Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Dimethylamine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | MMP1 known ✓ | P03956 | 1/20 | 0.39 |
| ▸ | GAA known ✓ | P10253 | 1/20 | 0.35 |
| ▸ | ACHE known ✓ | P22303 | 1/20 | 0.32 |
| ▸ | MMP2 | P08253 | 1/20 | 0.39 |
| ▸ | MMP3 | P08254 | 1/20 | 0.39 |
| ▸ | MMP9 | P14780 | 1/20 | 0.39 |
| ▸ | EPHX1 | P07099 | 4/20 | 0.38 |
| ▸ | PAOX | Q6QHF9 | 1/20 | 0.36 |
| ▸ | MCL1 | Q07820 | 1/20 | 0.36 |
| ▸ | MAPT | P10636 | 2/20 | 0.35 |
| ▸ | NPC1 | O15118 | 1/20 | 0.35 |
| ▸ | RAB9A | P51151 | 1/20 | 0.35 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.35 |
| ▸ | TGFBR1 | P36897 | 1/20 | 0.34 |
| ▸ | KDM4C | Q9H3R0 | 1/20 | 0.34 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.32 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.32 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.32 |
| ▸ | NPSR1 | Q6W5P4 | 1/20 | 0.32 |
| ▸ | PLA2G2A | P14555 | 1/20 | 0.32 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Dimethylamine SCHEMBL10790993 | 1.00 | MMP1 (0.39) | MMP1MMP2MMP3MMP9EPHX1 | |
| Dimethylamine SCHEMBL42843 | 0.98 | MMP1 (0.40) | MMP1MMP2MMP3MMP9EPHX1 | |
| Dimethylamine SCHEMBL8509082 | 0.96 | MMP1 (0.39) | MMP1MMP2MMP3MMP9EPHX1 | |
| Dimethylamine SCHEMBL8511788 | 0.96 | MMP1 (0.39) | MMP1MMP2MMP3MMP9EPHX1 | |
| Hydrochloric Acid SCHEMBL3148805 | 0.96 | MMP1 (0.41) | MMP1MMP2MMP3MMP9EPHX1 | |
| Dimethylamine SCHEMBL15902173 | 0.94 | MMP1 (0.38) | MMP1MMP2MMP3MMP9EPHX1 | |
| Hydrochloric Acid SCHEMBL28010702 | 0.93 | MMP1 (0.40) | MMP1MMP2MMP3MMP9EPHX1 | |
| SCHEMBL149370 | 0.93 | — | — | |
| Dimethylamine SCHEMBL9572414 | 0.92 | MMP1 (0.36) | MMP1MMP2MMP3MMP9EPHX1 | |
| Methylamine SCHEMBL6561969 | 0.91 | MMP1 (0.39) | MMP1MMP2MMP3MMP9EPHX1 |
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 8 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-10337282-B2 | Methods and compositions for reducing water production in fractures or voids in subterranean formations | HALLIBURTON ENERGY SERVICES, INC. (US) | 2019-07-02 | — | — | US | disclosed |
| US-20180022982-A1 | METHODS AND COMPOSITIONS FOR REDUCING WATER PRODUCTION IN FRACTURES OR VOIDS IN SUBTERRANEAN FORMATIONS | HALLIBURTON ENERGY SERVICES, INC. (US) | 2018-01-25 | — | — | US | disclosed |
| WO-2016153519-A1 | METHODS AND COMPOSITIONS FOR REDUCING WATER PRODUCTION IN FRACTURES OR VOIDS IN SUBTERRANEAN FORMATIONS | HALLIBURTON ENERGY SERVICES, INC. (US) | 2016-09-29 | — | — | WO | disclosed |
| US-8991495-B2 | Methods for protecting a hydrocarbon-producing zone of a subterranean formation using a relative permeability modifier | HALLIBURTON ENERGY SERVICES, INC. (US) | 2015-03-31 | — | — | US | disclosed |
| WO-2013173600-A2 | METHODS FOR PROTECTING A HYDROCARBON-PRODUCING ZONE OF A SUBTERRANEAN FORMATION USING A RELATIVE PERMEABILITY MODIFIER | HALLIBURTON ENERGY SERVICES, INC. (US) | 2013-11-21 | — | — | WO | disclosed |
| US-20130306314-A1 | Methods for Protecting a Hydrocarbon-Producing Zone of a Subterranean Formation Using a Relative Permeability Modifier | HALLIBURTON ENERGY SERVICES, INC. (US) | 2013-11-21 | — | — | US | disclosed |
| US-8470746-B2 | Methods relating to the stabilization of hydrophobically modified hydrophilic polymer treatment fluids under alkaline conditions | HALLIBURTON ENERGY SERVICES, INC. (US) | 2013-06-25 | — | — | US | disclosed |
| US-20120135895-A1 | Compositions and Methods Relating to the Stabilization of Hydrophobically Modified Hydrophilic Polymer Treatment Fluids Under Alkaline Conditions | HALLIBURTON ENERGY SERVICES, INC. (US) | 2012-05-31 | — | — | US | disclosed |