Histamine

Histamine

SCHEMBL16778301

Cl.Cl.NCCc1cnc[nH]1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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 14)

geneUniProtsupporting neighboursconfidence
HRH1 known ✓ P35367 8/20 0.95
HRH3 Q9Y5N1 7/20 1.00
HRH4 Q9H3N8 6/20 1.00
HRH2 P25021 4/20 1.00
APEX1 P27695 1/20 1.00
SMN1; SMN2 Q16637 1/20 1.00
LMNA P02545 2/20 0.95
MIF P14174 1/20 0.95
TSHR P16473 1/20 0.95
KDM4E B2RXH2 1/20 0.56
POLB P06746 1/20 0.56
RECQL P46063 1/20 0.56
PMP22 Q01453 1/20 0.56
NPSR1 Q6W5P4 1/20 0.56

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 SCHEMBL17377087 1.00
Histamine SCHEMBL288432 0.98
Histamine SCHEMBL15532340 0.93 HRH3 (0.91) HRH3HRH4HRH2APEX1SMN1; SMN2
Homohistamine SCHEMBL9799515 0.87 HRH3 (0.96) HRH3HRH4HRH2APEX1SMN1; SMN2
Histamine SCHEMBL123245 0.86 HRH3 (0.78) HRH3HRH4HRH2APEX1SMN1; SMN2
Histamine SCHEMBL27939119 0.85 HRH3 (0.75) HRH3HRH4HRH2APEX1SMN1; SMN2
Homohistamine SCHEMBL2092691 0.84
SCHEMBL8963903 0.83 HRH3 (0.73) HRH3HRH4HRH2APEX1SMN1; SMN2
Imbutamine SCHEMBL28015739 0.83 HRH3 (1.00) HRH3HRH4HRH2APEX1SMN1; SMN2
Histamine SCHEMBL3960364 0.82 HRH3 (0.70) HRH3HRH4HRH2APEX1SMN1; SMN2

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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4340838-A1 ORALLY ADMINISTERED COMPOSITIONS FOR CANCER TREATMENT Paz, Alberto (US) 2024-03-27 EP disclosed
EP-4320143-A1 METHODS FOR INHIBITING RAS The General Hospital Corporation (US) 2024-02-14 EP disclosed
WO-2022245650-A1 ORALLY ADMINISTERED COMPOSITIONS FOR CANCER TREATMENT PAZ ALBERTO (US) 2022-11-24 WO disclosed
US-11464217-B2 Rodents having genetically modified sodium channels and methods of use thereof REGENERON PHARMACEUTICALS, INC. (US) 2022-10-11 US disclosed
WO-2022212894-A1 METHODS FOR INHIBITING RAS THE GENERAL HOSPITAL CORPORATION (US) 2022-10-06 WO disclosed
CN-109790162-B Covalent inhibitors of PAD4 帕德罗科治疗公司 2022-06-28 CN disclosed
US-11352369-B2 Pyridine and pyrimidine derivatives ASTRAZENECA AB (SE) 2022-06-07 US disclosed
EP-3927153-A1 RODENTS HAVING GENETICALLY MODIFIED SODIUM CHANNELS AND METHODS OF USE THEREOF REGENERON PHARMACEUTICALS, INC. (US) 2021-12-29 EP disclosed
US-20210171541-A1 CHEMICAL COMPOUNDS ASTRAZENECA AB (SE) 2021-06-10 US disclosed
EP-3490989-B1 COVALENT INHIBITORS OF PAD4 PADLOCK THERAPEUTICS INC (US) 2020-09-09 EP disclosed
US-10703741-B2 Covalent inhibitors of PAD4 PADLOCK THERAPEUTICS, INC. (US) 2020-07-07 US disclosed
US-20190276432-A1 COVALENT INHIBITORS OF PAD4 PADLOCK THERAPEUTICS INC (US) 2019-09-12 US disclosed
CN-110049773-A TGF β antibody, method and purposes 供石公司 2019-07-23 CN disclosed
CN-108430491-A Peptide HOX治疗有限公司 2018-08-21 CN disclosed
CN-105492438-B Sulfomimine substituted 5-fluoro-N- (pyridin-2-yl) pyridin-2-amine derivatives and their use as CDK9 kinase inhibitors 拜耳医药股份有限公司 2018-08-07 CN disclosed
CN-105288647-B The preparation method of functionalization albumin and its nanometer formulation 中国药科大学 2018-05-25 CN disclosed
CN-107207475-A Fluorination benzofuranyl pyrimidine derivatives containing sulfone group 拜耳医药股份有限公司 2017-09-26 CN disclosed
US-9527852-B2 Phenyl-urea and phenyl-carbamate derivatives as inhibitors of protein aggregation NEUROPORE THERAPIES, INC. (US) 2016-12-27 US disclosed
US-9487524-B2 2016-11-08 US disclosed
US-20150166543-A1 PHENYL-UREA AND PHENYL-CARBAMATE DERIVATIVES AS INHIBITORS OF PROTEIN AGGREGATION UCB BIOPHARMA SPRL (BE) 2015-06-18 US 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 (5 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-20210171541-A1 CHEMICAL COMPOUNDS CDK9, BCL9, BCL9L HRH1 3814/4885HRH3 1863/4885HRH4 3441/4885
US-20150166543-A1 PHENYL-UREA AND PHENYL-CARBAMATE DERIVATIVES AS INHIBITORS OF PROTEIN AGGREGATION PARK7, PRNP, MAPT HRH1 3959/4885HRH3 3335/4885HRH4 4031/4885
US-10703741-B2 Covalent inhibitors of PAD4 PADI4, PADI1, PADI6 HRH1 3417/4885HRH3 2515/4885HRH4 2514/4885
US-11352369-B2 Pyridine and pyrimidine derivatives CDK9, BCL9, CDK19 HRH1 3411/4885HRH3 1189/4885HRH4 2645/4885
US-20190276432-A1 COVALENT INHIBITORS OF PAD4 PADI4, PADI1, PADI6 HRH1 3417/4885HRH3 2515/4885HRH4 2514/4885

“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.