Chlorotriphenylmethane

Chlorotriphenylmethane

SCHEMBL28247644

C1CCNCC1.Cl.ClC(c1ccccc1)(c1ccccc1)c1ccccc1

nearest known ligand 0.41

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Chlorotriphenylmethane. 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
HRH1 known ✓ P35367 1/20 0.40
SCN1A known ✓ P35498 1/20 0.40
SCN2A known ✓ Q99250 1/20 0.40
SCN3A known ✓ Q9NY46 1/20 0.40
CHRM2 known ✓ P08172 2/20 0.37
CHRM4 known ✓ P08173 2/20 0.37
CHRM5 known ✓ P08912 2/20 0.37
CHRM1 known ✓ P11229 2/20 0.37
CHRM3 known ✓ P20309 2/20 0.37
SIGMAR1 known ✓ Q99720 3/20 0.34
OPRM1 known ✓ P35372 1/20 0.33
HTR3E known ✓ A5X5Y0 1/20 0.33
HTR3B known ✓ O95264 1/20 0.33
ADRB1 known ✓ P08588 1/20 0.33
HTR3A known ✓ P46098 1/20 0.33
HTR3D known ✓ Q70Z44 1/20 0.33
HTR3C known ✓ Q8WXA8 1/20 0.33
HTR2C known ✓ P28335 1/20 0.33
TSHR P16473 1/20 0.41
CYP2D6 P10635 2/20 0.40

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
Chlorotriphenylmethane SCHEMBL28051494 0.77 TSHR (0.58) TSHRALDH1A1CYP1A2MAPK1
Chlorotriphenylmethane SCHEMBL461 0.76 TSHR (0.65) TSHRALDH1A1CYP1A2MAPK1CYP2C19
Chlorotriphenylmethane SCHEMBL16781670 0.76 TSHR (0.65) TSHRALDH1A1CYP1A2MAPK1CYP2C19
Piperidine SCHEMBL28823404 0.75 KCNN4 (0.41) CYP2D6LMNAMEN1HRH1SCN1A
Chlorotriphenylmethane SCHEMBL28170744 0.74 TSHR (0.55) TSHRALDH1A1CYP1A2MAPK1
Chlorotriphenylmethane SCHEMBL11237663 0.74 TSHR (0.61) TSHRALDH1A1CYP1A2MAPK1CYP2C19
Chlorotriphenylmethane SCHEMBL113884 0.74 TSHR (0.61) TSHRALDH1A1CYP1A2MAPK1CYP2C19
Chlorotriphenylmethane SCHEMBL7567317 0.74 TSHR (0.61) TSHRALDH1A1CYP1A2MAPK1CYP2C19
Chlorotriphenylmethane SCHEMBL29446246 0.74 TSHR (0.61) TSHRALDH1A1CYP1A2MAPK1CYP2C19
Chlorotriphenylmethane SCHEMBL7246540 0.74 TSHR (0.61) TSHRALDH1A1CYP1A2MAPK1CYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108715605-A A kind of chemical synthesis process of antibacterial cyclic peptides Thermoactinoamide A 安徽工程大学 2018-10-30 CN disclosed