Histamine

Histamine

SCHEMBL9863744

CCOCC.Cl.NCCc1c[nH]cn1

nearest known ligand 0.40

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

HRH1

The experimentally established mechanism targets of Histamine. 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
HRH1 known ✓ P35367 4/20 0.34
TDP1 Q9NUW8 2/20 0.40
HRH4 Q9H3N8 5/20 0.37
HRH3 Q9Y5N1 4/20 0.37
TSHR P16473 2/20 0.37
CYP2C9 P11712 1/20 0.37
CYP2C19 P33261 1/20 0.37
MTOR P42345 1/20 0.37
HRH2 P25021 3/20 0.34
APEX1 P27695 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.34
LMNA P02545 1/20 0.32
MIF P14174 1/20 0.32
HTR2A P28223 1/20 0.30
HTR2C P28335 1/20 0.30
HTR2B P41595 1/20 0.30

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
Histamine SCHEMBL11002055 1.00 TDP1 (0.40) TDP1HRH4HRH3TSHRCYP2C9
Histamine SCHEMBL437541 0.98 HRH4 (0.38) TDP1HRH4HRH3TSHRCYP2C9
Histamine SCHEMBL58710 0.87 TDP1 (0.44) TDP1HRH4HRH3TSHRCYP2C9
Histamine SCHEMBL584026 0.87 TDP1 (0.44) TDP1HRH4HRH3TSHRCYP2C9
Histamine SCHEMBL887606 0.87
Histamine SCHEMBL10947437 0.85 HRH4 (0.41) TDP1HRH4HRH3TSHRCYP2C9
Histamine SCHEMBL9753206 0.85 HRH4 (0.44) TDP1HRH4HRH3TSHRCYP2C9
Histamine SCHEMBL28347218 0.85 TDP1 (0.42) TDP1HRH4HRH3TSHRCYP2C9
Histamine SCHEMBL289072 0.85 HRH4 (0.42) TDP1HRH4HRH3TSHRCYP2C9
Histamine SCHEMBL7444650 0.85 HRH4 (0.42) TDP1HRH4HRH3TSHRCYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-55083727-A None JP disclosed
CN-107141234-B A kind of azo-bis-iso-dimethyl synthetic method 邢保林 2019-06-21 CN disclosed
CN-107141234-A A kind of azo-bis-iso-dimethyl synthetic method 邢保林 2017-09-08 CN disclosed
CN-101309984-B Ink composition, manufacturing method of ink, ink set, and recording method FUJI PHOTO FILM CO LTD 2012-03-28 CN disclosed
CN-1997715-B Black ink composition, ink set containing the same, and ink jet recording method FUJI PHOTO FILM CO LTD 2011-01-05 CN disclosed
CN-101309984-A Ink composition, manufacturing method of ink, ink set, and recording method FUJIFILM CORP (JP) 2008-11-19 CN disclosed
CN-1997715-A Black ink composition, ink set containing the same, and ink jet recording method FUJI PHOTO FILM CO LTD (JP) 2007-07-11 CN disclosed
CN-1134148-A Antithrombotic amidinophenylalanine and amidinopyridylalanine derivs PFIZER RES & DEV (IE) 1996-10-23 CN disclosed
US-5047548-A 3-aryl-3-hydroxy-4-(1H-1,2,4-triazol-1-yl)butyramide and derivatives as antifungal agents PFIZER INC. (US) 1991-09-10 US disclosed
EP-0193191-B1 PYRIMIDINE DERIVATIVE AND LIQUID CRYSTAL COMPOSITION CONTAINING SAME Chisso Corporation (JP) 1989-09-13 EP disclosed
EP-0123907-B1 FLUOROPYRIMIDINE DERIVATIVES Chisso Corporation (JP) 1989-07-26 EP disclosed
US-4684476-A LOW VOLTAGE CHISSO CORPORATION (JP) 1987-08-04 US disclosed
EP-0193191-A2 Pyrimidine derivative and liquid crystal composition containing same Chisso Corporation (JP) 1986-09-03 EP disclosed
US-4581155-A LIQUID CRYSTALS CHISSO CORPORATION (JP) 1986-04-08 US disclosed
US-4503063-A PLANTS AND ANIMALS PFIZER INC. (US) 1985-03-05 US disclosed
EP-0123907-A2 Fluoropyrimidine derivatives Chisso Corporation (JP) 1984-11-07 EP disclosed
JP-S5583727-A PURIFICATION OF ORTHO ESTER NIPPON SYNTHETIC CHEM IND CO LTD:THE 1980-06-24 JP disclosed
US-3962242-A BACTERIOSTATS, URINARY TRACT INFECTIONS BOEHRINGER MANNHEIM G.M.B.H. (DT) 1976-06-08 US disclosed