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check_image( "../cid_images/cid_9410.png" ); ?>
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check_image( "../cid_thumbs/cid_3032993.png" ); ?>
check_image( "../cid_thumbs/cid_3032729.png" ); ?>
check_image( "../cid_thumbs/cid_3032728.png" ); ?>
check_image( "../cid_thumbs/cid_15135.png" ); ?>
check_image( "../cid_thumbs/cid_450882.png" ); ?>
check_image( "../cid_thumbs/cid_726644.png" ); ?>
check_image( "../cid_thumbs/cid_3537766.png" ); ?>
check_image( "../cid_thumbs/cid_62801.png" ); ?>
check_image( "../cid_thumbs/cid_4490157.png" ); ?>
check_image( "../cid_thumbs/cid_4518000.png" ); ?>
check_image( "../cid_thumbs/cid_126388.png" ); ?>
check_image( "../cid_thumbs/cid_118474.png" ); ?>
check_image( "../cid_thumbs/cid_2810801.png" ); ?>
check_image( "../cid_thumbs/cid_4107506.png" ); ?>
check_image( "../cid_thumbs/cid_4122144.png" ); ?>
check_image( "../cid_thumbs/cid_5799469.png" ); ?>
check_image( "../cid_thumbs/cid_34777.png" ); ?>
check_image( "../cid_thumbs/cid_1089.png" ); ?>
Uprima
PubChem Notes:
Apomorphine A derivative of morphine that is a dopamine D2 agonist. It is a powerful emetic and has been used for that effect in acute poisoning. It has also been used in the diagnosis and treatment of parkinsonism, but its adverse effects limit its use.
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pre_formula( "InChI=1/C17H17NO2.ClH/c1-18-8-7-10-3-2-4-12-15(10)13(18)9-11-5-6-14(19)17(20)16(11)12;/h2-6,13,19-20H,7-9H2,1H3;1H/t13-;/m1./s1", "jqp007/9410.html" ); ?>
Molecular Formula:
C17H18ClNO2
InChI: InChI=1/C17H17NO2.ClH/c1-18-8-7-10-3-2-4-12-15(10)13(18)9-11-5-6-14(19)17(20)16(11)12;/h2-6,13,19-20H,7-9H2,1H3;1H/t13-;/m1./s1
InChIKey: InChIKey=SKYZYDSNJIOXRL-BTQNPOSSBJ
SMILES: CN1CCC2=CC=CC3=C2C1CC4=C3C(=C(C=C4)O)O.Cl
Names:
Apokyn
Apomorphine chloride
Apomorphine HCl
Apomorphine hydrochloride
Apomorphine SL
Apomorphinium chloride
Apomorphinum hydrochloricum
Apomorphin hydrochlorid
pomorphini hydrochloridum
Uprima
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Registries:
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PubChem CID 9410
PubChem ID 152620
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require_once( "../ads.include" ); ?>
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