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check_image( "../cid_thumbs/cid_3583130.png" ); ?>
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check_image( "../cid_thumbs/cid_99983.png" ); ?>
check_image( "../cid_thumbs/cid_5356908.png" ); ?>
check_image( "../cid_thumbs/cid_6386182.png" ); ?>
check_image( "../cid_thumbs/cid_4476887.png" ); ?>
check_image( "../cid_thumbs/cid_30969.png" ); ?>
check_image( "../cid_thumbs/cid_9601043.png" ); ?>
check_image( "../cid_thumbs/cid_232507.png" ); ?>
check_image( "../cid_thumbs/cid_6316808.png" ); ?>
check_image( "../cid_thumbs/cid_3548001.png" ); ?>
check_image( "../cid_thumbs/cid_4792774.png" ); ?>
check_image( "../cid_thumbs/cid_3557842.png" ); ?>
check_image( "../cid_thumbs/cid_773909.png" ); ?>
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check_image( "../cid_thumbs/cid_6536992.png" ); ?>
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Tylciprine
PubChem Notes:
Tranylcypromine A propylamine formed from the cyclization of the side chain of amphetamine. This monoamine oxidase inhibitor is effective in the treatment of major depression, dysthymic disorder, and atypical depression. It also is useful in panic and phobic disorders. (From AMA Drug Evaluations Annual, 1994, p311)
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pre_formula( "InChI=1/2C9H11N.H2O4S/c2*10-9-6-8(9)7-4-2-1-3-5-7;1-5(2,3)4/h2*1-5,8-9H,6,10H2;(H2,1,2,3,4)/t2*8-,9+;/m10./s1/f2C9H12N.O4S/h2*10H;/q2*+1;-2", "jqp005/26069.html" ); ?>
Molecular Formula:
C18H24N2O4S
InChI: InChI=1/2C9H11N.H2O4S/c2*10-9-6-8(9)7-4-2-1-3-5-7;1-5(2,3)4/h2*1-5,8-9H,6,10H2;(H2,1,2,3,4)/t2*8-,9+;/m10./s1/f2C9H12N.O4S/h2*10H;/q2*+1;-2
InChIKey: InChIKey=BKPRVQDIOGQWTG-NZYVFOJUDV
SMILES: C1C(C1[NH3+])C2=CC=CC=C2.C1C(C1[NH3+])C2=CC=CC=C2.[O-]S(=O)(=O)[O-]
Names:
dl-Tranylcypromine sulfate
EINECS 236-807-1
Parnate
Phenylcyclopromine sulfate
trans,DL-2-Phenylcyclopropylamine sulfate
Tranylcypromine sulfate
Tranylcypromine sulphate
Tylciprine
(+-)-trans-2-Phenylcyclopropylamine sulfate (2:1)
1-Amino-2-phenylcyclopropane sulfate
[(1R,2R)-2-phenylcyclopropyl]azanium sulfate
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Registries:
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PubChem CID 26069
PubChem ID 168817
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require_once( "../ads.include" ); ?>
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