Phenol

Phenol

SCHEMBL2853834

Cl.Cl.Cl.Cl.Oc1ccccc1

nearest known ligand 0.92

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 Phenol. 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
CA2 known ✓ P00918 4/20 0.92
GLA known ✓ P06280 1/20 0.92
ESR1 known ✓ P03372 9/20 0.50
ESR2 known ✓ Q92731 9/20 0.50
EGFR known ✓ P00533 1/20 0.47
PIK3CA known ✓ P42336 1/20 0.47
CA12 O43570 4/20 0.92
CA14 Q9ULX7 4/20 0.92
CA9 Q16790 3/20 0.92
CA3 P07451 3/20 0.92
CA4 P22748 3/20 0.92
CA1 P00915 2/20 0.92
TDP1 Q9NUW8 2/20 0.92
MMP3 P08254 1/20 0.59
BCL2L1 Q07817 1/20 0.59
ALDH1A1 P00352 4/20 0.54
CYP3A4 P08684 4/20 0.54
NPC1 O15118 3/20 0.54
LMNA P02545 3/20 0.54
CA5A P35218 3/20 0.54

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
Phenol SCHEMBL9303600 1.00 CA12 (0.92) CA12CA2CA14CA9CA3
Phenol SCHEMBL11851402 1.00 CA12 (0.92) CA12CA2CA14CA9CA3
Phenol SCHEMBL29015903 1.00 CA12 (0.92) CA12CA2CA14CA9CA3
Phenol SCHEMBL11236894 1.00 CA12 (0.92) CA12CA2CA14CA9CA3
Phenol SCHEMBL11176869 1.00 CA12 (0.92) CA12CA2CA14CA9CA3
Phenol SCHEMBL11467571 1.00 CA12 (0.92) CA12CA2CA14CA9CA3
Phenol SCHEMBL2861707 1.00
Phenol SCHEMBL31519853 1.00 CA12 (0.92) CA12CA2CA14CA9CA3
Phenol SCHEMBL909758 1.00
Phenol SCHEMBL28240446 1.00 CA12 (0.92) CA12CA2CA14CA9CA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102603471-A Production method of p-trifluoromethyl chlorobenzene NANTONG DONGCHANG CHEMICAL IND CO LTD 2012-07-25 CN claimed
CN-101947468-B Composite catalyst and application ZHEJIANG KANGFENG CHEMICALS CO LTD 2012-06-06 CN claimed
CN-101947468-A Composite catalyst and application ZHEJIANG KANGFENG CHEMICALS CO LTD 2011-01-19 CN claimed
US-12103926-B2 Compounds for treating huntington's disease PTC THERAPEUTICS, INC. (US) 2024-10-01 US disclosed
CN-107417490-A Tower continuous Light chlorimation legal system benzyl chloride 上海方纶新材料科技有限公司 2017-12-01 CN disclosed
CN-103936550-A Preparation method of 3,4,5-trichlorobenzotrifluoride JIANGSU FENGHUA CHEMICAL IND CO LTD 2014-07-23 CN disclosed
CN-102603471-A Production method of p-trifluoromethyl chlorobenzene NANTONG DONGCHANG CHEMICAL IND CO LTD 2012-07-25 CN disclosed
CN-101947468-B Composite catalyst and application ZHEJIANG KANGFENG CHEMICALS CO LTD 2012-06-06 CN disclosed
CN-101947468-A Composite catalyst and application ZHEJIANG KANGFENG CHEMICALS CO LTD 2011-01-19 CN disclosed
EP-1443890-B1 OXIDATION COLOURING AGENT BASED ON BICYCLIC DEVELOPER COMPONENTS HENKEL AG & CO KGAA (DE) 2010-01-13 EP disclosed
EP-1443888-A2 OXIDATION COLOURING AGENT WITH BIS (5-AMINO-2-HYDROXYPHENYL)-METHANE Henkel Kommanditgesellschaft auf Aktien (DE) 2004-08-11 EP disclosed
WO-2003041671-A2 OXIDATION COLOURING AGENT WITH BIS (5-AMINO-2-HYDROXYPHENYL)-METHANE AND/OR 4-AMINO-2-{(4-[5'-AMINO-2'-HYDROXY-PHENYL)-METHYL-] PIPERAZINYL)-METHYL}-PHENOL TETRAHYDROCHLORIDE HENKEL KOMMANDITGESELLSCHAFT AUF AKTIEN (DE) 2003-05-22 WO disclosed
US-3978262-A METHOD OF SIZING TEXTILE FIBERS USING WATER-SOLUBLE SULFONATED POLYESTERS AND PRODUCTS SO MADE RHONE-PROGIL (FR) 1976-08-31 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 (1 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-12103926-B2 Compounds for treating huntington's disease HTT, HYPK, FH CA2 3500/4885GLA 84/4885ESR1 4574/4885

“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.