Diphenylamine

Diphenylamine

SCHEMBL1361625

Cl.O=CCC=O.c1ccc(Nc2ccccc2)cc1

nearest known ligand 0.60

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 Diphenylamine. 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
PTGS1 known ✓ P23219 1/20 0.57
SLC6A2 known ✓ P23975 1/20 0.57
PTGS2 known ✓ P35354 1/20 0.57
HTR2B known ✓ P41595 1/20 0.57
MAPK14 known ✓ Q16539 1/20 0.45
GAA known ✓ P10253 3/20 0.44
HSD17B10 Q99714 5/20 0.60
ALDH1A1 P00352 8/20 0.57
ALOX12 P18054 4/20 0.57
L3MBTL1 Q9Y468 4/20 0.57
TSHR P16473 4/20 0.57
TDP1 Q9NUW8 4/20 0.57
ALOX15 P16050 2/20 0.57
MAPK1 P28482 1/20 0.57
MAPT P10636 8/20 0.50
MEN1 O00255 3/20 0.50
KMT2A Q03164 3/20 0.50
AR P10275 1/20 0.50
CYP3A4 P08684 5/20 0.46
HTT P42858 2/20 0.46

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
Diphenylamine SCHEMBL28045270 0.97 HSD17B10 (0.63) HSD17B10ALDH1A1ALOX12L3MBTL1TSHR
Diphenylamine SCHEMBL27805382 0.84 HSD17B10 (0.52) HSD17B10ALDH1A1ALOX12L3MBTL1TSHR
Diphenylamine SCHEMBL27541752 0.83 HSD17B10 (0.46) HSD17B10ALDH1A1ALOX12L3MBTL1TSHR
Diphenylamine SCHEMBL27671183 0.83 HSD17B10 (0.57) HSD17B10ALDH1A1ALOX12L3MBTL1TSHR
Diphenylamine SCHEMBL192934 0.81 HSD17B10 (0.92) HSD17B10ALDH1A1ALOX12L3MBTL1TSHR
Diphenylamine SCHEMBL11684039 0.81 HSD17B10 (0.92) HSD17B10ALDH1A1ALOX12L3MBTL1TSHR
SCHEMBL6608023 0.79 ALDH1A1 (0.56) HSD17B10ALDH1A1ALOX12L3MBTL1TSHR
Diphenylamine SCHEMBL7230087 0.79 HSD17B10 (0.67) HSD17B10ALDH1A1ALOX12L3MBTL1TSHR
Diphenylamine SCHEMBL21145018 0.79 HSD17B10 (0.67) HSD17B10ALDH1A1ALOX12L3MBTL1TSHR
Diphenylamine SCHEMBL11650896 0.78 HSD17B10 (0.86) HSD17B10ALDH1A1ALOX12L3MBTL1TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117487373-A Synthesis method of cyanine dye 宁夏医科大学 2024-02-02 CN claimed
CN-116715976-A Chiral carbon-containing pentamethine cyanine dye, and preparation method and application thereof 大连理工大学 2023-09-08 CN claimed
CN-115925667-A Ratio type near-infrared fluorescent probe molecule and preparation method and application thereof 复旦大学 2023-04-07 CN claimed
CN-113337138-B Indole cyanine dye 天津全和诚科技有限责任公司 2022-08-09 CN claimed
CN-112409590-B Organic nano assembly for biological imaging of second window in near infrared region and preparation method and application thereof 复旦大学 2021-10-26 CN claimed
CN-112225721-B Acid-responsive near-infrared lysosome organic small-molecule fluorescent probe and preparation method and application thereof 复旦大学 2021-09-17 CN claimed
CN-113337138-A Novel indole cyanine dye 天津全和诚科技有限责任公司 2021-09-03 CN claimed
CN-112409590-A Organic nano assembly for biological imaging of second window in near infrared region and preparation method and application thereof 复旦大学 2021-02-26 CN claimed
CN-112225721-A Acid-responsive near-infrared lysosome organic small-molecule fluorescent probe and preparation method and application thereof 复旦大学 2021-01-15 CN claimed
CN-110396304-A Cyanine dyestuff and preparation method thereof UNIV SHENZHEN 2019-11-01 CN claimed
CN-108504130-A A kind of colored cyanine fluorochrome and its synthetic method 湖南大学 2018-09-07 CN claimed
CN-118324776-A BRD4 small molecule fluorescent probe and preparation method and application thereof 山东第一医科大学(山东省医学科学院) 2024-07-12 CN disclosed
CN-113490660-B Compounds of formula (I) 住友化学株式会社 2024-07-09 CN disclosed
CN-113490661-B Compounds of formula (I) 住友化学株式会社 2024-02-13 CN disclosed
CN-117487373-A Synthesis method of cyanine dye 宁夏医科大学 2024-02-02 CN disclosed
CN-104704366-B Azaindole quinoline-the cyanine dye and its bioconjugates of hydroxamic acid substitution 贝克顿·迪金森公司 2018-06-19 CN disclosed
CN-106459001-A Polymethine compounds and their use as fluorescent labels 伊鲁米纳剑桥有限公司 2017-02-22 CN disclosed
US-20160263249-A1 NEAR-INFRARED FLUORESCENT CONTRAST BIOIMAGING AGENTS AND METHODS OF USE THEREOF BETH ISRAEL DEACONESS MEDICAL CENTER (US) 2016-09-15 US disclosed
US-8067602-B2 Asymmetric cyanine fluorescent dyes, compositions and their use in staining biological samples SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (CN) 2011-11-29 US disclosed
US-20090176270-A1 ASYMMETRIC CYANINE FLUORESCENT DYES, COMPOSITIONS AND THEIR USE IN STAINING BIOLOGICAL SAMPLES SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (CN) 2009-07-09 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-20160263249-A1 NEAR-INFRARED FLUORESCENT CONTRAST BIOIMAGING AGENTS AND METHODS OF USE THEREOF CD68, MSR1, CD47 PTGS1 755/4885SLC6A2 3124/4885PTGS2 766/4885
US-20090176270-A1 ASYMMETRIC CYANINE FLUORESCENT DYES, COMPOSITIONS AND THEIR USE IN STAINING BIOLOGICAL SAMPLES IK, CRY1, CRY2 PTGS1 4589/4885SLC6A2 4029/4885PTGS2 4688/4885

“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.