SCHEMBL1491229

SCHEMBL1491229

OCCN1CCN(C(c2ccccc2)c2ccccc2)CC1

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
OPRD1 P41143 3/20 0.65
OPRM1 P35372 3/20 0.63
KMT2A Q03164 2/20 0.63
MEN1 O00255 1/20 0.63
DRD3 P35462 4/20 0.62
CHRM2 P08172 3/20 0.62
ADRA2A P08913 3/20 0.62
HTR2A P28223 3/20 0.62
HRH1 P35367 3/20 0.62
HTR2B P41595 3/20 0.62
KCNH2 Q12809 3/20 0.62
CYP2D6 P10635 3/20 0.62
DRD2 P14416 3/20 0.62
ABCB11 O95342 2/20 0.62
ADRA2B P18089 2/20 0.62
ADRA2C P18825 2/20 0.62
ADRA1A P35348 2/20 0.62
OPRK1 P41145 2/20 0.62
DRD4 P21917 1/20 0.62
HRH2 P25021 1/20 0.62

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
SCHEMBL10367443 0.94 DRD3 (0.60) OPRD1OPRM1KMT2AMEN1DRD3
SCHEMBL1405261 0.91 DRD3 (0.76) OPRD1OPRM1KMT2AMEN1DRD3
SCHEMBL20039912 0.91 OPRD1 (0.64) OPRD1OPRM1KMT2AMEN1DRD3
SCHEMBL13845055 0.91 DRD3 (0.76) OPRD1OPRM1KMT2AMEN1DRD3
SCHEMBL6618656 0.90 DRD3 (0.63) OPRD1OPRM1KMT2AMEN1DRD3
Hydrochloric Acid SCHEMBL5113093 0.89 DRD3 (0.74) OPRD1OPRM1KMT2AMEN1DRD3
SCHEMBL6617567 0.88 DRD2 (0.63) OPRD1OPRM1KMT2AMEN1DRD3
Hydrochloric Acid SCHEMBL6475984 0.88 DRD3 (0.73) OPRD1OPRM1KMT2AMEN1DRD3
SCHEMBL6617019 0.87 DRD2 (0.62) OPRD1OPRM1KMT2AMEN1DRD3
Decloxizine SCHEMBL2110441 0.84 HRH1 (0.85) OPRD1OPRM1KMT2AMEN1DRD3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117720457-A Manidipine hydrochloride process impurity m-nifedipine and preparation method and application thereof 成都大学 2024-03-19 CN claimed
CN-103351362-A Preparation method of manidipine intermediate 2-(4-diphenylmethyl piperazinyl)ethyl acetoacetate ZHANGJIAGANG WEISHENG BIOLOG PHARCEUTICAL CO LTD 2013-10-16 CN claimed
CN-103214434-A Improved method of 1-diphenylmethyl-4-(2-hydroxyethyl) piperazine synthesis technology ZHANGJIAGANG WEISHENG BIOLOG MEDICAL CO LTD 2013-07-24 CN claimed
EP-1157016-B1 A PROCESS FOR THE PREPARATION OF 2- 2- 4-(DIPHENYLMETHYL)-1-PIPERAZINYL]ETHOXY ACETIC ACID COMPOUNDS OR SALTS THEREOF GEA FARMACEUTISK FABRIK AS (DK) 2003-10-08 EP claimed
EP-1157016-A1 A PROCESS FOR THE PREPARATION OF 2- 2- 4-(DIPHENYLMETHYL)-1-PIPERAZINYL]ETHOXY ACETIC ACID COMPOUNDS OR SALTS THEREOF A/S GEA Farmaceutisk Fabrik (DK) 2001-11-28 EP claimed
WO-2000052000-A1 A PROCESS FOR THE PREPARATION OF 2-{2-[4-(DIPHENYLMETHYL)-1-PIPERAZINYL]ETHOXY}ACETIC ACID COMPOUNDS OR SALTS THEREOF A/S GEA FARMACEUTISK FABRIK (DK) 2000-09-08 WO claimed
US-5644059-A REACTION OF KETONE WITH ACRYLAMIDE AND AMMONIA OR AMMONIUM SALT FUJIREBIO INC. (JP) 1997-07-01 US claimed
EP-0488345-A1 1,4-Dihydropyridine derivatives and methods of producing the same FUJIREBIO INC. (JP) 1992-06-03 EP claimed
JP-9278751-A None JP disclosed
CN-117720457-A Manidipine hydrochloride process impurity m-nifedipine and preparation method and application thereof 成都大学 2024-03-19 CN disclosed
CN-115572253-A Synthesis process of manidipine hydrochloride raw material medicine 许昌恒生制药有限公司 2023-01-06 CN disclosed
CN-115403512-A Method for controlling key impurities of manidipine hydrochloride raw material medicine 许昌恒生制药有限公司 2022-11-29 CN disclosed
US-20220193020-A1 Pharmaceutical Composition Comprising Trimebutine or Pharmaceutically Acceptable Salt Thereof as an Active Ingredient For Prevention or Treatment of Cancer DAEGU-GYEONGBUK MEDICAL INNOVATION FOUNDATION (KR) 2022-06-23 US disclosed
CN-106518806-A Preparation method for manidipine intermediate 2-(4-diphenylmethyl piperazine)ethyl acetoacetate 张家港威胜生物医药有限公司 2017-03-22 CN disclosed
EP-0094159-B1 DIHYDROPYRIDINE DERIVATIVES, THEIR PRODUCTION AND USE Takeda Chemical Industries, Ltd. (JP) 1990-03-14 EP disclosed
US-4892875-A HYPOTENSIVE, RENAL VASODILATION TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1990-01-09 US disclosed
WO-1988002750-A1 1,4-DIHYDROPYRIDINE BYK GULDEN LOMBERG CHEMISCHE FABRIK GMBH (DE) 1988-04-21 WO disclosed
US-4603135-A HYPOTENSIVE AGENTS TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1986-07-29 US disclosed
EP-0138505-A2 Dihydropyridine derivatives, their production and use Takeda Chemical Industries, Ltd. (JP) 1985-04-24 EP disclosed
EP-0094159-A1 Dihydropyridine derivatives, their production and use Takeda Chemical Industries, Ltd. (JP) 1983-11-16 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-20220193020-A1 Pharmaceutical Composition Comprising Trimebutine or Pharmaceutically Acceptable Salt Thereof as an Active Ingredient For Prevention or Treatment of Cancer TRIM59, TRIM24, WASHC5 OPRD1 3894/4885OPRM1 4182/4885KMT2A 1171/4885

“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.