SCHEMBL8048422

SCHEMBL8048422

CC(C)COc1ccc(CO)cc1

nearest known ligand 0.53

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
MAPT P10636 3/20 0.53
MEN1 O00255 2/20 0.53
KMT2A Q03164 2/20 0.53
ALOX12 P18054 1/20 0.53
POLB P06746 2/20 0.49
HPGD P15428 2/20 0.49
XBP1 P17861 1/20 0.49
ACACB O00763 5/20 0.48
SMN1; SMN2 Q16637 1/20 0.48
LMNA P02545 2/20 0.46
NR1H4 Q96RI1 1/20 0.45
LTA4H P09960 1/20 0.45
ALDH1A1 P00352 2/20 0.44
KDM4E B2RXH2 1/20 0.44
CYP2C9 P11712 1/20 0.44
CYP2C19 P33261 1/20 0.44
NPSR1 Q6W5P4 1/20 0.43
TARBP2 Q15633 1/20 0.43

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
SCHEMBL1628642 0.86 LMNA (0.62) MAPTMEN1KMT2AALOX12POLB
SCHEMBL123415 0.84 MAPT (0.55) MAPTMEN1KMT2AALOX12POLB
SCHEMBL8047274 0.84 ACACB (0.52) MAPTMEN1KMT2AALOX12POLB
SCHEMBL15114294 0.83 LMNA (0.57) MAPTMEN1KMT2AALOX12POLB
SCHEMBL16902890 0.82 PPARG (0.41) MAPTMEN1KMT2AALOX12POLB
SCHEMBL10916977 0.81 LTA4H (0.40) MAPTMEN1KMT2AALOX12LMNA
SCHEMBL7477540 0.81 NPC1 (0.54) MAPTMEN1KMT2AALOX12POLB
SCHEMBL4527180 0.81 MAPT (0.50) MAPTMEN1KMT2AALOX12POLB
SCHEMBL13155583 0.81 ACACB (0.53) MAPTMEN1KMT2AALOX12POLB
SCHEMBL18608209 0.80 ACACB (0.52) MAPTMEN1KMT2AALOX12POLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107011137-B Synthetic method of pimavanserin intermediate 杭州科耀医药科技有限公司 2020-09-11 CN claimed
CN-111517966-A Method for synthesizing p-isobutoxybenzylamine 杭州益至生物科技有限公司 2020-08-11 CN claimed
US-20240299559-A1 COMPOUNDS THAT MEDIATE PROTEIN DEGRADATION AND METHODS OF USE THEREOF MONTE ROSA THERAPEUTICS AG (CH) 2024-09-12 US disclosed
US-11840515-B2 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 PHARMACEUTICALS INC. (US) 2023-12-12 US disclosed
WO-2023069700-A1 COMPOUNDS THAT MEDIATE PROTEIN DEGRADATION AND METHODS OF USE THEREOF MONTE ROSA THERAPEUTICS, INC. (US) 2023-04-27 WO disclosed
US-11440884-B2 Compounds, salts thereof and methods for treatment of diseases ACADIA PHARMACEUTICALS INC. (US) 2022-09-13 US disclosed
US-20220024871-A1 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 PHARMACEUTICALS INC. 2022-01-27 US 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
CN-107848972-B Process for the preparation of N- (4-fluorobenzyl) -N- (1-methylpiperidin-4-yl) -N' - (4- (2-methylpropyloxy) phenylmethyl) urea and its tartrate salt and polymorph C 阿卡蒂亚药品公司 2021-06-18 CN disclosed
US-20210122713-A1 COMPOUNDS, SALTS THEREOF AND METHODS FOR TREATMENT OF DISEASES ACADIA PHARMACEUTICALS INC. (US) 2021-04-29 US disclosed
US-20210122713-A1 COMPOUNDS, SALTS THEREOF AND METHODS FOR TREATMENT OF DISEASES ACADIA PHARMACEUTICALS INC. (US) 2021-04-29 US disclosed
EP-3325444-A1 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 Pharmaceuticals Inc. (US) 2018-05-30 EP disclosed
CN-107848972-A For preparing N (4 luorobenzyl) N (base of 1 methyl piperidine 4) N ' (4 (2 methyl propoxyl group) phenyl methyl) ureas and its tartrate and polymorphic C method 阿卡蒂亚药品公司 2018-03-27 CN disclosed
US-20180037549-A1 PROCESSES AND INTERMEDIATES FOR THE PREPARATION OF PIMAVANSERIN TAPI CROATIA INDUSTRIES LTD (HR) 2018-02-08 US disclosed
US-20180037549-A1 PROCESSES AND INTERMEDIATES FOR THE PREPARATION OF PIMAVANSERIN TAPI CROATIA INDUSTRIES LTD (HR) 2018-02-08 US disclosed
US-20180037549-A1 PROCESSES AND INTERMEDIATES FOR THE PREPARATION OF PIMAVANSERIN TAPI CROATIA INDUSTRIES LTD (HR) 2018-02-08 US disclosed
EP-3271018-A1 PROCESSES AND INTERMEDIATES FOR THE PREPARATION OF PIMAVANSERIN Pliva Hrvatska D.O.O. (HR) 2018-01-24 EP disclosed
WO-2017015272-A1 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 PHARMACEUTICALS INC. (US) 2017-01-26 WO disclosed
WO-2017015272-A1 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 PHARMACEUTICALS INC. (US) 2017-01-26 WO disclosed
US-6106999-A SENSITIVITY TO GENERAL-PURPOSE VISIBLE LIGHT LASER, SO THAT HIGH-SPEED SCANNING EXPOSURE IS POSSIBLE BY LASER, AND EXTREMELY FINE HIGH RESOLUTION CAN BE OBTAINED; CAN BE USED FOR COATING OR PRINTING UNDER SAFELIGHT IRRADIATING CONDITIONS MITSUI CHEMICALS (JP) 2000-08-22 US 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 (6 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-11840515-B2 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 NR3C2, NR2C2, CYP4A22 MAPT 4837/4885MEN1 4247/4885KMT2A 797/4885
US-20220024871-A1 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 NR3C2, NR2C2, CYP4A22 MAPT 4837/4885MEN1 4241/4885KMT2A 795/4885
US-11440884-B2 Compounds, salts thereof and methods for treatment of diseases SLC10A1, VHL, CYP11B2 MAPT 1266/4885MEN1 264/4885KMT2A 3216/4885
US-20210122713-A1 COMPOUNDS, SALTS THEREOF AND METHODS FOR TREATMENT OF DISEASES SLC10A1, VHL, CYP11B2 MAPT 1266/4885MEN1 264/4885KMT2A 3216/4885
US-20240299559-A1 COMPOUNDS THAT MEDIATE PROTEIN DEGRADATION AND METHODS OF USE THEREOF CDK2, SKP2, CDK1 MAPT 3248/4885MEN1 2754/4885KMT2A 2021/4885
US-20180037549-A1 PROCESSES AND INTERMEDIATES FOR THE PREPARATION OF PIMAVANSERIN PIM1, PIM3, PIM2 MAPT 2923/4885MEN1 3691/4885KMT2A 1480/4885

“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.