Hydrazinecarboxamide

Hydrazinecarboxamide

SCHEMBL5345890

CS(=O)(=O)O.NNC(N)=O

nearest known ligand 0.67

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of Hydrazinecarboxamide. 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
MAOB known ✓ P27338 1/20 0.67
TSHR P16473 3/20 0.67
NFKB1 P19838 2/20 0.67
CYP1A2 P05177 1/20 0.67
MAOA P21397 1/20 0.67
THPO P40225 1/20 0.67
LMNA P02545 5/20 0.62
BLM P54132 4/20 0.39
CA2 P00918 3/20 0.39
CA5A P35218 3/20 0.39
PMP22 Q01453 2/20 0.39
CA9 Q16790 2/20 0.39
CYP3A4 P08684 2/20 0.39
CRBN Q96SW2 1/20 0.38
KDM4E B2RXH2 5/20 0.36
ALDH1A1 P00352 3/20 0.36
CA1 P00915 2/20 0.35
CA5B Q9Y2D0 2/20 0.35
NT5E P21589 1/20 0.35
CA4 P22748 1/20 0.35

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
Hydrazinecarboxamide SCHEMBL825388 0.90 TSHR (0.71) TSHRNFKB1CYP1A2MAOAMAOB
Hydrazinecarboxamide SCHEMBL7615707 0.90 TSHR (0.71) TSHRNFKB1CYP1A2MAOAMAOB
Hydrazinecarboxamide SCHEMBL9797148 0.87 LMNA (0.73) TSHRNFKB1CYP1A2MAOAMAOB
Hydrazinecarboxamide SCHEMBL28328714 0.87 LMNA (0.73) TSHRNFKB1CYP1A2MAOAMAOB
Hydrazinecarboxamide SCHEMBL27857387 0.84 TSHR (0.62) TSHRNFKB1CYP1A2MAOAMAOB
Hydrazinecarboxamide SCHEMBL27857386 0.84 TSHR (0.62) TSHRNFKB1CYP1A2MAOAMAOB
Urea SCHEMBL2959932 0.82
Hydrazinecarboxamide SCHEMBL5075202 0.82 TSHR (0.83) TSHRNFKB1CYP1A2MAOAMAOB
Urea SCHEMBL28006959 0.82 LMNA (0.50) TSHRNFKB1CYP1A2MAOAMAOB
Hydrazinecarboxamide SCHEMBL18613867 0.82 TSHR (1.00) TSHRNFKB1CYP1A2MAOAMAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7235671-B2 Process for preparing 3-chloromethyl-1,2,4-triazolin-5-one MERCK & CO. INC. (US) 2007-06-26 US disclosed
US-20060052355-A1 reacting a chloro contaiing triaryl- or trialkyl-orthoester with a sulfonic acid salt of semicarbazide in an organic solvent, adding a brine solution to the concentrated reaction mixture,cooling the mixture to form a solid product, acidification with aqueous acid MERCK SHARP & DOHME CORP. 2006-03-09 US disclosed
EP-1549623-A4 PROCESS FOR PREPARING 3-CHLOROMETHYL-1,2,4-TRIAZOLIN-5-ONE MERCK & CO INC (US) 2005-10-05 EP disclosed
EP-1549623-A2 PROCESS FOR PREPARING 3-CHLOROMETHYL-1,2,4-TRIAZOLIN-5-ONE Merck & Co., Inc. (US) 2005-07-06 EP disclosed
WO-2004017898-A2 PROCESS FOR PREPARING 3-CHLOROMETHYL-1,2,4-TRIAZOLIN-5-ONE MERCK & CO., INC. (US) 2004-03-04 WO disclosed
EP-0789570-A4 ORAL HYPOGLYCEMIC AGENTS LILLY CO ELI (US) 1998-09-30 EP disclosed
EP-0789570-A1 ORAL HYPOGLYCEMIC AGENTS ELI LILLY AND COMPANY (US) 1997-08-20 EP disclosed
US-5641796-A PHENYL-OXAZOLYL-ALKYLOXY OR THIO-PHENYLALKYL TRIAZOLINE-3-ONE OR THIONE ANTIDIABETIC AGENT ELI LILLY AND COMPANY (US) 1997-06-24 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 (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-20060052355-A1 reacting a chloro contaiing triaryl- or trialkyl-orthoester with a sulfonic acid salt of semicarbazide in an organic solvent, adding a brine solution to the concentrated reaction mixture,cooling the mixture to form a solid product, acidification with aqueous acid CLIC1, CTRC, NISCH MAOB 554/4885TSHR 967/4885NFKB1 2444/4885

“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.