Butylamine

Butylamine

SCHEMBL2800745

CCCCN.CCCCN.CCCCN.CCCCN.O

nearest known ligand 0.67

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO

The experimentally established mechanism targets of Butylamine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 known ✓ O00255 1/20 0.67
THRB known ✓ P10828 1/20 0.43
DNM1 Q05193 9/20 0.67
TSHR P16473 3/20 0.67
KMT2A Q03164 1/20 0.67
ALDH1A1 P00352 1/20 0.67
EPHX1 P07099 1/20 0.67
LMNA P02545 1/20 0.46
NFKB1 P19838 1/20 0.46
GABBR2 O75899 1/20 0.43
GABRR1 P24046 1/20 0.43
GABBR1 Q9UBS5 1/20 0.43
CA12 O43570 2/20 0.43
CA1 P00915 2/20 0.43
CA2 P00918 2/20 0.43
CA3 P07451 2/20 0.43
CA4 P22748 2/20 0.43
CA6 P23280 2/20 0.43
CA5A P35218 2/20 0.43
CA7 P43166 2/20 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
Butylamine SCHEMBL103293 1.00
Butylamine SCHEMBL5001577 1.00 DNM1 (0.67) DNM1TSHRMEN1KMT2AALDH1A1
Butylamine SCHEMBL27308164 1.00
Butylamine SCHEMBL6933505 1.00
Butylamine SCHEMBL2051232 0.96
Butylamine SCHEMBL4335242 0.96
Butylamine SCHEMBL10449621 0.96
Butylamine SCHEMBL896455 0.96
Butylamine SCHEMBL571241 0.96
Butylamine SCHEMBL4335244 0.96

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115103930-A Method for reducing or preventing corrosion or fouling by acidic compounds 栗田工业株式会社 2022-09-23 CN claimed
CN-114292614-A Preparation method of modified silicon dioxide-epoxy resin composite slurry 西陇科学股份有限公司 2022-04-08 CN claimed
US-7687622-B2 Process for preparing quetiapine fumarate TEVA PHARMACEUTICAL INDUSTRIES, LTD (IL) 2010-03-30 US claimed
EP-0704094-B1 POLYMERS FOR OPTICAL DEVICES CAMBRIDGE DISPLAY TECH LTD (GB) 2001-08-08 EP claimed
US-5514878-A Polymers for electroluminescent devices CAMBRIDGE DISPLAY TECHNOLOGY LIMITED (GB) 1996-05-07 US claimed
EP-0704094-A1 POLYMERS FOR OPTICAL DEVICES Cambridge Display Technology Limited (GB) 1996-04-03 EP claimed
WO-1994029883-A1 POLYMERS FOR OPTICAL DEVICES CAMBRIDGE DISPLAY TECHNOLOGY LIMITED (GB) 1994-12-22 WO claimed
CN-120039837-A Two-dimensional vanadium-based nitride electrode material for water-based ion battery, and preparation method and application thereof 江西科技师范大学 2025-05-27 CN disclosed
CN-114728265-B Particulate water absorbing agent and method for producing same 株式会社日本触媒 2025-05-02 CN disclosed
CN-119497822-A Immunoassay method based on carbon nanomaterial and method for detecting target antigen by immunoassay method 李知勋 2025-02-21 CN disclosed
CN-119371422-A Methods for preparing Toll-like receptor modulator compounds 吉利德科学公司 2025-01-28 CN disclosed
CN-119335811-A Resist composition and pattern forming method 湖北鼎龙控股股份有限公司 2025-01-21 CN disclosed
CN-114341217-B Aqueous resin composition, aqueous paint, and plastic molded article coated with the aqueous paint DIC株式会社 2024-12-27 CN disclosed
US-20130245043-A1 SUBSTITUTED IMIDAZOPYRIMIDIN-5(6H)-ONES AS ALLOSTERIC MODULATORS OF MGLUR5 RECEPTORS NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR 2013-09-19 US disclosed
US-20130224876-A1 A METHOD AND DEVICE FOR DETECTING ALKYLATING AGENTS Univeristy College Cardiff Consultants Limited 2013-08-29 US disclosed
US-7767806-B2 Hyaluronic acid modification products and drug carriers using them CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2010-08-03 US disclosed
US-20070031503-A1 encapsulates low molecular weight drugs and provides sustained-release over long term, control of blood residence, dispersible in aqueous solution, and improved biocompatibility; hyaluronidase resistance CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2007-02-08 US disclosed
EP-1666518-A1 HYALURONIC ACID MODIFICATION PRODUCTS AND DRUG CARRIERS USING THEM CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2006-06-07 EP disclosed
EP-0536324-B1 METHOD FOR FORMING AN AMINO ACID THIOHYDANTOIN USING AN N-SUBSTITUTED KETENIMINE ACTIVATOR PERKIN ELMER CORP (US) 1998-11-25 EP disclosed
US-5051368-A Method for forming an amino acid thiohydantoin using an N-substituted ketenimine activator APPLIED BIOSYSTEMS, INC. (US) 1991-09-24 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-20070031503-A1 encapsulates low molecular weight drugs and provides sustained-release over long term, control of blood residence, dispersible in aqueous solution, and improved biocompatibility; hyaluronidase resistance CD44, VEGFA, MMP1 MEN1 2717/4885THRB 3257/4885DNM1 4443/4885
US-20130245043-A1 SUBSTITUTED IMIDAZOPYRIMIDIN-5(6H)-ONES AS ALLOSTERIC MODULATORS OF MGLUR5 RECEPTORS GRM5, GRIK5, GRM3 MEN1 4450/4885THRB 678/4885DNM1 663/4885

“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.