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Details

Stereochemistry ABSOLUTE
Molecular Formula C33H46O4
Molecular Weight 506.7159
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NANDROLONE P-HEXYLOXYPHENYLPROPIONATE

SMILES

[H][C@@]12CC[C@H](OC(=O)CCC3=CC=C(OCCCCCC)C=C3)[C@@]1(C)CC[C@]4([H])[C@@]5([H])CCC(=O)C=C5CC[C@@]24[H]

InChI

InChIKey=PQKRYXHYWWQULJ-JMKYFRMNSA-N
InChI=1S/C33H46O4/c1-3-4-5-6-21-36-26-12-7-23(8-13-26)9-18-32(35)37-31-17-16-30-29-14-10-24-22-25(34)11-15-27(24)28(29)19-20-33(30,31)2/h7-8,12-13,22,27-31H,3-6,9-11,14-21H2,1-2H3/t27-,28+,29+,30-,31-,33-/m0/s1

HIDE SMILES / InChI
Nandrolone hexyloxyphenylpropionate (brand names Anador, Anadur, Anadurine) is a synthetic androgen and anabolic steroid is marketed in some countries. Nandrolone, in general, is more anabolic than testosterone and has a very low androgenic expression. It is reported to have an anabolic to androgenic ratio of 37:125. Typically, males would take a dosage range of 200-600mg/wk with higher doses sometimes found in more advanced users. This compound normally would not be recommended for women due to the virilization effects this compound may cause such as increased body hair, deepened voice. Anadur has a high affinity towards the androgen receptor while having a lower androgenic expression, it is usually not recommended to be taken without testosterone. Without a high androgenic expression and having a strong bond to the AR, side effects of low testosterone are possible such as the infamous "Deca-Dick" (impotence), lethargy, and low sex drive.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct

Sample Use Guides

In Vivo Use Guide
Effective Dose (Men): 200-600 mgs/week (2mg/lb of Body weight); Effective Dose (Women): 50-100 mgs/week
Route of Administration: Intramuscular
In Vitro Use Guide
Unknown
Name Type Language
NANDROLONE P-HEXYLOXYPHENYLPROPIONATE
MI   WHO-DD  
Common Name English
17.BETA.-HYDROXYESTR-4-EN-3-ONE P-(HEXYLOXY)HYDROCINNAMATE
Common Name English
NORTESTOSTERONE (P-HEXYLOXYPHENYL)PROPIONATE
Common Name English
17.BETA.-HYDROXYESTR-4-EN-3-ONE P-HEXYLOXYPHENYLPROPIONATE
Common Name English
ESTR-4-EN-3-ONE, 17.BETA.-HYDROXY-, P-(HEXYLOXY)HYDROCINNAMATE
Common Name English
NANDROLONE P-HEXYLOXYPHENYLPROPIONATE [MI]
Common Name English
ANADUR
Brand Name English
NANDROLONE (P-HEXYLOXYPHENYL)PROPIONATE
Common Name English
19-NORTESTOSTERONE 3-(P-HEXYLOXYPHENYL)PROPIONATE
Common Name English
NHPP
Common Name English
ANADURINE
Brand Name English
Nandrolone p-hexyloxyphenylpropionate [WHO-DD]
Common Name English
17.BETA.-HYDROXY-19-NORANDROSTEN-4-EN-3-ONE P-HEXYLOXYPHENYLPROPIONATE
Common Name English
ANADOR
Brand Name English
NANDROLONE HEXYLOPHENYLPROPIONATE
Common Name English
ESTR-4-EN-3-ONE, 17-(3-(4-(HEXYLOXY)PHENYL)-1-OXOPROPOXY)-, (17.BETA.)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C2360
Created by admin on Fri Dec 15 19:02:08 GMT 2023 , Edited by admin on Fri Dec 15 19:02:08 GMT 2023
Code System Code Type Description
PUBCHEM
92341
Created by admin on Fri Dec 15 19:02:08 GMT 2023 , Edited by admin on Fri Dec 15 19:02:08 GMT 2023
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NCI_THESAURUS
C95971
Created by admin on Fri Dec 15 19:02:08 GMT 2023 , Edited by admin on Fri Dec 15 19:02:08 GMT 2023
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MERCK INDEX
m7720
Created by admin on Fri Dec 15 19:02:08 GMT 2023 , Edited by admin on Fri Dec 15 19:02:08 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID20966654
Created by admin on Fri Dec 15 19:02:08 GMT 2023 , Edited by admin on Fri Dec 15 19:02:08 GMT 2023
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WIKIPEDIA
Nandrolone hexyloxyphenylpropionate
Created by admin on Fri Dec 15 19:02:08 GMT 2023 , Edited by admin on Fri Dec 15 19:02:08 GMT 2023
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ECHA (EC/EINECS)
257-810-4
Created by admin on Fri Dec 15 19:02:08 GMT 2023 , Edited by admin on Fri Dec 15 19:02:08 GMT 2023
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CAS
52279-57-9
Created by admin on Fri Dec 15 19:02:08 GMT 2023 , Edited by admin on Fri Dec 15 19:02:08 GMT 2023
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SMS_ID
100000085690
Created by admin on Fri Dec 15 19:02:08 GMT 2023 , Edited by admin on Fri Dec 15 19:02:08 GMT 2023
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EVMPD
SUB03386MIG
Created by admin on Fri Dec 15 19:02:08 GMT 2023 , Edited by admin on Fri Dec 15 19:02:08 GMT 2023
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FDA UNII
602JJC2862
Created by admin on Fri Dec 15 19:02:08 GMT 2023 , Edited by admin on Fri Dec 15 19:02:08 GMT 2023
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