SCHEMBL4368908

SCHEMBL4368908

C1=C(Cc2ccccc2)N=N[N]1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CALM1 P0DP23 1/20 0.46
▸ LMNA P02545 2/20 0.35
▸ PLA2G10 O15496 1/20 0.35
▸ PLA2G2A P14555 1/20 0.35
▸ BCL2 P10415 1/20 0.34
▸ BCL2L1 Q07817 1/20 0.34
▸ TAAR1 Q96RJ0 3/20 0.34
▸ ALDH1A1 P00352 3/20 0.34
▸ HRH3 Q9Y5N1 1/20 0.34
▸ CYP1A2 P05177 1/20 0.33
▸ ADRA2A P08913 1/20 0.33
▸ CYP2D6 P10635 1/20 0.33
▸ TSHR P16473 1/20 0.33
▸ ADRA2B P18089 1/20 0.33
▸ ADRA2C P18825 1/20 0.33
▸ ADRA1D P25100 1/20 0.33
▸ ADRA1A P35348 1/20 0.33
▸ ADRA1B P35368 1/20 0.33
▸ RAB9A P51151 1/20 0.33
▸ SMN1; SMN2 Q16637 1/20 0.33

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
SCHEMBL15094393 0.70 CALM1 (0.46) CALM1LMNABCL2BCL2L1TAAR1
SCHEMBL19100321 0.69 KCNH2 (0.46) LMNAALDH1A1CYP1A2TSHRRAB9A
SCHEMBL8655842 0.67 CALM1 (0.38) CALM1LMNATAAR1ALDH1A1HRH3
Diphenylmethane SCHEMBL14763944 0.66 CALM1 (1.00) CALM1LMNAPLA2G10PLA2G2ABCL2
Diphenylmethane SCHEMBL28172316 0.66 CALM1 (1.00) CALM1LMNAPLA2G10PLA2G2ABCL2
Diphenylmethane SCHEMBL1303 0.66 CALM1 (1.00) CALM1LMNAPLA2G10PLA2G2ABCL2
Diphenylmethane SCHEMBL4361124 0.66 CALM1 (1.00) CALM1LMNAPLA2G10PLA2G2ABCL2
Diphenylmethane SCHEMBL3792579 0.66 CALM1 (1.00) CALM1LMNAPLA2G10PLA2G2ABCL2
SCHEMBL8650674 0.65 CALM1 (0.46) CALM1LMNABCL2BCL2L1TAAR1
SCHEMBL8610753 0.64 CALM1 (0.44) CALM1LMNABCL2BCL2L1TAAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2009012375-A2 SQUARATE KINASE INHIBITORS WYETH (US) 2009-01-22 — — WO claimed
EP-1637525-A1 Benzoxazole compound, process for producing the same, and herbicides Ube Industries, Ltd. (JP) 2006-03-22 — — EP claimed
US-20050233909-A1 Benzoxazole compounds, process for producing the same and herbicides UBE INDUSTRIES, LTD. (JP) 2005-10-20 — — US claimed
US-20040014977-A1 Benzoxazole compound, process for producing the same, and herbicide KYOYU AGRI CO., LTD. (JP) 2004-01-22 — — US claimed
CN-105131104-B The reconstruct and sugar conjugation of peptide 诺和诺德公司 2018-11-16 — — CN disclosed
CN-103384661-B Mineralocorticoid receptor antagonists 默沙东公司 2016-08-10 — — CN disclosed
CN-105131104-A Remodeling and glycoconjugation of peptides NOVO NORDISK AS 2015-12-09 — — CN disclosed
CN-103384661-A Mineralocorticoid receptor antagonists MERCK SHARP & DOHME 2013-11-06 — — CN disclosed
CN-1635901-B Methods for reconstitution and glycoconjugation of peptides NEOSE TECHNOLOGIES INC 2012-03-28 — — CN disclosed
CN-102180944-A Remodeling and glycoconjugation of peptides NEOSE TECHNOLOGIES INC 2011-09-14 — — CN disclosed
CN-101724075-A Remodeling and glycoconjugation of peptides NEOSE TECHNOLOGIES INC 2010-06-09 — — CN disclosed
CN-100522988-C Glycopegylation methods and proteins/peptides produced by the methods NEOSE TECHNOLOGIES INC (DK) 2009-08-05 — — CN disclosed
US-20020040002-A1 Hydroxamic acids substituted by heterocycles useful for inhibition of tumor necrosis factor ZENECA LIMITED 2002-04-04 — — US disclosed
US-6242615-B1 AMIDATION OF ACID CONTAINING COMPOUNDS; USEFUL IN INHIBITING TUMOR NECROSIS FACTOR AND METALLOPROTEINASES ZENECA LIMITED (GB) 2001-06-05 — — US disclosed
EP-0971881-A1 PROCESS FOR THE PREPARATION OF N-(3-HYDROXY-SUCCINYL)-AMINO ACID DERIVATIVES AstraZeneca AB (SE) 2000-01-19 — — EP disclosed
WO-1998043946-A1 PROCESS FOR THE PREPARATION OF N-(3-HYDROXY-SUCCINYL)-AMINO ACID DERIVATIVES ZENECA LIMITED (GB) 1998-10-08 — — WO disclosed
EP-0866367-A2 Radiation sensitive composition JSR Corporation (JP) 1998-09-23 — — EP disclosed
US-5652233-A CARBAPENICILLINS ZENECA LIMITED (GB) 1997-07-29 — — US disclosed
US-5527791-A Carbapenem antibiotic compounds ZENECA LIMITED (GB) 1996-06-18 — — US disclosed
US-5478820-A Carbapenem deivatives; bactericides ZENECA LTD. (GB) 1995-12-26 — — 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 (3 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-20020040002-A1 Hydroxamic acids substituted by heterocycles useful for inhibition of tumor necrosis factor MMP1, HCAR1, MMP13 CALM1 3328/4885LMNA 1557/4885PLA2G10 2444/4885
US-20050233909-A1 Benzoxazole compounds, process for producing the same and herbicides CBR3, CBR1, CYP4X1 CALM1 796/4885LMNA 3101/4885PLA2G10 4829/4885
US-20040014977-A1 Benzoxazole compound, process for producing the same, and herbicide CBR1, CBR3, CYP4X1 CALM1 1649/4885LMNA 2248/4885PLA2G10 4849/4885

“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.

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