Hydromorphone

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Hydromorphone

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Hydromorphone

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Hydromorphone

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Hydromorphone

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SMILES:CN1CCC23C4=C5C=CC(O)=C4OC2C(=O)CCC3C1C5

InChI:InChI=1S/C17H19NO3/c1-18-7-6-17-10-3-5-13(20)16(17)21-15-12(19)4-2-9(14(15)17)8-11(10)18/h2,4,10-11,16,19H,3,5-8H2,1H3

InChI key:WVLOADHCBXTIJK-UHFFFAOYSA-N

Sinónimos: DB00327,Hydromorphone 0.1 mg/ml in Methanol,BDBM50241341,Hydromorphone-D6,Idromorfone [DCIT],Hidromorfona [INN-Spanish], Dilaudid (TN), Idromorfone [DCIT],dilaudid,HYDROMORPHONE [HSDB],NSC 19046,Hydromorphone Form II,Hydromorphonum [INN-Latin], (5alpha)-3-hydroxy-17-methyl-4,5-epoxymorphinan-6-one,SCHEMBL2255,466-99-9, Hidromorfona, 4,5-Epoxy-3-hydroxy-17-methylmorphinan-6-one, 466-99-9, Morphinan-6-one, 4,5alpha-epoxy-3-hydroxy-17-methyl-(8CI),(4R,4aR,7aR,12bS)-9-hydroxy-3-methyl-1,2,4,4a,5,6,7a,13-octahydro-4,12-methanobenzofuro[3,2-e]isoquinoline-7-one,Hydromorfona,CHEBI:5790, Dilaudid-hp,GTPL7082,Dilaudid,4,5.alpha.-Epoxy-3-hydroxy-17-methylmorphinan-6-one,Morphinan-6-one, 4,5-epoxy-3-hydroxy-17-methyl-, (5.alpha.)-, Morphinone, dihydro-, Novolaudon, Hydromorfona, Dilaudid,Dihydromorphinone, Laudacon,6-Deoxy-7,8-dihydro-6-oxomorphine,Laudicon,Hydromorphone,Dihydromorfinon,Laudacon, DiMo, Palladone,Dilaudid Oros,UNII-Q812464R06,WLN: T B6566 B6/CO 4ABBC R BX FV HO PN GHT&&TTJ JQ P1,diluadid, Laudicon,D08047,Hydromorphone solution, 1 mg/mL in methanol, ampule of 1 mL, certified reference material,Morphinan-6-one,5-epoxy-3-hydroxy-17-methyl-, (5.alpha.)-,(4R,4aR,7aR,12bS)-9-Hydroxy-3-methyl-1,2,4,4a,5,6,7a,13-octahydro-4,12-methanobenzofuro[3,2-e]isoquinolin-7-one],Q303646,Hydromorphone 1.0 mg/ml in Methanol,DiMo, Hydromorphonum [INN-Latin],NSC-19046,Hydromorphon,HSDB 3341,(1S,5R,13R,17R)-10-hydroxy-4-methyl-12-oxa-4-azapentacyclo[9.6.1.0?,??.0?,??.0?,??]octadeca-7,9,11(18)-trien-14-one,(-)-Hydromorphone,Hydromorphone (INN),HYDROMORPHONE [MI], Dimorphone,Palladone, Hydromorfona [Spanish],Hydromorphone form I,(-)-(5R)-4,5-Epoxy-3-hydroxy-9alpha-methylmorphinan-6-one, (-)-(5R)-4,5-Epoxy-3-hydroxy-9alpha-methylmorphinan-6-one,Dihydromorfinon [Czech],4,5-Epoxy-3-hydroxy-17-methylmorphinan-6-one,4,5alpha-Epoxy-3-hydroxy-17-methyl-6-morphinanone,Dimorphone, Dihydromorfinon [Czech],HYDROMORPHONE [WHO-DD],Morphinan-6-one, 4,5alpha-epoxy-3-hydroxy-17-methyl-, Palladone SR (TN), Dihydromorfinon,hydromorphone, Hydromorphonum, DiMo,4,5alpha-Epoxy-3-hydroxy-17-methylmorphinan-6-one,EINECS 207-383-5,Morphinone, dihydro-,4,5-Epoxy-3-hydroxy-17-trideuteromethyl-15,15,16-trideuteromorphinan-6-one,Jurnista, Hydromorphone prodrug, Dilaudid Oros,HYDROMORPHONE [VANDF],Q812464R06,7,8-Dihydromorphinone,DTXSID8023133,ZINC402954,DEA No. 9150,Dilaudid-hp, Hydromorphone [INN:BAN],Morphinan-6-one, 4,5-epoxy-3-hydroxy-17-methyl-, (5alpha)-,(1S,5R,13R,17R)-10-hydroxy-4-methyl-12-oxa-4-azapentacyclo[9.6.1.0^{1,13}.0^{5,17}.0^{7,18}]octadeca-7(18),8,10-trien-14-one,Hidromorfona,IDS-NH-004,Hydromorfona [Spanish],NSC19046,Morphinan-6-one, 4,5-alpha-epoxy-3-hydroxy-17-methyl-,Morphinan-6-one,5.alpha.-epoxy-3-hydroxy-17-methyl-,3-hydroxy-17-methyl-4,5alpha-epoxymorphinan-6-one, Hidromorfona [INN-Spanish], Idromorfone,(4R,4aR,7aR,12bS)-9-hydroxy-3-methyl-1,2,4,4a,5,6,7a,13-octahydro-4,12-methanobenzofuro[3,2-e]isoquinolin-7-one, Dihydromorphinone,Hydromorphone [INN:BAN],N02AA03,Novolaudon, 6-Deoxy-7,8-dihydro-6-oxomorphine, Hydromorphon,HYDROCODONE HYDROGEN TARTRATE 2.5-HYDRATE IMPURITY K [EP IMPURITY], (-)-Hydromorphone, 4,5alpha-Epoxy-3-hydroxy-17-methyl-6-morphinanone,CHEMBL398707,Idromorfone, 7,8-Dihydromorphinone, Palladone (TN),(5alpha)-3-hydroxy-17-methyl-4,5-epoxymorphinan-6-one, 3-hydroxy-17-methyl-4,5alpha-epoxymorphinan-6-one, Hydromorphone (INN),HYDROMORPHONE [INN],C07042, Hydromorphone HCL,Hydromorphonum

Similitudes

Poder identificar moléculas similares a la que estudiamos puede permitir inferir algunas de sus propiedades. Hay varias formas de medir la similitud entre moléculas, por su estructura, efectos, interacciones farmacológicas, etc. A continuación, puedes encontrar moléculas similares según varios criterios y herramientas que desarrollamos. Para comprender las limitaciones de estas comparaciones, es crucial referirse siempre a la metodología utilizada para medir esas similitudes.Ten en cuenta: Esta información se proporciona únicamente con fines informativos y no debe interpretarse como asesoramiento médico.

Para medir la similitud estructural, utilizamos el método de Mol2vec Mol2Vec, que es una red neuronal que procesa moléculas y las transforma en puntos en el espacio, de modo que las moléculas con subestructuras químicamente relacionadas se transforman en puntos cercanos en el espacio.

Propiedades de la molécula

Utilizando el modelo de KGPT Aprendizaje Profundo, predecimos varias propiedades de la molécula. Las predicciones se agrupan según el conjunto de datos que se utilizó para obtener esas predicciones. Junto con cada predicción, proporcionamos un gráfico que muestra la distribución de los valores predichos en el conjunto de datos de entrenamiento/prueba/validación. Esto da una estimación de la confiabilidad del modelo.

Description: A dataset focused on predicting the inhibitory effects of molecules on the enzyme beta-secretase 1 (BACE1). BACE1 inhibition is a potential target for Alzheimer's disease treatment.
Class
TrainValTest
2.88-3.70-1.36
Description: A dataset providing insights on the ability of molecules to penetrate the blood-brain barrier. Crucial for understanding the potential of molecules as central nervous system drugs.
p_np
TrainValTest
-2.24-3.290.40
Description: This dataset deals with the FDA approval status and clinical trial toxicity of molecules. Important for understanding the safety and regulatory status of compounds.
CT_TOX
TrainValTest
-0.49-0.78-0.91
FDA_APPROVED
TrainValTest
0.53-1.27-0.50
Description: A dataset that predicts the solubility of molecules in water. Solubility is an essential property influencing bioavailability and the potential formulation of a drug.
logSolubilitylog(mol/L)
-0.50
TrainValTest
Description: This dataset is centered on predicting the free energy when a molecule is dissolved in water. The energy changes can affect molecular interactions in biological systems.
freesolvkcal/mol
-1.69
TrainValTest
Description: A dataset predicting the lipophilicity of molecules. Lipophilicity is a crucial factor affecting the distribution, metabolism, and excretion of drugs in the body.
lipoAlogP
-1.16
TrainValTest
Description: This dataset gives insights into the metabolic stability of molecules. High metabolic stability often results in a longer half-life, influencing drug dosage and frequency.
low
TrainValTest
-0.17-3.50-2.88
high
TrainValTest
0.72-3.55-0.49
27 entries
12 entries
617 entries

Perspectivas avanzadas

En lo siguiente, proporcionamos un análisis más avanzado sobre las interacciones de una molécula con el metabolismo humano, sitios de acoplamiento, etc.

Afinidades

Afinidades de unión con una lista de 61 sitios de acoplamiento predefinidos. Estas afinidades se utilizan para calcular las similitudes de interacciones.

Interacción de esta molécula con el metabolismo

Utilizamos un modelo de Aprendizaje Profundo para predecir las interacciones de esta molécula con el metabolismo. Consulta la fuente para entender la metodología.

Reacciones que metabolizan esta molécula
Aromatic OH-glucuronidation BTMR0166
Enzimas: 2.4.1.17
Reagents

Metabolite: InChI=1S/C23H27...

Sulfonation of phenolic compound BTMR1376
Enzimas: 2.8.2.1
Reagents

Metabolite: InChI=1S/C17H19...

Methylation of phenolic compound BTMR1377
Enzimas: 2.1.1.25
Hydroxylation of alicyclic secondary carbon BTMR1068
Reagents

Metabolite: InChI=1S/C17H19...

N-Oxidation of alicyclic tertiary amine BTMR1099
Reagents

Metabolite: InChI=1S/C17H19...

N-Dealkylation of alicyclic tertiary amine BTMR1144
Reagents

Metabolite: InChI=1S/C16H17...

Hydroxylation of heteroalicyclic secondary carbon BTMR1070
Reagents

Metabolite: InChI=1S/C17H19...

Hydroxylation of heteroalicyclic secondary carbon BTMR1071
Enzimas: CYP1A2
Reagents

Metabolite: InChI=1S/C17H19...

Hydroxylation of heteroalicyclic secondary carbon BTMR1071
Enzimas: CYP1A2
Reagents

Metabolite: InChI=1S/C17H19...

alpha-Hydroxylation of carbonyl group BTMR1054
Reagents

Metabolite: InChI=1S/C17H19...

Hydroxylation of alicyclic tertiary carbon BTMR1243
Enzimas: CYP1A2
Aliphatic hydroxylation of carbon alpha to secondary or tertiary alkyl-N BTMR1081
Reagents

Metabolite: InChI=1S/C17H19...

Aliphatic hydroxylation of carbon alpha to secondary or tertiary alkyl-N BTMR1081
Reagents

Metabolite: InChI=1S/C17H19...

Reduction of ketone to alcohol BTMR1171
Enzimas: CYP2C9
Reacciones que el metabolismo produce a partir de esta molécula
Dehydrogenation of secondary alcohol BTMR0030
Enzimas: 1.1.1.1
Oxidation of secondary alcohol to ketone BTMR0079
Products

Metabolite: InChI=1S/C17H21...

O-Dealkylation BTMR0052