SCHEMBL10290341

SCHEMBL10290341

CCCCCCCC(=O)N1CCCC1

nearest known ligand 0.96

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
▸ L3MBTL1 Q9Y468 2/20 0.96
▸ MEN1 O00255 2/20 0.92
▸ KMT2A Q03164 2/20 0.92
▸ TDP1 Q9NUW8 1/20 0.92
▸ ATM Q13315 1/20 0.68
▸ GNAI3 P08754 9/20 0.68
▸ GNAI1 P63096 9/20 0.68
▸ GNAO1 P09471 8/20 0.64
▸ POLB P06746 1/20 0.54
▸ MAPT P10636 1/20 0.54

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
SCHEMBL27508518 1.00 L3MBTL1 (0.96) L3MBTL1MEN1KMT2ATDP1ATM
N-(Decanoyl)Pyrrolidine SCHEMBL10755236 1.00 L3MBTL1 (0.96) L3MBTL1MEN1KMT2ATDP1ATM
SCHEMBL28152342 1.00 L3MBTL1 (0.96) L3MBTL1MEN1KMT2ATDP1ATM
SCHEMBL10534175 1.00 L3MBTL1 (0.96) L3MBTL1MEN1KMT2ATDP1ATM
SCHEMBL10534171 1.00 L3MBTL1 (0.96) L3MBTL1MEN1KMT2ATDP1ATM
SCHEMBL10494122 1.00 L3MBTL1 (0.96) L3MBTL1MEN1KMT2ATDP1ATM
SCHEMBL151361 1.00 L3MBTL1 (0.96) L3MBTL1MEN1KMT2ATDP1ATM
N-(Decanoyl)Pyrrolidine SCHEMBL692598 1.00 L3MBTL1 (0.96) L3MBTL1MEN1KMT2ATDP1ATM
SCHEMBL249052 1.00 L3MBTL1 (0.96) L3MBTL1MEN1KMT2ATDP1ATM
SCHEMBL28149836 1.00 L3MBTL1 (0.96) L3MBTL1MEN1KMT2ATDP1ATM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1569831-A Phenol-containing wastewater extraction agent N-octanoyl pentazane and its synthesis method UNIV SHANGHAI (CN) 2005-01-26 — — CN claimed
US-20250361234-A1 COMPOUNDS, COMPOSITIONS, AND METHODS NICO THERAPEUTICS INC (US) 2025-11-27 — — US disclosed
US-20240410034-A1 CYCLIC AMINE MONOAMIDES FOR EXTRACTING URANIUM(VI) AND PLUTONIUM(IV) AND FOR SEPARATING THEM WITHOUT REDUCING PLUTONIUM(IV) Commissariat à l'énergie atomique et aux énergies alternatives (FR) 2024-12-12 — — US disclosed
CN-118354828-A Cyclic amine monoamides for extracting uranium (VI) and plutonium (IV) and for separating them without reduction of the plutonium (IV) 原子能与替代能源委员会 2024-07-16 — — CN disclosed
WO-2023067273-A1 CYCLIC AMINE MONOAMIDES FOR THE EXTRACTION OF URANIUM(VI) AND PLUTONIUM(IV) AND FOR THE SEPARATION THEREOF WITHOUT REDUCTION OF THE PLUTONIUM(IV) COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (FR) 2023-04-27 — — WO disclosed
CN-111995152-B Method for treating high-concentration wastewater generated in synthesis of anisole from methyl sodium sulfate waste residues 浙江大洋生物科技集团股份有限公司 2022-05-13 — — CN disclosed
US-10441581-B2 Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors ARRAY BIOPHARMA INC. (US) 2019-10-15 — — US disclosed
US-20180133207-A1 SUBSTITUTED PYRAZOLO[1,5-A]PYRIDINE COMPOUNDS AS RET KINASE INHIBITORS ARRAY BIOPHARMA INC. 2018-05-17 — — US disclosed
US-9671415-B2 Immunoassay for pyrrolidinophenones RANDOX LABORATORIES LIMITED (GB) 2017-06-06 — — US disclosed
US-20160097783-A1 IMMUNOASSAY FOR PYRROLIDINOPHENONES NORTHERN BANK LIMITED (IE) 2016-04-07 — — US disclosed
US-9012690-B2 Method for producing alcohol and/or amine from amide compound TAKASAGO INTERNATIONAL CORPORATION (JP) 2015-04-21 — — US disclosed
US-20130172619-A1 METHOD FOR PRODUCING ALCOHOL AND/OR AMINE FROM AMIDE COMPOUND TAKASAGO INTERNATIONAL CORPORATION (JP) 2013-07-04 — — US disclosed
CN-102976561-A Technique for treating phenol/anisole-containing production wastewater UNIV TIANJIN POLYTECHNIC 2013-03-20 — — CN disclosed
US-20120041190-A1 MACROCYCLES AS FACTOR XIA INHIBITORS BRISTOL-MYERS SQUIBB COMPANY 2012-02-16 — — US disclosed
CN-1569831-A Phenol-containing wastewater extraction agent N-octanoyl pentazane and its synthesis method UNIV SHANGHAI (CN) 2005-01-26 — — CN disclosed
US-4837026-A Transdermal and systemic preparation and method THERAPEUTIC PATCH RESEARCH N.V. 1989-06-06 — — US disclosed
EP-0240554-A1 TRANSDERMAL AND SYSTEMIC PREPARATION AND METHOD RAJADHYAKSHA, Vithal J. (US) 1987-10-14 — — EP disclosed
WO-1987001935-A1 TRANSDERMAL AND SYSTEMIC PREPARATION AND METHOD RAJADHYAKSHA VITHAL J 1987-04-09 — — 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 (7 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-20120041190-A1 MACROCYCLES AS FACTOR XIA INHIBITORS TFPI, TFPI2, F11 L3MBTL1 4750/4885MEN1 376/4885KMT2A 1111/4885
US-20240410034-A1 CYCLIC AMINE MONOAMIDES FOR EXTRACTING URANIUM(VI) AND PLUTONIUM(IV) AND FOR SEPARATING THEM WITHOUT REDUCING PLUTONIUM(IV) PADI2, PADI4, PADI1 L3MBTL1 3340/4885MEN1 1395/4885KMT2A 1009/4885
US-20250361234-A1 COMPOUNDS, COMPOSITIONS, AND METHODS SARM1, SARS1, TIAM1 L3MBTL1 1416/4885MEN1 1134/4885KMT2A 3835/4885
US-20130172619-A1 METHOD FOR PRODUCING ALCOHOL AND/OR AMINE FROM AMIDE COMPOUND ADH1A, ADH1C, ADH5 L3MBTL1 1593/4885MEN1 2754/4885KMT2A 909/4885
US-20160097783-A1 IMMUNOASSAY FOR PYRROLIDINOPHENONES CYP2D6, CYP2B6, CYP3A43 L3MBTL1 4860/4885MEN1 3835/4885KMT2A 4554/4885
US-10441581-B2 Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors RET, BRAF, RAF1 L3MBTL1 2011/4885MEN1 653/4885KMT2A 1112/4885
US-20180133207-A1 SUBSTITUTED PYRAZOLO[1,5-A]PYRIDINE COMPOUNDS AS RET KINASE INHIBITORS RET, BRAF, RAF1 L3MBTL1 2011/4885MEN1 653/4885KMT2A 1112/4885

“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.

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