SCHEMBL2453699

SCHEMBL2453699

COc1ccc(CCCO)cc1OC.CS(=O)(=O)O

nearest known ligand 0.57

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
POLB P06746 2/20 0.57
KDM4E B2RXH2 2/20 0.57
CA12 O43570 2/20 0.56
CA1 P00915 2/20 0.56
CA2 P00918 2/20 0.56
CA9 Q16790 2/20 0.56
CA5A P35218 1/20 0.56
CA14 Q9ULX7 1/20 0.56
SMN1; SMN2 Q16637 1/20 0.56
ATM Q13315 2/20 0.53
TNKS2 Q9H2K2 1/20 0.51
MAPT P10636 1/20 0.51
HTT P42858 2/20 0.51
ALDH1A1 P00352 1/20 0.50
KMT2A Q03164 1/20 0.50
GAA P10253 1/20 0.49

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
SCHEMBL81112 0.90 KDM4E (0.63) POLBKDM4ECA2ATMTNKS2
Alcohol SCHEMBL15062546 0.87 KDM4E (0.59) POLBKDM4ECA2ATMTNKS2
SCHEMBL4860600 0.85 KDM4E (0.61) POLBKDM4ECA2ATMTNKS2
SCHEMBL7320148 0.85 LMNA (0.50) POLBKDM4ESMN1; SMN2MAPTALDH1A1
SCHEMBL9506664 0.83 KDM4E (0.59) POLBKDM4ECA2ATMTNKS2
SCHEMBL7184663 0.83 KDM4E (0.59) POLBKDM4ECA2ATMTNKS2
SCHEMBL2802611 0.83 KDM4E (0.59) POLBKDM4ECA2ATMTNKS2
SCHEMBL6572223 0.83 CA2 (0.54) POLBKDM4ECA12CA1CA2
SCHEMBL7156624 0.82 PLAAT3 (0.56) POLBKDM4ECA12CA1CA2
SCHEMBL10415400 0.81 CA2 (0.52) POLBKDM4ECA12CA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8017646-B2 e.g. 1-{3-[3-(3,4-dimethoxyphenyl)propoxy]propyl}pyrrolidine; neurodegenerative disorders, antidepressant, antidiabetic, hypotensive agent, cognition activator; BIOPROJET (FR) 2011-09-13 US disclosed
US-20080182876-A1 Histamine H3-Receptor Ligands and Their Therapeutic Application BIOPROJET (FR) 2008-07-31 US disclosed
EP-1874747-A1 HISTAMINE H3-RECEPT0R LIGANDS AND THEIR THERAPEUTIC APPLICATION BIOPROJET (FR) 2008-01-09 EP disclosed
WO-2006117611-A1 HISTAMINE H3-RECEPT0R LIGANDS AND THEIR THERAPEUTIC APPLICATION BIOPROJET (FR) 2006-11-09 WO disclosed
EP-1717233-A1 Histamine H3-receptor ligands and their therapeutic application BIOPROJET (FR) 2006-11-02 EP disclosed
US-5276060-A Methods of treating tumors with compositions of catecholic butanes BLOCK/CHEMEX, G.P. (US) 1994-01-04 US disclosed
EP-0288534-B1 COMPOSITIONS OF CATECHOLIC BUTANES WITH ZINC CHEMEX PHARMACEUTICALS, INC. (US) 1991-12-18 EP disclosed
US-5008294-A Topical administration CHEMEX PHARMACEUTICALS, INC. (US) 1991-04-16 US disclosed
EP-0290442-A4 PHARMACOLOGICALLY ACTIVE COMPOUNDS AND MIXTURES THEREOF, ORGANIC COMPOSITIONS AND METAL SALTS. CHEMEX PHARMACEUTICALS INC (US) 1990-07-03 EP disclosed
US-4880637-A ALCOHOLS, ETHERS OR ESTERS, AS ANTITUMOR AGENTS, SKIN DISORDERS CHEMEX PHARMACEUTICALS, INC. (US) 1989-11-14 US disclosed
EP-0288534-A4 COMPOSITIONS OF CATECHOLIC BUTANES WITH ZINC. CHEMEX PHARMACEUTICALS INC (US) 1989-02-23 EP disclosed
EP-0297733-A2 Pharmaceutical compositions comprising catecholic butanes BLOCK DRUG COMPANY, INC. (US) 1989-01-04 EP disclosed
EP-0290442-A1 PHARMACOLOGICALLY ACTIVE COMPOUNDS AND MIXTURES THEREOF, ORGANIC COMPOSITIONS AND METAL SALTS CHEMEX PHARMACEUTICALS, INC. (US) 1988-11-17 EP disclosed
EP-0288534-A1 COMPOSITIONS OF CATECHOLIC BUTANES WITH ZINC. CHEMEX PHARMACEUTICALS INC (US) 1988-11-02 EP disclosed
WO-1988003806-A1 PHARMACOLOGICALLY ACTIVE COMPOSITIONS OF CATECHOLIC BUTANES WITH ZINC CHEMEX PHARMACEUTICALS, INC. (US) 1988-06-02 WO disclosed
WO-1988003805-A1 PHARMACOLOGICALLY ACTIVE COMPOUNDS AND MIXTURES THEREOF, ORGANIC COMPOSITIONS AND METAL SALTS CHEMEX PHARMACEUTICALS, INC. (US) 1988-06-02 WO disclosed
WO-1988003026-A1 COMPOSITIONS OF CATECHOLIC BUTANES WITH ZINC CHEMEX PHARMACEUTICALS, INC. (US) 1988-05-05 WO 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-20080182876-A1 Histamine H3-Receptor Ligands and Their Therapeutic Application HRH3, HRH4, HRH1 POLB 4442/4885KDM4E 1619/4885CA12 1212/4885

“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.