Benzylhydrazine

Benzylhydrazine

SCHEMBL55982

Cl.Cl.NNCc1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Benzylhydrazine. 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 2/20 0.54
HTR1A known ✓ P08908 1/20 0.54
ADRA2A known ✓ P08913 1/20 0.54
PTGS1 known ✓ P23219 1/20 0.54
SLC6A2 known ✓ P23975 1/20 0.54
MAOB known ✓ P27338 1/20 0.54
ADRA1A known ✓ P35348 1/20 0.54
CA2 known ✓ P00918 3/20 0.50
GAA known ✓ P10253 2/20 0.50
CYP3A4 P08684 4/20 1.00
MAPT P10636 4/20 1.00
IDO1 P14902 3/20 0.94
KDM4E B2RXH2 2/20 0.56
LMNA P02545 2/20 0.56
KMT2A Q03164 2/20 0.56
BLM P54132 1/20 0.56
PMP22 Q01453 1/20 0.56
CYP1A2 P05177 2/20 0.54
NFKB1 P19838 2/20 0.54
ALDH1A1 P00352 2/20 0.54

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
Benzylhydrazine SCHEMBL176887 1.00 CYP3A4 (1.00) CYP3A4MAPTIDO1KDM4ELMNA
Benzylhydrazine SCHEMBL29080870 0.97 CYP3A4 (0.95) CYP3A4MAPTIDO1KDM4ELMNA
Benzylhydrazine SCHEMBL28071597 0.97 CYP3A4 (0.95) CYP3A4MAPTIDO1KDM4ELMNA
Benzylhydrazine SCHEMBL176979 0.97
Benzylhydrazine SCHEMBL8861708 0.94 IDO1 (0.94) CYP3A4MAPTIDO1KDM4ELMNA
Benzylhydrazine SCHEMBL28389744 0.94 IDO1 (0.94) CYP3A4MAPTIDO1KDM4ELMNA
Benzylhydrazine SCHEMBL27509884 0.94 IDO1 (0.94) CYP3A4MAPTIDO1KDM4ELMNA
Benzylhydrazine SCHEMBL10436051 0.94 IDO1 (0.94) CYP3A4MAPTIDO1KDM4ELMNA
Benzylhydrazine SCHEMBL27529745 0.94 IDO1 (0.94) CYP3A4MAPTIDO1KDM4ELMNA
Benzylhydrazine SCHEMBL697342 0.92 IDO1 (0.90) CYP3A4MAPTIDO1KDM4ELMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025020685-A1 PEROVSKITE THIN FILM LAYER AND PREPARATION METHOD THEREFOR, AND PEROVSKITE SILICON STACKED SOLAR CELL AND PREPARATION METHOD THEREFOR 通威太阳能(成都)有限公司 2025-01-30 WO claimed
CN-117042571-A Perovskite film additive, perovskite solar cell and preparation method of perovskite film additive 上海乐天钙钛光电科技有限公司 2023-11-10 CN claimed
CN-116887609-A Perovskite thin film layer and preparation method thereof, perovskite silicon laminated solar cell and preparation method thereof 通威太阳能(成都)有限公司 2023-10-13 CN claimed
US-10329264-B2 Process for the preparation of isocarboxazid LUNDBECK PHARMACEUTICALS ITALY S.P.A. (IT) 2019-06-25 US claimed
EP-3328842-B1 PROCESS FOR THE PREPARATION OF ISOCARBOXAZID LUNDBECK PHARMACEUTICALS ITALY S P A (IT) 2019-06-12 EP claimed
US-20180215722-A1 PROCESS FOR THE PREPARATION OF ISOCARBOXAZID LUNDBECK PHARMACEUTICALS ITALY S.P.A. (IT) 2018-08-02 US claimed
EP-3328842-A1 PROCESS FOR THE PREPARATION OF ISOCARBOXAZID Lundbeck Pharmaceuticals Italy S.p.A. (IT) 2018-06-06 EP claimed
WO-2017021246-A1 PROCESS FOR THE PREPARATION OF ISOCARBOXAZID LUNDBECK PHARMACEUTICALS ITALY S.P.A. (IT) 2017-02-09 WO claimed
CN-102617472-A Preparation method of tetra-substituted olefin and pyrazole derivative thereof DALIAN CHEMICAL PHYSICS INST 2012-08-01 CN claimed
EP-0918052-B1 Improved polymeric mdi color BAYER AG (US) 2003-05-28 EP claimed
US-5942151-A PREVENTING THE DISCOLORATION OF PRODUCING POLYMETHYLENEPOLYPHENYLENE POLYISOCYANATE BY ADDING AN ADDITIVE HYDRAZINE OR A HYDRAZINE DERIVATIVE BAYER CORPORATION (US) 1999-08-24 US claimed
EP-0918052-A1 Improved polymeric mdi color Bayer Corporation (US) 1999-05-26 EP claimed
EP-3762377-B1 PYRIDINONE- AND PYRIDAZINONE-BASED COMPOUNDS AND MEDICAL USES THEREOF UNIV CORNELL (US) 2025-08-20 EP disclosed
EP-4598923-A1 SUPRAMOLECULAR POLYMER THERAPEUTICS AND DIAGNOSTICS The Regents of the University of California (US) 2025-08-13 EP disclosed
US-12371432-B2 Haloallylamine compounds and application thereof TRANSTHERA SCIENCES (NANJING), INC. (CN) 2025-07-29 US disclosed
EP-3728194-B1 QUINOLINE SULFONAMIDE COMPOUNDS AND THEIR USE AS ANTIBACTERIAL AGENTS OTAGO INNOVATION LTD (NZ) 2025-06-04 EP disclosed
US-4041046-A INTERMEDIATES FOR THE CORRESPONDING HERBICIDAL PYRAZOLIUM SALTS ON AMERICAN CYANAMID COMPANY (US) 1977-08-09 US disclosed
US-4009277-A 1,2-Dialkyl-3,4,5-trisubstituted pyrazolium salts as fungicidal agents AMERICAN CYANAMID COMPANY (US) 1977-02-22 US disclosed
US-4000301-A Fungicidal use of 4-alkoxypyrazoles AMERICAN CYANAMID COMPANY (US) 1976-12-28 US disclosed
US-3963742-A 1,2-Dialkyl-3,4,5-trisubstituted pyrazolium salts as herbicidal agents AMERICAN CYANAMID COMPANY (US) 1976-06-15 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-12371432-B2 Haloallylamine compounds and application thereof ADRA1D, ADRA1A, VAPA MAOA 485/4885HTR1A 269/4885ADRA2A 22/4885
US-20180215722-A1 PROCESS FOR THE PREPARATION OF ISOCARBOXAZID IDH2, IDH1, IDH3A MAOA 978/4885HTR1A 3732/4885ADRA2A 2961/4885
US-10329264-B2 Process for the preparation of isocarboxazid IDH2, IDH1, IDH3A MAOA 978/4885HTR1A 3732/4885ADRA2A 2961/4885

“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.