Result for 012A17BDF91DFB3F7AC781CE8B033682ED8FBB46

Query result

Key Value
FileName./usr/share/doc/rdkit/html/api/rdkit.ML.Neural.ActFuncs.ActFunc-class.html
FileSize7132
MD5A7E744DE0DEBF67C2176E3A0DFD49093
SHA-1012A17BDF91DFB3F7AC781CE8B033682ED8FBB46
SHA-256F8C667FB35F917EFDAAF5ECD982B4C1A81FCA82C5E34F447DC606D0BD52393DD
SSDEEP96:tGxRxHhdFd3hdS3dq/hdf3d2CQoNJjQWSmpPfAUhot6FIwTdBzQbH9SCMJvMX+SQ:tGxDHDX/3NhA1eap/x8HDX/3S8rwM9
TLSHT176E150009AE0636A846B90DFE3B05FCB9EE284ABC7020454F96DA7761FC9F49452787D
hashlookup:parent-total3
hashlookup:trust65

Network graph view

Parents (Total: 3)

The searched file hash is included in 3 parent files which include package known and seen by metalookup. A sample is included below:

Key Value
FileSize3371876
MD5D0918ED1E48F5743752EF5ED2A2E5497
PackageDescriptionCollection of cheminformatics and machine-learning software RDKit is a Python/C++ based cheminformatics and machine-learning software environment. Features Include: . * Chemical reaction handling and transforms * Substructure searching with SMARTS * Canonical SMILES * Molecule-molecule alignment * Large number of molecular descriptors, including topological, compositional, EState, SlogP/SMR, VSA and Feature-map vectors * Fragmentation using RECAP rules * 2D coordinate generation and depiction, including constrained depiction * 3D coordinate generation using geometry embedding * UFF and MMFF94 forcefields * Chirality support, including calculation of (R/S) stereochemistry codes * 2D pharmacophore searching * Fingerprinting, including Daylight-like, atom pairs, topological torsions, Morgan alogrithm and MACCS keys * Calculation of shape similarity * Multi-molecule maximum common substructure * Machine-learning via clustering and information theory algorithms * Gasteiger-Marsili partial charge calculation . File formats RDKit supports include MDL Mol, PDB, SDF, TDT, SMILES and RDKit binary format.
PackageMaintainerUbuntu Developers <ubuntu-devel-discuss@lists.ubuntu.com>
PackageNamepython-rdkit
PackageSectionpython
PackageVersion201603.5+dfsg-1ubuntu1
SHA-15AC2BE0014E36C9522CD94D6583CA42036FF3ABE
SHA-256DFECA2C05A81A0AB5965DF1083AD9FA7FA156A16A1508DE0A4EDB5B71B3981D3
Key Value
FileSize3407012
MD54C015FBBD6038FB6B77363E70039B974
PackageDescriptionCollection of cheminformatics and machine-learning software RDKit is a Python/C++ based cheminformatics and machine-learning software environment. Features Include: . * Chemical reaction handling and transforms * Substructure searching with SMARTS * Canonical SMILES * Molecule-molecule alignment * Large number of molecular descriptors, including topological, compositional, EState, SlogP/SMR, VSA and Feature-map vectors * Fragmentation using RECAP rules * 2D coordinate generation and depiction, including constrained depiction * 3D coordinate generation using geometry embedding * UFF and MMFF94 forcefields * Chirality support, including calculation of (R/S) stereochemistry codes * 2D pharmacophore searching * Fingerprinting, including Daylight-like, atom pairs, topological torsions, Morgan alogrithm and MACCS keys * Calculation of shape similarity * Multi-molecule maximum common substructure * Machine-learning via clustering and information theory algorithms * Gasteiger-Marsili partial charge calculation . File formats RDKit supports include MDL Mol, PDB, SDF, TDT, SMILES and RDKit binary format.
PackageMaintainerUbuntu Developers <ubuntu-devel-discuss@lists.ubuntu.com>
PackageNamepython-rdkit
PackageSectionpython
PackageVersion201603.5+dfsg-1ubuntu1
SHA-1B577F0E9059F73625561F21279DABF096248CD01
SHA-2565A9F71D50800BB849317F88DF5CA829FBA519546FE48B3653C30ABF5459D33E3
Key Value
FileSize5445688
MD5C685A367407880E9993C0A2F0E6E7D9D
PackageDescriptionCollection of cheminformatics and machine-learning software (documentation) RDKit is a Python/C++ based cheminformatics and machine-learning software environment. . This package contains the documentation.
PackageMaintainerUbuntu Developers <ubuntu-devel-discuss@lists.ubuntu.com>
PackageNamerdkit-doc
PackageSectiondoc
PackageVersion201603.5+dfsg-1ubuntu1
SHA-11CA767E4DEB3F13ABF6EB79BC3BAB0AFAE4F66A0
SHA-25635761085B9C2755F03FEFADA0CA43C2BD635481B4E9444057CBFE7C815EE0AEC