Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Isopropylamine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Isopropylamine SCHEMBL7198176 | 1.00 | ALDH1A1 (0.42) | — | |
| Isopropylamine SCHEMBL11776930 | 1.00 | ALDH1A1 (0.42) | — | |
| Isopropylamine SCHEMBL1243175 | 1.00 | — | — | |
| Isopropylamine SCHEMBL8506223 | 1.00 | — | — | |
| Isopropylamine SCHEMBL25170807 | 0.94 | — | — | |
| Isopropylamine SCHEMBL28876401 | 0.94 | ALDH1A1 (0.39) | — | |
| Isopropylamine SCHEMBL26643084 | 0.94 | — | — | |
| Isopropylamine SCHEMBL30440281 | 0.93 | — | — | |
| Isopropylamine SCHEMBL19813885 | 0.93 | — | — | |
| Isopropylamine SCHEMBL2909 | 0.93 | — | — |
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 1739 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122081268-A | Transaminase mutant and preparation method of chiral amine | — | 2026-05-26 | — | — | CN | claimed |
| CN-118547024-B | Ragliptin intermediate, preparation method and application thereof | Yikelai Biotechnology (Group) Co.,Ltd. (CN) | 2026-05-26 | — | — | CN | claimed |
| EP-4493286-B1 | A SOLID CLEANSING COMPOSITION | UNILEVER IP HOLDINGS B V (NL) | 2026-05-06 | — | — | EP | claimed |
| EP-4417690-A9 | TRANSAMINASE MUTANT AND PREPARATION METHOD FOR CHIRAL AMINE COMPOUND | Asymchem Life Science (Tianjin) Co., Ltd (CN) | 2025-06-18 | — | — | EP | claimed |
| US-20250188388-A1 | A SOLID CLEANSING COMPOSITION | CONOPCO, INC., D/B/A UNILEVER (US) | 2025-06-12 | — | — | US | claimed |
| US-20250177267-A1 | A CLEANSING COMPOSITION | CONOPCO, INC., D/B/A UNILEVER (US) | 2025-06-05 | — | — | US | claimed |
| CN-119931985-A | Enzyme catalytic synthesis method of aminotransferase and remigem intermediate | 江苏阿尔法药业股份有限公司 | 2025-05-06 | — | — | CN | claimed |
| WO-2025059186-A1 | LOW-DIMENSIONAL METAL-HALIDE PEROVSKITES FOR INFRARED, TETRAHERTZ, AND MILLIMETER-WAVE LIGHT DETECTION | YALE UNIVERSITY (US) | 2025-03-20 | — | — | WO | claimed |
| EP-4493285-A1 | A CLEANSING COMPOSITION | Unilever IP Holdings B.V. (NL) | 2025-01-22 | — | — | EP | claimed |
| EP-4493286-A1 | A SOLID CLEANSING COMPOSITION | Unilever IP Holdings B.V. (NL) | 2025-01-22 | — | — | EP | claimed |
| CN-1689695-B | Preparation method of chromatographic particle medium | BEIJING STRONG BIOTECHNOLOGIES INC | 2010-06-23 | — | — | CN | claimed |
| CN-101275375-A | Preparation for interpenetrating meshwork type surface sizing agent | SHANDONG RUITE FINE CHEMICALS (CN) | 2008-10-01 | — | — | CN | claimed |
| CN-101239927-A | Method for preparing monomer of temperature-sensitive polyisopropylacrylamide | RONGHAI SUPERSONIC MEDICINE EN (CN) | 2008-08-13 | — | — | CN | claimed |
| CN-1689695-A | Preparation method of chromatographic particle medium | BEIJING GAORUNTONG BIO TECHNOL (CN) | 2005-11-02 | — | — | CN | claimed |
| US-6376548-B1 | FUNGICIDES; HERBICIDES; INSECTICIDES | ROHM AND HAAS COMPANY | 2002-04-23 | — | — | US | claimed |
| US-5391495-A | Using enzyme or microorganism catalyst | BRISTOL-MYERS SQUIBB COMPANY (US) | 1995-02-21 | — | — | US | claimed |
| CN-1091472-A | The Stereoselective reduction of ketone | BRISTOL MYERS SQUIBB CO (US) | 1994-08-31 | — | — | CN | claimed |
| EP-0596490-A2 | Stereoselective reduction of ketones | Bristol-Myers Squibb Company (US) | 1994-05-11 | — | — | EP | claimed |
| US-4288594-A | Caustic-free process for the production of monochloro-diamino-s-triazines | CIBA-GEIGY CORPORATION (US) | 1981-09-08 | — | — | US | claimed |
| US-4246091-A | COATING A SULFONATED FLUORO POLYMER WITH AN AMINE SALT TO INCREASE THE ION SELECTIVE PERMEABILITY | KUREHA KAGAKU KOGYO KABUSHIKI KAISHA (JP) | 1981-01-20 | — | — | US | claimed |