SCHEMBL1861653

SCHEMBL1861653

CCCN1CCN(CCCN)CC1

nearest known ligand 0.75

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
KEAP1 Q14145 1/20 0.54
SMN1; SMN2 Q16637 1/20 0.54
ALOX15 P16050 1/20 0.50
GNAI3 P08754 1/20 0.48
GNAO1 P09471 1/20 0.48
GNAI1 P63096 1/20 0.48
SIGMAR1 Q99720 2/20 0.47
CYP2D6 P10635 1/20 0.47
HSD17B10 Q99714 1/20 0.44
ACE2 Q9BYF1 1/20 0.44

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
SCHEMBL4392316 0.93 GNAI3 (0.52) KEAP1SMN1; SMN2ALOX15GNAI3GNAO1
SCHEMBL4395108 0.90 KEAP1 (0.54) KEAP1SMN1; SMN2ALOX15GNAI3GNAO1
SCHEMBL6277287 0.88 GNAI3 (0.63) KEAP1SMN1; SMN2ALOX15GNAI3GNAO1
SCHEMBL101501 0.87 KEAP1 (0.67) KEAP1SMN1; SMN2ALOX15SIGMAR1CYP2D6
SCHEMBL1616800 0.87
SCHEMBL1935309 0.85 KEAP1 (0.54) KEAP1SMN1; SMN2ALOX15GNAI3GNAO1
SCHEMBL4396498 0.84 ALOX15 (0.72) ALOX15GNAI3GNAO1GNAI1SIGMAR1
SCHEMBL15329386 0.84 KEAP1 (0.64) KEAP1SMN1; SMN2ALOX15SIGMAR1CYP2D6
SCHEMBL6659154 0.84 GNAI3 (0.50) GNAI3GNAO1GNAI1SIGMAR1
SCHEMBL6656231 0.84 GNAI3 (0.56) GNAI3GNAO1GNAI1SIGMAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9328093-B2 Selective inhibitors of ubiquitin specific protease 7, the pharmaceutical compositions thereof and their therapeutic applications HYBRIGENICS SA (FR) 2016-05-03 US claimed
US-20150072973-A1 NOVEL SELECTIVE INHIBITORS OF UBIQUITIN SPECIFIC PROTEASE 7, THE PHARMACEUTICAL COMPOSITIONS THEREOF AND THEIR THERAPEUTIC APPLICATIONS HYBRIGENICS SA (FR) 2015-03-12 US claimed
WO-2024136309-A1 IONIZABLE LIPID AND USE THEREOF GREEN CROSS CORPORATION (KR) 2024-06-27 WO disclosed
CN-114957279-B Dihydrothieno [2,3-e ] indazole compound, pharmaceutical composition and application 中国人民解放军军事科学院军事医学研究院 2023-08-01 CN disclosed
WO-2023133089-A1 IONIZABLE LIPIDS FOR MULTIPLE ORGAN TARGETING MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2023-07-13 WO disclosed
EP-3660004-B1 COMPOUNDS AND METHODS FOR THE TARGETED DEGRADATION OF ANDROGEN RECEPTOR ARVINAS OPERATIONS INC (US) 2023-02-22 EP disclosed
CN-114957279-A Dihydrothieno [2,3-e ] indazole compound, pharmaceutical composition and application 中国人民解放军军事科学院军事医学研究院 2022-08-30 CN disclosed
WO-2018140809-A1 MODULATORS OF ESTROGEN RECEPTOR PROTEOLYSIS AND ASSOCIATED METHODS OF USE Arvinas, Inc. (US) 2018-08-02 WO disclosed
WO-2018118598-A1 COMPOUNDS AND METHODS FOR THE TARGETED DEGRADATION OF FETAL LIVER KINASE POLYPEPTIDES Arvinas, Inc. (US) 2018-06-28 WO disclosed
WO-2018102725-A1 TETRAHYDRONAPHTHALENE AND TETRAHYDROISOQUINOLINE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS Arvinas, Inc. (US) 2018-06-07 WO disclosed
US-9884863-B2 STAT3 inhibitor BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2018-02-06 US disclosed
US-20070054084-A1 Optical recording medium and compound used for the same MITSUI CHEMICALS, INC. (JP) 2007-03-08 US disclosed
EP-1672626-A1 OPTICAL RECORDING MEDIUM AND COMPOUND USED IN THE OPTICAL RECORDING MEDIUM Mitsui Chemicals, Inc. (JP) 2006-06-21 EP disclosed
US-6479482-B2 4-(3-((((3-(4-((3-METHYLBUTYL)AMINO)-1-PIPERIDINYL)PROPYL) -AMINO)-CARBONYL)AMINO)PHENYL)-1,4-DIHYDRO-2,6-DIMETHYL-3,5 -PYRIDINEDICARBOXYLIC ACID, DIMETHYL ESTER DIHYDROCHLORIDE, FOR EXAMPLE; ANOREXIANT; NEUROPEPTIDE Y (NPY) BRISTOL-MYERS SQUIBB COMPANY 2002-11-12 US disclosed
US-20020019384-A1 Alkylamine derivatives of dihydropyridine NPY antagonists BRISTOL-MYERS SQUIBB COMPANY 2002-02-14 US disclosed
WO-2001085173-A1 ALKYLAMINE DERIVATIVES OF DIHYDROPYRIDINE NPY ANTAGONISTS BRISTOL-MYERS SQUIBB COMPANY (US) 2001-11-15 WO disclosed
EP-0629607-B1 Compounds containing tertiary amino groups, process for their preparation and use as catalyst BAYER AG (DE) 2001-10-31 EP disclosed
US-5482979-A CATALYSTS OR PROMOTERS FOR POLYURETHANE FOAMS BAYER AKTIENGESELLSCHAFT (DE) 1996-01-09 US disclosed
EP-0629607-A2 Compounds containing tertiary amino groups, process for their preparation and use as catalyst BAYER AG (DE) 1994-12-21 EP disclosed
US-4992150-A Telomer with alpha-olefin;oil and fuel additive NIPPON OIL CO, LTD. (JP) 1991-02-12 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 (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-20020019384-A1 Alkylamine derivatives of dihydropyridine NPY antagonists NPY1R, NPY2R, NPY4R KEAP1 3493/4885SMN1; SMN2 2849/4885ALOX15 2207/4885
US-20150072973-A1 NOVEL SELECTIVE INHIBITORS OF UBIQUITIN SPECIFIC PROTEASE 7, THE PHARMACEUTICAL COMPOSITIONS THEREOF AND THEIR THERAPEUTIC APPLICATIONS USP7, SENP7, PSMA7 KEAP1 637/4885SMN1; SMN2 2877/4885ALOX15 4233/4885

“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.