Carbon Tetrachloride

Carbon Tetrachloride

SCHEMBL7586209

CO.ClC(Cl)(Cl)Cl.ClC(Cl)Cl.O

nearest known ligand 0.36

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO

The experimentally established mechanism targets of Carbon Tetrachloride. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 5)

geneUniProtsupporting neighboursconfidence
THRB known ✓ P10828 1/20 0.31
LMNA P02545 3/20 0.36
TSHR P16473 3/20 0.36
ALDH1A1 P00352 2/20 0.36
CYP2E1 P05181 1/20 0.36

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
Carbon Tetrachloride SCHEMBL8402265 0.95 TSHR (0.40) LMNATSHRALDH1A1CYP2E1THRB
Chloroform SCHEMBL28063298 0.85 LMNA (0.50) LMNATSHRALDH1A1
Chloroform SCHEMBL27706310 0.85 LMNA (0.50) LMNATSHRALDH1A1
Carbon Tetrachloride SCHEMBL27838684 0.85 LMNA (0.50) LMNATSHRALDH1A1CYP2E1
Chloroform SCHEMBL9617984 0.85 LMNA (0.50) LMNATSHRALDH1A1
Chloroform SCHEMBL25447 0.85
Carbon Tetrachloride SCHEMBL27802885 0.85
Chloroform SCHEMBL28040546 0.85
Chloroform SCHEMBL8907442 0.85 LMNA (0.50) LMNATSHRALDH1A1
Chloroform SCHEMBL28176439 0.85

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102093325-B The preparation method of a kind of high purity dinatin and herba lycopi flavone SHANGHAI TAUTO BIOTECH CO., LTD. (CN) 2015-08-05 CN claimed
CN-102093325-A Method for preparing high-purity hispidulin and herba lycopi flavone SHANGHAI TAUTO BIOTECH CO LTD 2011-06-15 CN claimed
CN-102093325-B The preparation method of a kind of high purity dinatin and herba lycopi flavone SHANGHAI TAUTO BIOTECH CO., LTD. (CN) 2015-08-05 CN disclosed
CN-102093325-A Method for preparing high-purity hispidulin and herba lycopi flavone SHANGHAI TAUTO BIOTECH CO LTD 2011-06-15 CN disclosed
EP-0923594-B1 BROMOTIACUMICIN COMPOUNDS ABBOTT LAB (US) 2002-10-02 EP disclosed
US-5767096-A PRODUCED BY CULTURING DACTYLOSPORANGIUM IN A BROMIDE ENRICHED NUTRIENT MEDIUM ABBOTT LABORATORIES (US) 1998-06-16 US disclosed
US-4780416-A BACTERICIDES, ANTITUMOR AGENTS BRISTOL-MYERS COMPANY (US) 1988-10-25 US disclosed
US-4631256-A FROM ACTINOMYCIN-ANTIBIOTIC, ANTITUMOR AGENT BRISTOL-MYERS COMPANY (US) 1986-12-23 US disclosed
US-4451456-A Antitumor antibacterial agents BRISTOL-MYERS COMPANY (US) 1984-05-29 US disclosed
US-4360458-A PEPTIDE ANTIBIOTICS, ANTIBIOTIC BBM-928 BRISTOL-MYERS COMPANY (US) 1982-11-23 US disclosed
US-3981862-A Preparation of C22-alkyl derivative of digoxin BOEHRINGER MANNHEIM G.M.B.H. (DT) 1976-09-21 US disclosed
US-3947404-A CARDIAC THERAPY BOEHRINGER MANNHEIM GMBH (DT) 1976-03-30 US disclosed