Hydrazinecarboxamide

Hydrazinecarboxamide

SCHEMBL825388

NNC(N)=O.NNC(N)=O.O=S(=O)(O)O

nearest known ligand 0.71

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

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
MAOA known ✓ P21397 1/20 0.71
MAOB known ✓ P27338 1/20 0.71
TSHR P16473 3/20 0.71
NFKB1 P19838 2/20 0.71
CYP1A2 P05177 1/20 0.71
THPO P40225 1/20 0.71
LMNA P02545 4/20 0.67
KDM4E B2RXH2 4/20 0.44
BLM P54132 3/20 0.44
CA5A P35218 3/20 0.43
CA5B Q9Y2D0 2/20 0.43
CA2 P00918 4/20 0.41
CA9 Q16790 4/20 0.41
CYP3A4 P08684 1/20 0.41
PMP22 Q01453 1/20 0.41
ALDH1A1 P00352 3/20 0.38
CA1 P00915 3/20 0.38
NT5E P21589 1/20 0.38
CA4 P22748 1/20 0.38
CA6 P23280 1/20 0.38

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 SCHEMBL7615707 1.00 TSHR (0.71) TSHRNFKB1CYP1A2MAOAMAOB
Hydrazinecarboxamide SCHEMBL28328714 0.97 LMNA (0.73) TSHRNFKB1CYP1A2MAOAMAOB
Hydrazinecarboxamide SCHEMBL9797148 0.97 LMNA (0.73) TSHRNFKB1CYP1A2MAOAMAOB
Hydrazinecarboxamide SCHEMBL9051248 0.91 LMNA (0.65) TSHRNFKB1CYP1A2MAOAMAOB
Hydrazinecarboxamide SCHEMBL5345890 0.90 TSHR (0.67) TSHRNFKB1CYP1A2MAOAMAOB
Hydrazinecarboxamide SCHEMBL11526612 0.88 TSHR (0.56) TSHRNFKB1CYP1A2MAOAMAOB
Hydrazinecarboxamide SCHEMBL27857386 0.87 TSHR (0.62) TSHRNFKB1CYP1A2MAOAMAOB
Hydrazinecarboxamide SCHEMBL27857387 0.87 TSHR (0.62) TSHRNFKB1CYP1A2MAOAMAOB
Hydrazinecarboxamide SCHEMBL18613867 0.84 TSHR (1.00) TSHRNFKB1CYP1A2MAOAMAOB
Hydrazinecarboxamide SCHEMBL15393 0.84

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026099772-A1 POTASSIUM SULFATE - UREA AMMONIUM SULFATE FERTILIZERS AND METHODS FOR PRODUCING AND USING THE SAME SABIC Agri-Nutrients Company (SA) 2026-05-15 WO claimed
EP-4161874-B1 METHOD TO PRODUCE A UREA AMMONIUM SULPHATE-BASED COMPOSITION YARA INT ASA (NO) 2026-03-11 EP claimed
EP-4706394-A2 USE OF ALKOXYPYRAZOLES AS NITRIFICATION INHIBITORS BASF SE (DE) 2026-03-11 EP claimed
US-12559442-B2 Use of N-functionalized alkoxy pyrazole compounds as nitrification inhibitors BASF SE (DE) 2026-02-24 US claimed
EP-3758492-B1 USE OF ALKOXYPYRAZOLES AS NITRIFICATION INHIBITORS BASF SE (DE) 2026-01-28 EP claimed
EP-3294690-B1 USE OF PROPARGYL THIOETHER COMPOUNDS AS NITRIFICATION INHIBITORS BASF SE (DE) 2026-01-21 EP claimed
EP-3790852-B1 IMPROVED UREA-BASED BLEND COMPOSITION AND METHOD FOR THE MANUFACTURE THEREOF YARA INT ASA (NO) 2025-12-03 EP claimed
US-12484580-B2 Use of alkoxypyrazoles as nitrification inhibitors BASF SE (DE) 2025-12-02 US claimed
EP-4441014-B1 BENZOTHIAZOLE DERIVATIVE AS A UREASE INHIBITOR FOR FERTILIZER APPLICATION SABIC AGRI NUTRIENTS COMPANY (SA) 2025-11-26 EP claimed
EP-4613726-A1 PRODUCTION OF NITROGEN, POTASSIUM, SULFUR NUTRIENT THROUGH DE-CARBONIZATION AND UTILIZATION OF CALCIUM SULFATE Sabic Agri-Nutrients Company (SA) 2025-09-10 EP claimed
WO-2007147209-A1 HERB ICIDAL COMPOSITION CONTAINING AMITROLE AND METHOD FOR CONTROLLING WEEDS NUFARM AUSTRALIA LIMITED (AU) 2007-12-27 WO claimed
EP-1861335-A1 PIPE REACTOR AND PLANT FOR MANUFACTURING OF ESPECIALLY UREA AMMONIUM SULPHATE YARA International ASA (NO) 2007-12-05 EP claimed
CN-101006011-A Production method of fertilizer containing urea and ammonium sulfate YARA INT ASA (NO) 2007-07-25 CN claimed
EP-1781569-A1 METHOD FOR PRODUCING A FERTILIZER CONTAINING UREA AND AMMONIUM SULPHATE YARA International ASA (NO) 2007-05-09 EP claimed
WO-2006093413-A1 PIPE REACTOR AND PLANT FOR MANUFACTURING OF ESPECIALLY UREA AMMONIUM SULPHATE YARA INTERNATIONAL ASA (NO) 2006-09-08 WO claimed
WO-2006004424-A1 METHOD FOR PRODUCING A FERTILIZER CONTAINING UREA AND AMMONIUM SULPHATE YARA INTERNATIONAL ASA (NO) 2006-01-12 WO claimed
CN-1297426-A Granulation method of urea contg. fertilizer AIRBORNE IND MINERALS INC (CA) 2001-05-30 CN claimed
US-6179893-B1 CONTROLLING RATIOS, PARTICLE SIZES; FLUIDIZES BED GRANULATION TOYO ENGINEERING CORPORATION (JP) 2001-01-30 US claimed
WO-1995001943-A1 METHOD FOR INCREASING CROP YIELD RIZZO JOHN M (US) 1995-01-19 WO claimed
US-5330552-A Method for increasing crop yield RIZZO JOHN M (US) 1994-07-19 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 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-12559442-B2 Use of N-functionalized alkoxy pyrazole compounds as nitrification inhibitors NAT1, CBR1, CBR3 MAOA 80/4885MAOB 39/4885TSHR 399/4885
US-12484580-B2 Use of alkoxypyrazoles as nitrification inhibitors CYP1B1, NOS1, CYP1A2 MAOA 140/4885MAOB 108/4885TSHR 4130/4885

“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.