Cellobiose

Cellobiose

SCHEMBL1308532

O.OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O.OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O

nearest known ligand 0.67

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Cellobiose. 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
▸ MEN1 known ✓ O00255 2/20 0.54
▸ PTGS1 known ✓ P23219 1/20 0.46
▸ PDE4A known ✓ P27815 1/20 0.46
▸ PDE3A known ✓ Q14432 1/20 0.46
▸ LGALS8 O00214 1/20 0.59
▸ LGALS3 P17931 1/20 0.59
▸ LGALS4 P56470 1/20 0.59
▸ KMT2A Q03164 2/20 0.54
▸ AMY2A P04746 3/20 0.53
▸ TYR P14679 2/20 0.49
▸ AMY1A P0DUB6 2/20 0.49
▸ GJA1 P17302 1/20 0.48
▸ GJB2 P29033 1/20 0.48
▸ CYP2C9 P11712 1/20 0.48
▸ TSHR P16473 1/20 0.48
▸ ALDH1A1 P00352 1/20 0.48
▸ IGF2R P11717 1/20 0.47
▸ GAA P10253 2/20 0.46
▸ MGAM O43451 2/20 0.46
▸ MAPT P10636 1/20 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
Maltotriose SCHEMBL2377340 1.00 LGALS8 (0.59) LGALS8LGALS3LGALS4MEN1KMT2A
Cellobiose SCHEMBL16786 1.00 LGALS8 (0.59) LGALS8LGALS3LGALS4MEN1KMT2A
Cellobiose SCHEMBL373436 1.00 LGALS8 (0.59) LGALS8LGALS3LGALS4MEN1KMT2A
Cellobiose SCHEMBL2229473 1.00 LGALS8 (0.59) LGALS8LGALS3LGALS4MEN1KMT2A
Water SCHEMBL466158 1.00 LGALS8 (0.59) LGALS8LGALS3LGALS4MEN1KMT2A
Cellobiose SCHEMBL19582547 1.00 LGALS8 (0.59) LGALS8LGALS3LGALS4MEN1KMT2A
Cellobiose SCHEMBL373437 1.00 LGALS8 (0.59) LGALS8LGALS3LGALS4MEN1KMT2A
Cellobiose SCHEMBL373528 1.00 LGALS8 (0.59) LGALS8LGALS3LGALS4MEN1KMT2A
Cellobiose SCHEMBL7072560 1.00 LGALS8 (0.59) LGALS8LGALS3LGALS4MEN1KMT2A
Maltose SCHEMBL230121 1.00 LGALS8 (0.59) LGALS8LGALS3LGALS4MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1233969-B2 DISACCHARIDE DERIVATIVES PROTHERICS MEDICINES DEV LTD (GB) 2016-12-14 — — EP disclosed
US-8637659-B2 Mono-and disaccharide derivatives PROTHERICS MEDICINES DEVELOPMENT LIMITED (GB) 2014-01-28 — — US disclosed
CN-103127143-A Inhalation drug composition with budesonide and nitric oxide synthase (NOS) inhibitor TIANJIN JINYAO GROUP CO LTD 2013-06-05 — — CN disclosed
CN-103127141-A Inhalation drug composition with mometasone furoate and nitric oxide synthase (NOS) inhibitor TIANJIN JINYAO GROUP CO LTD 2013-06-05 — — CN disclosed
CN-103127144-A Inhalation drug composition with ciclesonide and nitric oxide synthase (NOS) inhibitor TIANJIN JINYAO GROUP CO LTD 2013-06-05 — — CN disclosed
CN-103127133-A Inhalation drug composition with fluticasone propionate and nitric oxide synthase (NOS) inhibitor TIANJIN JINYAO GROUP CO LTD 2013-06-05 — — CN disclosed
US-20120288528-A1 MONO-AND DISACCHARIDE DERIVATIVES BTG INTERNATIONAL LIMITED (GB) 2012-11-15 — — US disclosed
CN-101108250-B Mono- and disaccharide derivatives PROTHERICS MEDICINES DEV LTD 2012-01-11 — — CN disclosed
US-20110305730-A1 MONO-AND DISACCHARIDE DERIVATIVES HILGERS LUCAS ALFONSUS T (NL) 2011-12-15 — — US disclosed
US-8052981-B2 Mono- and disaccharide derivatives PROTHERICS MEDICINES DEVELOPMENT LIMITED (GB) 2011-11-08 — — US disclosed
US-20090304723-A1 Mono-and disaccharide derivatives BTG INTERNATIONAL LIMITED (GB) 2009-12-10 — — US disclosed
EP-1233969-B1 MONO- AND DISACCHARIDE DERIVATIVES COVACCINE B V (NL) 2008-03-05 — — EP disclosed
CN-101108250-A Mono- and disaccharide derivatives COVACCINE B V (NL) 2008-01-23 — — CN disclosed
CN-100345592-C Mono-and disaccharide derivatives COVACCINE B V (NL) 2007-10-31 — — CN disclosed
US-20050256060-A1 Mono-and disaccharide derivatives COVACCINE B.V. 2005-11-17 — — US disclosed
CN-1433423-A Mono-and disaccharide derivatives COVACCINE B V (NL) 2003-07-30 — — CN disclosed
EP-1233969-A2 MONO- AND DISACCHARIDE DERIVATIVES Covaccine B.V. (NL) 2002-08-28 — — EP disclosed
WO-2001040240-A2 MONO- AND DISACCHARIDE DERIVATIVES COVACCINE B.V. (NL) 2001-06-07 — — WO disclosed
EP-1104767-A1 Mono- and disaccharide derivatives containing both fatty acid ester and sulfate ester groups Stichting Dienst Landbouwkundig Onderzoek (NL) 2001-06-06 — — EP disclosed
Send feedback