3,4,5-Trihydroxybenzohydrazide structure
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Common Name | 3,4,5-Trihydroxybenzohydrazide | ||
|---|---|---|---|---|
| CAS Number | 5782-85-4 | Molecular Weight | 184.14900 | |
| Density | 1.64g/cm3 | Boiling Point | N/A | |
| Molecular Formula | C7H8N2O4 | Melting Point | 295-298ºC | |
| MSDS | N/A | Flash Point | N/A | |
| Name | 3,4,5-Trihydroxybenzhydrazide |
|---|---|
| Synonym | More Synonyms |
| Density | 1.64g/cm3 |
|---|---|
| Melting Point | 295-298ºC |
| Molecular Formula | C7H8N2O4 |
| Molecular Weight | 184.14900 |
| Exact Mass | 184.04800 |
| PSA | 115.81000 |
| LogP | 0.49810 |
| Index of Refraction | 1.721 |
| InChIKey | FBCVSPDPLQWYJV-UHFFFAOYSA-N |
| SMILES | NNC(=O)c1cc(O)c(O)c(O)c1 |
| HS Code | 2928000090 |
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~57%
3,4,5-Trihydrox... CAS#:5782-85-4 |
| Literature: Khaledi, Hamid; Alhadi, Abeer A.; Yehye, Wagee A.; Ali, Hapipah Mohd; Abdulla, Mahmood A.; Hassandarvish, Pouya Archiv der Pharmazie, 2011 , vol. 344, # 11 p. 703 - 709 |
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~%
3,4,5-Trihydrox... CAS#:5782-85-4 |
| Literature: Chem. Zentralbl., , vol. 75, # II p. 1494 |
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3,4,5-Trihydrox... CAS#:5782-85-4 |
| Literature: Oriental Journal of Chemistry, , vol. 27, # 4 p. 1437 - 1442 |
| Precursor 4 | |
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| DownStream 0 | |
| HS Code | 2928000090 |
|---|---|
| Summary | 2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0% |
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Name: Primary cell-based high-throughput screening assay for identification of compounds th...
Source: Johns Hopkins Ion Channel Center
Target: regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id: JHICC_RGS_Act_HTS
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Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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Name: uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
Source: Burnham Center for Chemical Genomics
Target: N/A
External Id: BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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|
Name: High throughput fluorescence intensity-based biochemical assay to screen for small mo...
Source: University of Pittsburgh Molecular Library Screening Center
Target: furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id: MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
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Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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Name: Flow Cytometric HTS Screen for inhibitors of the ABC transporter ABCB6 for Validation...
Source: NMMLSC
Target: ATP-binding cassette sub-family B member 6, mitochondrial [Homo sapiens]
External Id: UNMCMD_ABCB6_1o_ValidationSet
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Name: Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
Source: Broad Institute
Target: N/A
External Id: 7124-01_Inhibitor_SinglePoint_HTS_Activity
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| 3,4,5-trihydroxybenzohydrazide |