A (0.54) HRH3RAB9ASMN1; SMN2NPC1MCHR1
SCHEMBL4982545 0.79 MCHR1 (0.66) HTR2AHRH3RAB9ASMN1; SMN2NPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025061176-A1 CYCLOALKANE-SUBSTITUTED AMINE DERIVATIVE, PREPARATION METHOD THEREFOR AND USE THEREOF 上海科技大学 2025-03-27 WO disclosed
CN-119661404-A Cycloalkane substituted amine derivative, preparation method and application thereof 上海科技大学 2025-03-21 CN disclosed
CN-117466803-A Compounds, salts thereof and methods for treating diseases 阿卡蒂亚药品公司 2024-01-30 CN disclosed
CN-111132976-B Compounds, salts thereof and methods for treating diseases 阿卡蒂亚药品公司 2023-08-22 CN disclosed
EP-3325444-B1 METHODS FOR PREPARING N-(4-FLUOROBENZYL)-N-(1-METHYLPIPERIDIN-4-YL)-N'-(4-(2-METHYLPROPYLOXY)PHENYLMETHYL)CARBAMIDE AND ITS TARTRATE SALT AND POLYMORPHIC FORM C ACADIA PHARM INC (US) 2021-07-07 EP disclosed
EP-3828170-A1 METHOD FOR SAFELY PREPARING PIMAVANSERIN AND TARTRATE SALT THEREOF USING TRIPHOSGENE Livzon New North River Pharmaceutical Co., Ltd. (CN) 2021-06-02 EP disclosed
US-10934257-B2 Method for preparing pimavanserin and tartrate thereof by using triphosgene LIVZON NEW NORTH RIVER PHARMACEUTICAL CO., LTD. (CN) 2021-03-02 US disclosed
US-20200369612-A1 Method for Safely Preparing Pimavanserin and Tartrate Thereof by Using Triphosgene LIVZON NEW NORTH RIVER PHARMACEUTICAL CO., LTD. (CN) 2020-11-26 US disclosed
WO-2020020064-A1 METHOD FOR SAFELY PREPARING PIMAVANSERIN AND TARTRATE SALT THEREOF USING TRIPHOSGENE 丽珠集团新北江制药股份有限公司 2020-01-30 WO disclosed
EP-2200610-A2 CO-ADMINISTRATION OF PIMAVANSERIN WITH OTHER AGENTS Acadia Pharmaceuticals Inc. (US) 2010-06-30 EP disclosed
EP-2173343-A1 USE OF PIMAVANSERIN IN THE TREATMENT OF PARKINSON AND SYMPTOMS THEREOF Acadia Pharmaceuticals Inc. (US) 2010-04-14 EP disclosed
WO-2009039460-A2 CO-ADMINISTRATION OF PIMAVANSERIN WITH OTHER AGENTS ACADIA PHARMACEUTICALS, INC. (US) 2009-03-26 WO disclosed
WO-2008144665-A1 USE OF PIMAVANSERIN IN THE TREATMENT OF PARKINSON AND SYMPTOMS THEREOF ACADIA PHARMACEUTICALS INC. (US) 2008-11-27 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 (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-20200369612-A1 Method for Safely Preparing Pimavanserin and Tartrate Thereof by Using Triphosgene PNP, PIM1, TYMP HTR2A 1753/4885HTR2C 2737/4885HRH3 3416/4885
US-10934257-B2 Method for preparing pimavanserin and tartrate thereof by using triphosgene PNP, TYMP, PIM1 HTR2A 1585/4885HTR2C 2514/4885HRH3 3671/4885

“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.