Tryptophol

Tryptophol

SCHEMBL649225

CS(=O)(=O)O.OCCc1c[nH]c2ccccc12

nearest known ligand 0.61

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of Tryptophol. 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
HTR2A known ✓ P28223 4/20 0.58
HTR1A known ✓ P08908 2/20 0.58
HTR2C known ✓ P28335 2/20 0.54
HTR1D known ✓ P28221 1/20 0.54
HTR1B known ✓ P28222 1/20 0.54
CYP1A2 P05177 2/20 0.58
MEN1 O00255 1/20 0.58
LMNA P02545 1/20 0.58
PKM P14618 1/20 0.58
TSHR P16473 1/20 0.58
CYP2C19 P33261 1/20 0.58
BLM P54132 1/20 0.58
KMT2A Q03164 1/20 0.58
ALDH1A1 P00352 2/20 0.58
KDM4E B2RXH2 1/20 0.58
HTT P42858 1/20 0.58
CYP19A1 P11511 2/20 0.56
GAA P10253 1/20 0.55
MAPT P10636 1/20 0.55
MPO P05164 1/20 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
Tryptophol SCHEMBL29364545 0.88 HTR2A (0.67) CYP1A2MEN1LMNAPKMTSHR
Tryptophol SCHEMBL196126 0.88 HTR2A (0.67) CYP1A2MEN1LMNAPKMTSHR
Tryptophol SCHEMBL15619233 0.87 HTR2A (0.61) CYP1A2MEN1LMNAPKMTSHR
Tryptamine SCHEMBL9321966 0.86 HTR2A (0.76) CYP1A2MEN1LMNAPKMTSHR
Tryptophol SCHEMBL21682597 0.86 MEN1 (0.64) CYP1A2MEN1LMNAPKMTSHR
SCHEMBL1272559 0.81 HTR2A (0.57) CYP1A2MEN1LMNAPKMTSHR
SCHEMBL30952641 0.81 HTR2A (0.57) CYP1A2MEN1LMNAPKMTSHR
Indolylpropionic Acid SCHEMBL195854 0.80 MAPT (0.61) CYP1A2MEN1LMNAPKMTSHR
SCHEMBL760892 0.80 CYP19A1 (0.70) CYP1A2MEN1LMNAPKMTSHR
Tryptamine SCHEMBL27538374 0.79 HTR2C (0.81) CYP1A2MEN1LMNAPKMTSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101370804-B Novel aminophenyl derivatives as histone deacetylase inhibitors JANSSEN PHARMACEUTICA NV 2013-05-29 CN disclosed
US-8119650-B2 Aminophenyl derivatives as novel inhibitors of histone deacetylase JANSSEN PHARMACEUTICA N.V. (BG) 2012-02-21 US disclosed
CN-1993353-B Substituted indolyl alkylamino derivatives as novel inhibitors of histone deacetylase JANSSEN PHARMACEUTICA NV 2010-12-01 CN disclosed
EP-1981874-B1 AMINOPHENYL DERIVATIVES AS NOVEL INHIBITORS OF HISTONE DEACETYLASE JANSSEN PHARMACEUTICA NV (BE) 2009-05-27 EP disclosed
CN-101370804-A Novel aminophenyl derivatives as histone deacetylase inhibitors JANSSEN PHARMACEUTICA NV (BE) 2009-02-18 CN disclosed
US-20090018152-A1 Aminophenyl Derivatives as Novel Inhibitors of Histone Deacetylase JANSSEN PHARMACEUTICA N.V. (BE) 2009-01-15 US disclosed
EP-1981874-A1 AMINOPHENYL DERIVATIVES AS NOVEL INHIBITORS OF HISTONE DEACETYLASE Janssen Pharmaceutica, N.V. (BE) 2008-10-22 EP disclosed
WO-2007082878-A1 AMINOPHENYL DERIVATIVES AS NOVEL INHIBITORS OF HISTONE DEACETYLASE JANSSEN PHARMACEUTICA N.V. (BE) 2007-07-26 WO disclosed
CN-1993353-A Substituted indolyl alkylamino derivatives as novel inhibitors of histone deacetylase JANSSEN PHARMACEUTICA NV (BE) 2007-07-04 CN 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-20090018152-A1 Aminophenyl Derivatives as Novel Inhibitors of Histone Deacetylase HDAC1, HDAC9, HDAC11 HTR2A 2727/4885HTR1A 1796/4885HTR2C 3676/4885

“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.